WO1992009690A2 - Enrichment method for variant proteins with altered binding properties - Google Patents
Enrichment method for variant proteins with altered binding properties Download PDFInfo
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- WO1992009690A2 WO1992009690A2 PCT/US1991/009133 US9109133W WO9209690A2 WO 1992009690 A2 WO1992009690 A2 WO 1992009690A2 US 9109133 W US9109133 W US 9109133W WO 9209690 A2 WO9209690 A2 WO 9209690A2
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- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
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- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
- G01N33/6803—General methods of protein analysis not limited to specific proteins or families of proteins
- G01N33/6845—Methods of identifying protein-protein interactions in protein mixtures
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- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
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- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/74—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving hormones or other non-cytokine intercellular protein regulatory factors such as growth factors, including receptors to hormones and growth factors
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- C07K2319/02—Fusion polypeptide containing a localisation/targetting motif containing a signal sequence
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- C07K2319/70—Fusion polypeptide containing domain for protein-protein interaction
- C07K2319/735—Fusion polypeptide containing domain for protein-protein interaction containing a domain for self-assembly, e.g. a viral coat protein (includes phage display)
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- C07K2319/70—Fusion polypeptide containing domain for protein-protein interaction
- C07K2319/74—Fusion polypeptide containing domain for protein-protein interaction containing a fusion for binding to a cell surface receptor
- C07K2319/75—Fusion polypeptide containing domain for protein-protein interaction containing a fusion for binding to a cell surface receptor containing a fusion for activation of a cell surface receptor, e.g. thrombopoeitin, NPY and other peptide hormones
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- C12N2750/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA ssDNA viruses
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- C12N2795/00—Bacteriophages
- C12N2795/00011—Details
- C12N2795/14011—Details ssDNA Bacteriophages
- C12N2795/14022—New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes
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- C12N2795/00—Bacteriophages
- C12N2795/00011—Details
- C12N2795/14011—Details ssDNA Bacteriophages
- C12N2795/14111—Inoviridae
- C12N2795/14122—New viral proteins or individual genes, new structural or functional aspects of known viral proteins or genes
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/435—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans
- G01N2333/575—Hormones
- G01N2333/61—Growth hormones [GH] (Somatotropin)
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S436/00—Chemistry: analytical and immunological testing
- Y10S436/802—Protein-bacteriophage conjugates
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S930/00—Peptide or protein sequence
- Y10S930/01—Peptide or protein sequence
- Y10S930/12—Growth hormone, growth factor other than t-cell or b-cell growth factor, and growth hormone releasing factor; related peptides
Definitions
- This invention relates to the preparation and systematic selection of novel binding proteins having altered binding properties for a target molecule. Specifically, this invention relates to methods for producing foreign poiypeptides mimicking the binding activity of naturally occurring binding partners, in preferred embodiments, the invention is directed to the preparation of therapeutic or diagnostic compounds that mimic proteins or nonpeptidyl molecules such a hormones, drugs and other small molecules, particularly biologically active molecules such as growth hormone.
- Binding partners are substances that specifically bind to one another, usually through noncovalent interactions. Examples of binding partners include iigand-receptor, antibody-antigen, drug-target, and enzyme- substrate interactions. Binding partners are extremely useful in both therapeutic and diagnostic fields. Binding partners have been produced in the past by a variety of methods including; harvesting them from nature (e.g., antibody-antigen, and Iigand-receptor pairings) and by adventitious identification (e.g. traditional drug development employing random screening of candidate molecules). In some instances these two approaches have been combined. For example, variants of proteins or poiypeptides, such as polypeptide fragments, have been made that contain key functional residues that participate in binding. These polypeptide fragments, in turn, have been derivatized by methods akin to traditional drug development. An example of such derivitization would include strategies such as cyclization to conformationally constrain a polypeptide fragment to produce a novel candidate binding partner.
- Geysen In an attempt to overcome these problems, Geysen (Geysen, Immun. Today.6:364-369 [1985]); and (Geysen et al., ol. Immun..23:709-715 [1986]) has proposed the use of polypeptide synthesis to provide a framework for systematic iterative binding partner identification and preparation. According to Geysen et al., Ibid, short poiypeptides, such as dipeptides, are first screened for the ability to bind to a target molecule.
- the most active dipeptides are then selected for an additional round of testing comprising linking, to the starting dipeptide, an additional residue (or by internally modifying the components of the original starting dipeptide) and then screening this set of candidates for the desired activity. This process is reiterated until the binding partner having the desired properties is identified.
- the Geysen etal. method suffers from the disadvantage that the chemistry upon which it is based, peptide synthesis, produces molecules with ill-defined or variable secondary and tertiary structure.
- random interactions accelerate among the various substituent groups of the polypeptide so that a true random population of interactive molecules having reproducible higher order structure becomes less and less attainable.
- interactions between side chains of amino acids, which are sequentially widely separated but which are spatially neighbors freely occur.
- sequences that do not facilitate conformationally stable secondary structures provide complex peptide-sidechain interactions which may prevent sidechain interactions of a given amino acid with the target molecule. Such complex interactions are facilitated by the flexibility of the polyamide backbone of the polypeptide candidates.
- candidates may exist in numerous conformations making it difficult to identify the conformer that interacts or binds to the target with greatest affinity or specificity complicating rational drug design.
- a final problem with the iterative polypeptide method of Geysen is that, at present, there are no practical methods with which a great diversity of different peptides can be produced, screened and analyzed.
- the total number of all combinations of hexapeptides that must be synthesized is 64,000,000.
- Even having prepared such a diversity of peptides there are no methods available with which mixtures of such a diversity of peptides can be rapidly screened to select those peptides having a high affinity for the target molecule.
- each 'adherent * peptide must be recovered in amounts large enough to carry out protein sequencing.
- biological selection and screening was chosen as an alternative.
- fusion phage * there are, however, several important limitations in using such "fusion phage * to identify altered peptides or proteins with new or enhanced binding properties.
- prior art methods have been unable to select peptides from a library having the highest binding affinity for a target molecule.
- Ladner WO 9002802 discloses a method for selecting novel binding proteins displayed on the outer surface of cells and viral particles where it is contemplated that the heterologous proteins may have up to 164 amino acid residues .
- the method contemplates isolating and amplifying the displayed proteins to engineer a new family of binding proteins having desired affinity for a target molecule. More specifically, Ladner discloses a 'fusion phage * displaying proteins having 'initial protein binding domains' ranging from 46 residues (crambin) to 164 residues (T4 lysozyme) fused to the M13 gene III coat protein. Ladner teaches the use of proteins "no larger than necessary" because it is easier to arrange restriction sites in smaller amino acid sequences and prefers the 58 amino acid residue bovine pancreatic trypsin inhibitor (BPTI).
- BPTI pancreatic trypsin inhibitor
- BPTI small fusion proteins
- T4 lysozyme small target molecules
- small target molecules such as steroids
- the preferred protein, BPTI is proposed to be fused to gene III at the site disclosed by Smith et al. or de la Cruz et al., J. Biol. Chem..263: 43184322 [1988], or to one of the terminii, along with a second synthetic copy of gene III so that "some" unaltered gene III protein will be present. Ladner does not address the problem of successfully panning high affinity peptides from the random peptide library which plagues the biological selection and screening methods of the prior ait
- hGH Human growth hormone
- hGH is a member of a family of homologous hormones that include placental Iactogens, prolactins, and other genetic and species variants or growth hormone (Nicoll, C. S., etal., (I986) Endocrine Reviews 7. 169). hGH is unusual among these in that it exhibits broad species specificity and binds to either the cloned somatogenic (Leung, D. W., etal., [I987] Nature 330. 537) or prolactin receptor (Boutin, J. M.,ef a/., [I988] Q ⁇ ⁇ 1 69).
- the cloned gene for hGH has been expressed in a secreted form in Escherichia &U (Chang, C. N., et al., ⁇ Qs ⁇ s.55, 189) and its DNA and amino acid sequence has been reported (Goeddel, ef al., [I979] iE£ 2S1 544; Gray, et al., [I985] Gene 3J 247).
- the three-dimensional structure of hGH is not available. However, the three-dimensional folding pattern for porcine growth hormone (pGH) has been reported at moderate resolution and refinement (Abdel-Meguid, S. S., etal., [1987] Proc. Natl. Acad. Sci. USA 84.
- hGH Human growth hormone
- It is another object of this invention to prepare candidate binding substances comprising fusion proteins of a phage coat protein and a heterologous polypeptide where the polypeptide is greater than 100 amino acids in length and may be more than one subunit and is displayed on a phagemid particle where the polypeptide is encoded by the phagemid genome.
- Still another object of the invention is the production of growth hormone variants that exhibit stronger affinity for growth hormone receptor and binding protein.
- a method for selecting novel binding poiypeptides comprising: (a) constructing a replicable expression vector comprising a first gene encoding a polypeptide, a second gene encoding at least a portion of a natural or wild-type phage coat protein wherein the first and second genes are heterologous, and a transcription regulatory element operabfy linked to the first and second genes, thereby forming a gene fusion encoding a fusion protein; (b) mutating the vector at one or more selected positions within the first gene thereby forming a family of related plasmids; (c) transforming suitable host cells with the plasmids; (d) infecting the transformed host cells with a helper phage having a gene encoding the phage coat protein; (e) culturing the transformed infected host cells under conditions suitable for forming recombinant phagemid particles containing at least a portion of the plasmid
- the method for selecting novel binding proteins where the proteins are composed of more than one subunit is achieved by selecting novel binding peptides comprising constructing a replicable expression vector comprising a transcription regulatory element operabfy linked to DNA encoding a protein of interest containing one or more subunits, wherein the DNA encoding at least one of the subunits is fused to the DNA encoding at least a portion of a phage coat protein;mutating the DNA encoding the protein of interest at one or more selected positions thereby forming a family of related vectors; transforming suitable host cells with the vectors; infecting the transformed host cells with a helper phage having a gene encoding the phage coat protein; culturing the transformed infected host cells under conditions suitable for forming recombinant phagemid particles containing at least a portion of the plasmid and capable of transforming the host, the conditions adjusted so that no more than a minor amount of phagemid particles display more than one copy of the fusion protein on the
- the plasmid is under tight control of the transcription regulatory element, and the culturing conditions are adjusted so that the amount or number of phagemid particles displaying more than one copy of the fusion protein on the surface of the particle is less than about 1 %. Also preferably, amount of phagemid particles displaying more than one copy of the fusion protein is less than 10% the amount of phagemid particles displaying a single copy of the fusion protein. Most preferably the amount is less than 20%.
- the expression vector will further contain a secretory signal sequences fused to the DNA encoding each subunit of the polypeptide, and the transcription regulatory element will be a promoter system.
- Preferred promoter systems are selected from; Lac Z, ⁇ p
- the first gene will encode a mammalian protein, preferably the protein will be selected from; human growth hormone(hGH), N-methionyl human growth hormone, bovine growth hormone, parathyroid hormone, thyroxine, insulin A-chain, insulin B-chain, proinsulin, relaxin A-chain, relaxin B-chain, proretaxin, glycoprotein hormones such as follicle stimulating hormone(FSH), thyroid stimulating hormone(TSH), and leutinizing hormone(LH), glycoprotein hormone receptors, calcitonin, glucagon, factor VIII, an antibody, lung surfactant, urokinase, streptokinase, human tissue-type plasminogen activator (t-PA), bo besin, factor IX, thro bin, hemopoiet ' ic growth factor, tumor necrosis factor-alpha and -beta, enkephalinase, human serum albumin, mullerian-inhibiting substance, mouse gonadotropin-associated
- the first gene will encode a polypeptide of one or more subunits containing more than about 100 amino acid residues and will be folded to form a plurality of rigid secondary structures displaying a plurality of amino acids capable of interacting with the target.
- the first gene will be mutated at codons corresponding to only the amino acids capable of interacting with the target so that the integrity of the rigid secondary structures will be preserved.
- helper phage selected from; 13K07, M13R408, M13-VCS, and Phi X 174.
- the preferred helper phage is M13K07
- the preferred coat protein is the M13 Phage gene III coat protein.
- the preferred host is £ coli, and protease deficient strains of £ coli. Novel hGH variants selected by the method of the present invention have been detected.
- Phagemid expression vectors were constructed that contain a suppressible termination codon functionally located between the nucleic acids encoding the polypeptide and the phage coat protein.
- FIGURE 1 Strategy for displaying large proteins on the surface of filamentous phage and enriching for altered receptor binding properties.
- a plasmid, phGH-M13glll was constructed that fuses the entire coding sequence of hGH to the carboxyl terminal domain of M13 gene III. Transcription of the fusion protein is under control of the lac promoter/operator sequence, and secretion is directed by the stll signal sequence.
- Phagemid particles are produced by infection with the "helper * phage, M13K07, and particles displaying hGH can be enriched by binding to an affinity matrix containing the hGH receptor.
- the wild-type gene III (derived from the M13K07 phage) is diagramed by 4-5 copies of the multiple arrows on the tip of the phage, and the fusion protein (derived from the phagemid, phGH-M13glll) is indicated schematically by the folding diagram of hGH replacing the arrowhead.
- FIGURE 2 Immunoblot of whole phage particles shows that hGH comigrates with phage.
- Phagemid particles purified in a cesium chloride gradient were loaded into duplicate wells and electrophoresed through a 1 % agarose gel in 375 M Tris, 40 mM glycine pH 9.6 buffer. The gel was soaked in transfer buffer (25 mM Tris, pH 8.3, 200 mM glycine, 20% methanol) containing 2% SDS and 2% ⁇ -mercaptoethanol for 2 hours, then rinsed in transfer buffer for 6 hours. The proteins in the gel were then electrobfotted onto immobilon membranes (Millipore).
- the membrane containing one set of samples was stained with Coomassie blue to show the position of the phage proteins (A).
- the duplicate membrane was immuno-stained for hGH by reacting the membrane with polyclonal rabbit anti-hGH antibodies followed by reaction with horseradish peroxidase conjugated goat anti- rabbit IgG antibodies (B).
- Lane 1 contains the M13K07 parent phage and is visible only in the Coomassie blue stained membrane, since it lacks hGH.
- Lanes 2 and 3 contain separate preparations of the hormone phagemid particles which is visible both by Coomassie and hGH immuno-staining.
- the difference in migration distance between the parent M13K07 phage and hormone phagemid particles reflects the different size genomes that are packaged within (8.7 kb vs.5.1 kb, respectively).
- FIGURE 3 Summary diagram of steps in the selection process for an hGH-phage library randomized at codons 172, 174, 176, and 178.
- the template molecules, pH0415, containing a unique Kpnl restriction site and the hGH(R178G,H79T) gene was mutagenized as described in the text and electrofransformed into £ coli strain WJM101 to obtain the initial phagemid library, Library 1.
- An aliquot (approximately 2%) from Library 1 was used directly in an initial selection round as described in the text to yield Library 1G.
- dsDNA double-stranded DNA
- Library I double-stranded DNA
- Kpnl restriction enzyme
- phagemid propagation were carried out as indicated by the arrows, according to the procedure described in the text.
- Four independent clones from Library 4G 4 and four independent clones from Library 5G 6 were sequenced by dideoxy sequencing. All of these clones had the identical DNA sequence, corresponding to the hGH mutant (Glu 174 Ser, Phe 176 Tyr).
- FIGURE 4 Structural model of hGH derived from a 2.8 A folding diagram of porcine growth hormone determined crystallographically. Location of residues in hGH that strongly modulate its binding to the hGH- binding protein are within the shaded circle. Alanine substitutions that cause a greater than tenfold reduction ⁇ ), a four- to tenfold reduction (•), or increase (O), or a two- to fourfold reduction (•), in binding affinity are indicated.
- Helical wheel projections in the regions of ⁇ -helix reveal their amphipathic quality. Blackened, shaded, or nonshaded residues are charged, polar, or nonpolar, respectively. In helix-4 the most important residues for mutation are on the hydrophilic face.
- FIGURE 5 Amino acid substitutions at positions 172, 174, 176 and 178 of hGH (The notation, e.g. KSYR, denotes hGH mutant 172K 174S/176Y/178R.) found after sequencing a number of clones from rounds 1 and 3 of the selection process for the pathways indicated (hGH elution; Glycine elution; or Glycine elution after pre-adsorption).
- Non-functional sequences i.e. vector background, or other prematurely terminated and/or frame-shifted mutants
- Functional sequences which contained a non-silent, spurious mutation i.e. outside the set of target residues
- Protein sequences which appeared more than once among all the sequenced clones, but with different DNA sequences, are marked with a "#". Protein sequences which appeared more than once among the sequenced clones and with the same DNA sequence are marked with a "”. Note that after three rounds of selection, 2 different contaminating sequences were found; these clones did not correspond to cassette mutants, but to previously constructed hormone phage. The pS0643 contaminant corresponds to wild-type hGH-phage (hGH "KEFR").
- the pH0457 contaminant which dominates the third- round glycine-selected pool of phage, corresponds to a previously identified mutant of hGH, "KSYR.”
- K a previously identified mutant of hGH
- the amplification of these contaminants emphasizes the ability of the hormone-phage selection process to select for rarely occurring mutants.
- the convergence of sequences is also striking in all three pathways: R or K occurs most often at positions 172 and 178; Y or F occurs most often at position 176; and S, T, A, and other residues occur at position 174.
- FIGURE 6 Sequences from phage selected on hPRLbp-beads in the presence of zinc. The notation is as described in Figure.5. Here, the convergence of sequences is not predictable, but there appears to be a bias towards hydrophobic sequences under the most stringent (Glycine) selection conditions; L ,W and P residues are frequently found in this pool.
- FIGURE 7 Sequences from phage selected on hPRLbp-beads in the absence of zinc. The notation is as described in Figure 5. In contrast to the sequences of Figure.6, these sequences appear more hydrophilic. After 4 rounds of selection using hGH elution, two clones (ANHQ, and TLDT/171 V) dominate the pool.
- FIGURE 8 Sequences from phage selected on blank beads. The notation is as described in Fig.5. After three rounds of selection with glycine elution, no siblings were observed and a background level of non-functional sequences remained.
- FIGURE 9 Construction of phagemid fl ori from pH0415.
- This vector for cassette mutagenesis and expression of the hGH-gene III fusion protein was constructed as follows. Plasmid pS0643 was constructed by oligonucleotide-directed mutagenesis of pS0132, which contains pBR322 and f1 origins of replication and expresses an hGH-gene III fusion protein (hGH residues 1-191, followed by a single Giy residue, fused to Pro-198 of gene III) under the control of the E. coli phoA promoter.
- FIGURE 10 A. Diagram of plasmid pDH188 insert containing the DNA encoding the light chain and heavy chain (variable and constant domain 1 ) of the Fab humanized antibody directed to the HER-2 receptor.
- _ and VH are the variable regions for the light and heavy chains, respectively.
- is the constant region of the human kappa light chain.
- CH1Q1 is the first constant region of the human gamma 1 chain. Both coding regions start with the bacterial st II signal sequence.
- B A schematic diagram of the entire plasma pDH188 containing the insert described in 5A. After transformation of the plasmid into £ coli SR101 cells and the addition of helper phage, the plasmid is packaged into phage particles. Some of these particles display the Fab-p HI fusion (where p III is the protein encoded by the M13 gene III DNA). The segments in the plasmid figure correspond to the insert shown in5A.
- FIGURE 11 A through C are collectively referred to here as Figure 11.
- the amino acid sequence of the light chain is also shown (Seq. ID No.26), as is the amino acid sequence of the heavy chain p ill fusion (Seq. ID No. 27).
- FIGURE 12 Enrichment of wild-type 4D5 F a b phagemid from variant F a b phagemid.
- Mixtures of wild- type phagemid and variant 4D5 Fab phagemid in a ratio of 1 :1 ,000 were selected on plates coated with the extra- cellular domain protein of the HER-2 receptor. After each round of selection, a portion of the eluted phagemid were infected into £ coli and plasmid DNA was prepared. This plasmid DNA was then digested with Eco RV and Pst I, separated on a 5% polyacrylamide gel, and stained with ethidium bromide. The bands were visualized under UV light.
- the bands due to the wild-type and variant plasmids are marked with arrows.
- the first round of selection was eluted only under acid conditions; subsequent rounds were eluted with either an add elution (left side of Figure) or with a humanized 4D5 antibody wash step prior to acid elution (right side of Figure) using methods described in Example VIII.
- H91 A amino acid histidine at position 91 on the V chain mutated to alanine; indicated as 'A' lanes in Figure
- Y49A amino acid tyrosine at position 49 on the V chain mutated to alanine; indicated as 'B' lanes in the Figure
- Y92A amino acid tyrosine at position 92 on the V chain mutated to alanine; indicated as "C lanes in the Figure.
- Amino acid position numbering is according to Kabat et al.,(Sequences of proteins of immunological interest, 4th ed., U.S. Dept of Health and Human Services, Public Health Service, Nat'l. Institute of Health, Bethesda, MD [1987]).
- FIGURE 13 The Scatchard analysis of the RIA affinity determination described in Experimental Protocols is shown here.
- the amount of labeled ECD antigen that is bound is shown on the x-axis while the amount that is bound divided by the amount that is free is shown on the y-axis.
- the slope of the line indicates the Ka; the calculated Kd is VK-, DETAILED DESCRIPTION OF THE INVENTION
- the method of the instant invention comprises a method for selecting novel binding poiypeptides, such as protein ligands, having a desired, usually high, affinity for a target molecule from a library of structurally related binding poiypeptides.
- the library of structurally related poiypeptides, fused to a phage coat protein, is produced by mutagenesis and, preferably, a single copy of each related polypeptide is displayed on the surface of a phagemid particle containing DNA encoding that polypeptide.
- These phagemid particles are then contacted with a target molecule and those particles having the highest affinity for the target are separated from those of lower affinity.
- the high affinity binders are then amplified by infection of a bacterial host and the competitive binding step is repeated. This process is reiterated until poiypeptides of the desired affinity are obtained.
- novel binding poiypeptides or ligands produced by the method of this invention are useful per se as diagnostics or therapeutics (eg. agonists or antagonists) used in treatment of biological organisms. Structural analysis of the selected poiypeptides may also be used to facilitate rational drug design.
- binding polypeptide as used herein is meant any polypeptide that binds with a selectable affinity to a target molecule.
- the polypeptide will be a protein that most preferably contains more than about 100 amino acid residues.
- the polypeptide will be a hormone or an antibody or a fragment thereof.
- high affinity * as used herein is meant an affinity constant (Kd ) of ⁇ 10 "5 M and preferably ⁇ 10 "7 M under physiological conditions.
- target molecule as used herein is meant any molecule, not necessarily a protein, for which it is desirable to produce a ligand.
- the target will be a protein and most preferably the target will be a receptor, such as a hormone receptor.
- humanized antibody as used herein is meant an antibody in which the complementarity-determining regions (CDRs) of a mouse or other non-human antibody are grafted onto a human antibody framework.
- human antibody framework is meant the entire human antibody excluding the CDRs. L Choice of Pohmeptktes for Display on the Surface of a Phage
- the first step in the method of this invention is to choose a polypeptide having rigid secondary structure exposed to the surface of the polypeptide for display on the surface of a phage.
- polypeptide as used herein is meant any molecule whose expression can be directed by a specific DNA sequence.
- the poiypeptides of this invention may comprise more than one subunit, where each subunit is encoded by a separate DNA sequence.
- rigid secondary structure as used herein is meant any polypeptide segment exhibiting a regular repeated structure such as is found in; ⁇ -helices, 3 ⁇ o helices, ⁇ -helices, parallel and antiparallel ⁇ -sheets, and reverse turns.
- Certain "non-ordered" structures that lack recognizable geometric order are also included in the definition of rigid secondary structure provided they form a domain or "patch" of amino acid residues capable of interaction with a target and that the overall shape of the structure is not destroyed by replacement of an amino acid within the structure . It is believed that some non-ordered structures are combinations of reverse turns.
- the geometry of these rigid secondary structures is well defined by ⁇ and ⁇ torsional angles about the ⁇ -carbons of the peptide "backbone”.
- the requirement that the secondary structure be exposed to the surface of the polypeptide is to provide a domain or 'patch' of amino acid residues that can be exposed to and bind with a target molecule. It is primarily these amino acid residues that are replaced by mutagenesis that form the 'library * of structurally related (mutant) binding poiypeptides that are displayed on the surface of the phage and from which novel polypeptide ligands are selected. Mutagenesis or replacement of amino acid residues directed toward the interior of the polypeptide is generally avoided so that the overall structure of the rigid secondary structure is preserved.
- Example VIII phagemid selection of hGH was conducted in cycles.
- amino acids 172, 174, 176 and 178 were mutated and phagemid selected.
- amino acids 167, 171, 175 and 179 were phagemid selected.
- hGH amino acids 10, 14, 18 and 21 were phagemid selected.
- Optimum amino acid changes from a previous cycle may be incorporated into the polypeptide before the next cycle of selection. For example, hGH amino acids substitution 174 (serine) and 176 (tyrosine) were incorporated into the hGH before the phagemid selection of hGH amino acids 167, 171, 175 and 179.
- the amino acid residues that form the binding domain of the polypeptide will not be sequentially linked and may reside on different subunits of the polypeptide. That is, the binding domain tracks with the particular secondary structure at the binding site and not the primary structure.
- mutations will be introduced into codons encoding amino acids within a particular secondary structure at sites directed away from the interior of the polypeptide so that they will have the potential to interact with the target.
- Figure 2 shows the location of residues in hGH that are known to strongly modulate its binding to the hGH-binding protein (Cunningham etal., Science 247:1461 - 1465 [1990]).
- a glycoprotein hormone such as TSH can be chosen as a ligand for the FSH receptor and a library of mutant TSH molecules are employed in the method of this invention to produce novel drug candidates.
- Preferred poiypeptides are those that have pharmaceutical utility. More preferred poiypeptides include; a growth hormone, including human growth hormone, des-N-methionyl human growth hormone, and bovine growth hormone; parathyroid hormone; thyroid stimulating hormone; thyroxine; insulin A-chain; insulin B-chain; proinsulin; follicle stimulating hormone; calcitonin; leutinizing hormone; glucagon; factor VIII; an antibody; lung surfactant; a plasminogen activator, such as urokinase or human tissue-type plasminogen activator (t-PA); bombesin; factor IX, thrombi ⁇ ; hemopoietic growth factor; tumor necrosis factor-alpha and -beta;enkephalinase; a serum albumin such as human serum albumin; mullerian-inhibiting substance; relaxin A-chain; relaxin B-chain
- one or more predetermined amino acid residues on the polypeptide may be substituted, inserted, or deleted, for example, to produce products with improved biological properties.
- fragments of these poiypeptides, especially biologically active fragments are included.
- Yet more preferred poiypeptides of this invention are human growth hormone , and atrial naturetic peptides A, B, and C, endotoxin, subtilisin, trypsin and other serine proteases.
- polypeptide hormones that can be defined as any amino acid sequence produced in a first cell that binds specifically to a receptor on the same cell type (autocrine hormones) or a second cell type (non-autocrine) and causes a physiological response characteristic of the receptor-bearing cell.
- polypeptide hormones include cytokines, lymphokines, neurotrophic hormones and adenohypophyseal polypeptide hormones such as growth hormone, proJactin, placental lactogen, luteinizing hormone, follicle-stimulating hormone, thyrotropin, chorionic gonadotropin, cor ⁇ cotropin, ⁇ or ⁇ -melanocyte-stimulating hormone, ⁇ -iipotropin, ⁇ - lipotropin and the endorphins; hypothal ic release-inhibiting hormones such as corticotropin-release factor, growth hormone release-inhibiting hormone, growth hormone-release factor; and other polypeptide hormones such as atrial natriuretic peptides A, B or C.
- cytokines fGene ii encoding the desired polvpeotide
- the gene encoding the desired polypeptide i.e., a polypeptide with a rigid secondary structure
- the DNA encoding the gene may be chemically synthesized (Merrfield, J. Am. Chem. Soc...85 2149 [1963]).
- the sequence of the gene is not known, or if the gene has not previously been isolated, it may be cloned from a cDNA library (made from RNA obtained from a suitable tissue in which the desired gene is expressed) or from a suitable genomic DNA library.
- probes include monoclonal or polyclonal antibodies (provided that the cDNA library is an expression library), oligonucleotides, and complementary or homologous cDNAs or fragments thereof.
- the probes that may be used to isolate the gene of interest from genomic DNA libraries include cDNAs or fragments thereof that encode the same or a similar gene, homologous genomic DNAs or DNA fragments, and oligonucleotides. Screening the cDNA or genomic library with the selected probe is conducted using standard procedures as described in chapters 10-12 of Sambrook etal., supra.
- PCR polymerase chain reaction methodology
- Plasmid vectors are the preferred vectors for use herein, as they may be constructed with relative ease, and can be readily amplified. Plasmid vectors generally contain a variety of components including promoters, signal sequences, phenotypic selection genes, origin of replication sites, and other necessary components as are known to those of ordinary skill in tiie art.
- Promoters most commonly used in prokaryotic vectors include the lac Z promoter system, the alkaline phosphatase ⁇ ⁇ ⁇ A promoter, the bacteriophage ⁇ PL promoter (a temperature sensitive promoter), the lac promoter (a hybrid irj_-J2£ promoter that is regulated by the lac repressor), the tryptophan promoter, and the bacteriophage T7 promoter.
- the lac Z promoter system the alkaline phosphatase ⁇ ⁇ ⁇ A promoter
- the bacteriophage ⁇ PL promoter a temperature sensitive promoter
- the lac promoter a hybrid irj_-J2£ promoter that is regulated by the lac repressor
- tryptophan promoter a hybrid irj_-J2£ promoter that is regulated by the lac repressor
- the tryptophan promoter a hybrid irj_-J2£ promoter that is regulated by the lac repressor
- Preferred promoters tor practicing this invention are those that can be tightly regulated such that expression of the fusion gene can be controlled. It is believed that the problem that went unrecognized in the prior art was that display of multiple copies of the fusion protein on the surface of the phagemid particle lead to multipoint attachment of the phagemid with the target It is believed this effect, referred to as the 'chelate effect", results in selection of false "high affinity" poiypeptides when multiple copies of the fusion protein are displayed on the phagemid particle in close proximity to one another so that the target was "chelated*. When multipoint attachment occurs, the effective or apparent Kd may be as high as the product of the individual Kds for each copy of the displayed fusion protein. This effect may be the reason Cwiria and coworkers supra were unable to separate moderate affinity peptides from higher affinity peptides.
- Preferred promoters used to practice this invention are the lac Z promoter and the ⁇ ba A promoter.
- the lac Z promoter is regulated by the lac repressor protein lac >. and thus transcription of the fusion gene can be controlled by manipulation of the level of the lac repressor protein.
- the phagemid containing the lac Z promoter is grown in a cell strain that contains a copy of the lac i repressor gene, a repressor for the l2£ Z promoter.
- Exemplary cell strains containing the laci gene include JM 101 and XL1-biue.
- the host cell can be cotransfected with a plasmid containing both the repressor lac i and the lac Z promoter.
- phagmide particles containing the lac Z promoter are grown in cell strains containing the lac i gene and the cell strains are cotransfected with a plasmid containing both the lac Z and lac i genes.
- an inducer such as isopropylthiogalactoside (IPTG).
- IPTG isopropylthiogalactoside
- the number of fusion proteins per phagemid particle is about 0.1 (number of bulk fusion proteins number of phagemid particles).
- the most preferred promoter used to practice this invention is ⁇ A. This promoter is believed to be regulated by the level of inorganic phosphate in the cell where the phosphate acts to down-regulate the activity of the promoter. Thus, by depleting cells of phosphate, the activity of the promoter can be increased. The desired result is achieved by growing cells in a phosphate enriched medium such as 2YT or LB thereby controlling the expression of the gene III fusion.
- One other useful component of vectors used to practice this invention is a signal sequence.
- This sequence is typically located immediately 5' to the gene encoding the fusion protein, and will thus be transcribed at the amino terminus of the fusion protein. However, in certain cases, the signal sequence has been demonstrated to be located at positions other 5' to the gene encoding the protein to be secreted. This sequence targets the protein to which it is attached across the inner membrane of the bacterial cell.
- the DNA encoding the signal sequence may be obtained as a restriction endonuclease fragment from any gene encoding a protein that has a signal sequence.
- Suitable prokaryotic signal sequences may be obtained from genes encoding, for example, LamB or OmpF (Wong etal., Gene.68:193 [1983]), MalE, PhoA and other genes.
- a preferred prokaryotic signal sequence for practicing this invention is the £ coli heat-stable enterotoxin II (STII) signal sequence as described by Chang ef al. , Gene. 55: 189 [1987].
- STII enterotoxin II
- phenotypic selection genes are those encoding proteins that confer antibiotic resistance upon the host cell.
- ampicillin resistance gene (amp) the ampicillin resistance gene (amp)
- lei tetracycline resistance gene
- Suitable vectors comprising the aforementioned components as well as the gene encoding the desired polypeptide (gene 1) are prepared using standard recombinant DNA procedures as described in Sambrook ef al. supra. Isolated DNA fragments to be combined to form the vector are cleaved, tailored, and ligated together in a specific order and orientation to generate the desired vector.
- the DNA is cleaved using the appropriate restriction enzyme or enzymes in a suitable buffer.
- a suitable buffer In general, about 0.2-1 ⁇ g of plasmid or DNA fragments is used with about 1-2 units of the appropriate restriction enzyme in about 20 ⁇ l of buffer solution.
- Appropriate buffers, DNA concentrations, and incubation times and temperatures are specified by the manufacturers of the restriction enzymes. Generally, incubation times of about one or two hours at 37'C are adequate, although several enzymes require higher temperatures. After incubation, the enzymes and other contaminants are removed by extraction of the digestion solution with a mixture of phenol and chloroform, and the DNA is recovered from the aqueous fraction by precipitation with ethanol.
- the ends of the DNA fragments must be compatible with each other. In some cases, the ends will be directly compatible after endonuclease digestion. However, it may be necessary to first convert the sticky ends commonly produced by endonuclease digestion to blunt ends to make them compatible for ligation. To blunt the ends, the DNA is treated in a suitable buffer for at least 15 minutes at 15'C with 10 units of of the Klenow fragment of DNA polymerase I (Klenow) in the presence of the four deoxynucleotide triphosphates. The DNA is then purified by phenol-chloroform extraction and ethanol precipitation.
- the cleaved DNA fragments may be size-separated and selected using DNA gel electrophoresis.
- the DNA may be electrophoresed through either an agarose or a polyacryiamide matrix. The selection of the matrix will depend on the size of the DNA fragments to be separated.
- the DNA is extracted from the matrix by electroelution, or, if low-melting agarose has been used as the matrix, by melting the agarose and extracting the DNA from it, as described in sections 6.30-6.33 of Sambrook et al., supra.
- the DNA fragments that are to be ligated together are put in solution in about equimolar amounts.
- the solution will also contain ATP, ligase buffer and a ligase such as T4 DNA ligase at about 10 units per 0.5 ⁇ g of DNA.
- the vector is at first linearized by cutting with the appropriate restriction endonuclease(s).
- the linearized vector is then treated with alkaline phosphatase or calf intestinal phosphatase. The phosphatasing prevents seiHigation of the vector during the ligation step.
- Prokaryotes are the preferred host cells for this invention.
- Suitable prokaryotic host cells include £ coli strain JM101, £ coli K12 strain 294 (ATCC number 31,446), £ coli strain W3110 (ATCC number 27,325), £ coli X1776 (ATCC number 31, 537), E.coli XL-1 Blue (stratagene), and E coli B; however many other strains of £ coli, such as HB101, NM522, NM538, NM539, and many other species and genera of prokaryotes ma be used as well.
- bacilli such as Bacillus subtilis.
- enterobacteriaceae such as Salmonella typ mu ⁇ um or Serratia marasa ⁇ s, and various Pseudomonas species mayaii be used as hosts. Transformation of prokaryotic cells is readily accomplished using the calcium chloride method as described in section 1.82 of Sambrook et al., supra. Alternatively, electroporation (Neumann ef al., EMBO J.. 1:841 [1982]) may be used to transform these cells. The transformed cells are selected by growth on an antibiotic, commonly tetracycline (tet) or ampicillin (amp), to which they are rendered resistant due to the presence of tet and/or amp resistance genes on the vector.
- an antibiotic commonly tetracycline (tet) or ampicillin (amp)
- Plasmid DNA can be isolated using methods known in the art. Two suitable methods are the small scale preparation of DNA and the large-scale preparation of DNA as described in sections 1.25-1.33 of Sambrook et al, supra. The isolated DNA can be purified by methods known in the art such as that described in section 1.40 of Sambrook ef al., supra. This purified plasmid DNA is then analyzed by restriction mapping andor DNA sequencing. DNA sequencing is generally performed by either the method of Messing et al. Nucleic Acids Res..9 * 309 [1981] or by the method of Maxam etal. Meth. Enzymol..65: 499 [1980]. IV. ⁇ -rf.-.-* ⁇
- This invention contemplates fusing the gene enclosing the desired polypeptide (gene 1 ) to a second gene (gene 2) such that a fusion protein is generated during transcription.
- Gene 2 is typically a coat protein gene of a phage, and preferably it is the phage M13 gene III coat protein, or a fragment thereof. Fusion of genes 1 and 2 may be accomplished by inserting gene 2 into a particular site on a plasmid that contains gene 1 , or by inserting gene 1 into a particular site on a plasmid that contains gene 2.
- Insertion of a gene into a plasmid requires that the plasmid be cut at the precise location that the gene is to be inserted. Thus, there must be a restriction endonuclease site at this location (preferably a unique site such that the plasmid will only be cut at a single location during restriction endonuclease digestion).
- the plasmid is digested, phosphafased, and purified as described above.
- the gene is then inserted into this linearized plasmid by ligating the two DNAs together. Ligation can be accomplished if the ends of the plasmid are compatible with the ends of the gene to be inserted.
- the DNAs can be ligated together directly using a ligase such as bacteriophage T4 DNA ligase and incubating the mixture at 16'C for 14 hours in the presence of ATP and ligase buffer as described in section 1.68 of Sambrook et al., sucia. If the ends are not compatible, they must first be made blunt by using the Klenow fragment of DNA polymerase I or bacteriophage T4 DNA polymerase, both of which require the four deoxyribonucleotide triphosphates to fill-in overhanging single-stranded ends of the digested DNA.
- a ligase such as bacteriophage T4 DNA ligase
- the ends may be blunted using a nuclease such as nuclease S1 or mung-bean nuclease, both of which function by cutting back the overhanging single strands of DNA.
- the DNA is then religated using a ligase as described above.
- oligonucieotide linkers may be used. The linkers serve as a bridge to connect the plasmid to the gene to be inserted. These linkers can be made synthetically as double stranded or single stranded DNA using standard methods.
- the linkers have one end that is compatible with the ends of the gene to be inserted; the linkers are first ligated to this gene using ligation methods described above.
- the other end of the linkers is designed to be compatible with the plasmid for ligation.
- care must be taken to not destroy the reading frame of the gene to be inserted or the reading frame of the gene contained on the plasmid.
- it may be necessary to design the linkers such that they code for part of an amino acid, or such that they code for one or more amino acids.
- termination codons are UAG( amber), UAA (ocher) and UGA (opel). (Microbiology, Davis et al. Harper & Row, New York, 1980, pages 237, 245-47 and 274).
- the termination codon expressed in a wild type host cell results in the synthesis of the gene 1 protein product without the gene 2 protein attached.
- growth in a suppressor host cell results in the synthesis of detectable quantities of fused protein.
- Such suppressor host cells contain a tRNA modified to insert an amino acid in the termination codon position of the mRNA thereby resulting in production of detectible amounts of the fusion protein.
- suppressor host cells are well known and described, such as E.coli suppressor strain (Bullock et al., BioTechniques 5, 376-379 [1987]). Any acceptable method may be used to place such a termination codon into the mRNA encoding the fusion polypeptide.
- the suppressible codon may be inserted between the first gene encoding a polypeptide, and a second gene encoding at least a portion of a phage coat protein.
- the suppressible termination codon may be inserted adjacent to the fusion site by replacing the last amino acid triplet in the polypeptide or the first amino acid in the phage coat protein.
- the polypeptide When the phagemid is grown in a non-suppressor host cell, the polypeptide is synthesized substantially without fusion to the phage coat protein due to termination at the inserted suppressible triplet encoding UAG, UAA, or UGA. In the non-suppressor cell the polypeptide is synthesized and secreted from the host cell due to the absence of the fused phage coat protein which otherwise anchored it to the host cell. V. Alterationfmutatlon ⁇ of Gene 1 at Selected Positions
- Gene 1 encoding the desired polypeptide, may be altered at one or more selected codons.
- An alteration is defined as a substitution, deletion, or insertion of one or more codons in the gene encoding the polypeptide that results in a change in the amino acid sequence of the polypeptide as compared with the unaltered or native sequence of the same polypeptide.
- the alterations will be by substitution of at least one amino acid with any other amino acid in one or more regions of the molecule.
- the alterations may be produced be a variety of methods known in the art. These methods include but are not limited to oligonucieotide-mediated mutagenesis and cassette mutagenesis.
- Oligonucleotide -mediated mutagenesis is preferred method for preparing substitution, deletion, and insertion variants of gene 1. This technique is well known in the art as described by Zoller et al. Nucleic Acids Res. j£: 6487-6504 [1987]. Briefly, gene 1 is altered by hybridizing an oligonucleotide encoding the desired mutation to a DNA template, where the template is the single-stranded form of the plasmid containing the unaltered or native DNA sequence of gene 1. After hybridization, a DNA polymerase is used to synthesize an entire second complementary strand of the template will thus incorporate the oligonucleotide primer, and will code for the selected alteration in gene 1.
- oligonucleotides of at least 25 nucleotides in length are used.
- An optimal oligonucleotide will have 12 to 15 nucleotides that are completely complementary to the template on either side of the nudeotide(s) coding for the mutation. This ensures that the oligonucleotide will hybridize properly to the single-stranded DNA template molecule.
- the oligonucleotides are readily synthesized using techniques known in the art such as that described by Crea ef al. Proc. Natl. Acad. Sci. USA.75: 5765 [1978].
- the DNA template can only be generated by those vectors that are either derived from bacteriophage M13 vectors (the commercially available M13mp18 and M13mp19 vectors are suitable), or those vectors that contain a single-stranded phage origin of replication as described by Viera etal. Meth. E ⁇ zvmoL 153: 3 [1987].
- the DNA that is to be mutated must be inserted into one of these vectors in order to generate single- stranded template. Production of the single-stranded template is described in sections 4.214.41 of Sambrook etal., supra.
- the oligonucleotide is hybridized to the single stranded template under suitable hybridization conditions.
- a DNA polymerizing enzyme usually the Klenow fragment of DNA polymerase I, is then added to synthesize the complementary strand of the template using the oligonucleotide as a primer for synthesis.
- a heteroduplex molecule is thus formed such that one strand of DNA encodes the mutated form of gene 1 , and the other strand (the original template) encodes the native, unaltered sequence of gene 1.
- This heteroduplex molecule is then transformed into a suitable host cell, usually a prokaryote such as £ Coli JM101. After growing the cells, they are plated onto agarose plates and screened using the oligonucleotide primer radiolabelled with 32-Phosphate to identify the bacterial colonies that contain the mutated DNA.
- the method described immediately above may be modified such that a homoduptex molecule is created wherein both strands of the plasmid contain the mutation(s).
- the modifications are as follows:
- the single- stranded oligonucleotide is annealed to the single-stranded template as described above.
- a mixture of three deoxyribonucleotides, deoxyriboadenosine (dATP), deoxyriboguanosine (dGTP), and deoxyribothymidine (dTTP) is combined with a modified thio-deoxyribocytosine called dCTP-(aS) (which can be obtained from Amersham). This mixture is added to the template-oligonucleotide complex.
- a strand of DNA identical to the template except for the mutated bases is generated.
- this new strand of DNA will contain dCTP-(aS) instead of dCTP, which serves to protect it from restriction endonuclease digestion.
- the template strand can be digested with Exolll nuclease or another appropriate nuclease past the region that contains the site(s) to be mutagenized. The reaction is then stopped to leave a molecule that is only partially single-stranded.
- a complete double-stranded DNA homodupiex is then formed using DNA polymerase in the presence of all four deoxyribonucleotide triphosphates, ATP, and DNA ligase.
- This homodupiex molecule can then be transformed into a suitable host cell such as £ coli JM101 , as described above.
- Mutants with more than one amino acid to be substituted may be generated in one of several ways. If the amino acids are located close together in the polypeptide chain, they may be mutated simultaneously using one oligonucleotide that codes for all of the desired amino acid substitutions. If, however, the amino acids are located some distance from each other (separated by more than about ten amino acids), it is more difficult to generate a single oligonucleotide that encodes all of the desired changes. Instead, one of two alternative methods may be employed.
- a separate oligonucleotide is generated for each amino acid to be substituted.
- the oligonucleotides are then annealed to the single-stranded template DNA simultaneously, and the second strand of DNA that is synthesized from the template will encode all of the desired amino acid substitutions.
- the alternative method involves two or more rounds of mutagenesis to produce the desired mutant.
- the first round is as described for the single mutants: wild-type DNA is used for the template, an oligonucleotide encoding the first desired amino acid substitution(s) is annealed to this template, and the heteroduplex DNA molecule is then generated.
- the second round of mutagenesis utilizes the mutated DNA produced in the first round of mutagenesis as the template.
- this template already contains one or more mutations.
- the oligonucleotide encoding the additional desired amino acid substitution(s) is then annealed to this template, and the resulting strand of DNA now encodes mutations from both the first and second rounds of mutagenesis.
- This resultant DNA can be used as a template in a third round of mutagenesis, and so on.
- This method is also a preferred method for preparing substitution, deletion, and insertion variants of gene l.
- the method is based on that described by Wells ef al. Gene.34:315 [1985]..
- the starting material is the plasmid (or other vector) comprising gene 1 , the gene to be mutated.
- the codon(s) in gene 1 to be mutated are identified. There must be a unique restriction endonuclease site on each side of the identified mutation site(s). If no such restriction sites exist, they may be generated using the above-described oligonucleotide-mediated mutagenesis method to introduce them at appropriate locations in gene 1.
- the plasmid is cut at these sites to linearize it.
- a double-stranded oligonucleotide encoding the sequence of the DNA between the restriction sites but containing the desired mufation(s) is synthesized using standard procedures. The two strands are synthesized separately and then hybridized together using standard techniques.
- This double-stranded oligonucleotide is referred to as the cassette.
- This cassette is designed to have 3' and 5' ends that are compatible with t e ends of the linearized plasmid, such that it can be directly ligated to the plasmid.
- This plasmid now contains the mufated DNA sequence of gene 1.
- mis invention contemplates production of variants of a desired protein containing one or more subunits.
- Each subunit is typically encoded by separate gene.
- Each gene encoding each subunit can be obtained by methods known in the art (see, for example, Section II). In some instances, it may be necessary to obtain the gene encoding the various subunits using separate techniques selected from any of the methods described in Section II.
- all subunits can be regulated by the same promoter, typically located 5' to the DNA encoding the subunits, or each may be regulated by separate promoter suitably oriented in the vector so that each promoter is operabfy linked to the DNA it is intended to regulate . Selection of promoters is carried out as described in Section III above.
- Figure 10 In constructing a replicable expression vector containing DNA encoding the protein of interest having multiple subunits, the reader is referred to Figure 10 where, by way of illustration, a vector is diagrammed showing DNA encoding each subunit of an antibody fragment.
- a vector is diagrammed showing DNA encoding each subunit of an antibody fragment.
- This figure shows that generally, one of the subunits of the protein of interest will be fused to a phage coat protein such as M13 gene III. This gene fusion generally will contain its own signal sequence. A separate gene encodes the other subunit or subunits, and it is apparent that each subunit generally has its own signal sequence.
- Figure 10 also shows that a single promoter can regulate the expression of both subunits. Alternatively, each subunit may be independently regulated by a different promoter.
- the protein of interest subunit-phage coat protein fusion construct can be made as described in Section IV above.
- DNA encoding each subunit in the vector may mutated in one or more positions in each subunit
- preferred sites of mutagenesis correspond to codons encoding amino acid residues located in the complemenfarity-determining regions (CDR) of either the light chain, the heavy chain, or both chains.
- CDRs are commonly referred to as the hypervariable regions.
- Target proteins such as receptors
- glycoprotein hormone receptors may be prepared by the technique described by McFarland etal., Science 245:494499 [1989], nonglycosylated forms expressed in £ co// are described by Fuh et al. J. Biol. Chem 265:3111-3115 [1990]
- Other receptors can be prepared by standard methods.
- the purified target protein may be attached to a suitable matrix such as agarose beads, acrylamide beads, glass beads, cellulose, various acrylic copolymers, hydroxylalkyi methacrylate gels, polyacrylic and polymethacryiic copolymers, nylon, neutral and ionic carriers, and the like. Attachment of the target protein to the matrix may be accomplished by methods described in Methods in Enzvmologv .44 [1976], or by other means known in the art.
- the immobilized target is contacted with the library of phagemid particles under conditions suitable for binding of at least a portion of the phagemid particles with the immobilized target.
- the conditions including pH, ionic strength, temperature and the like will mimic physiological conditions.
- Binders Bound phagemid particles having high affinity for the immobilized target are separated from those having a low affinity (and thus do not bind to the target) by washing. Binders may be dissociated from the immobilized target by a variety of methods. These methods include competitive dissociation using the wild-type ligand, altering pH and/or ionic strength, and methods known in the art.
- Suitable host cells are infected with the binders and helper phage, and the host cells are cultured under conditions suitable for amplification of the phagemid particles.
- the phagemid particles are then collected and the selection process is repeated one or more times until binders having the desired affinity for the target molecule are selected.
- the library of phagemid particles may be sequentially contacted with more than one immobilized target to improve selectivity for a particular target. For example, it is often the case that a ligand such as hGH has more than one natural receptor. In the case of hGH, both the growth hormone receptor and the prolactin receptor bind the hGH ligand.
- hGH selectivity of hGH for the growth hormone receptor over the prolactin receptor. This can be achieved by first contacting the library of phagemid particles with immobilized prolactin receptor, eluting those with a low affinity (i.e. lower than wild type hGH) for the prolactin receptor and then contacting the low affinity prolactin 'binders * or non-binders with the immobilized growth hormone receptor, and selecting for high affinity growth hormone receptor binders. In this case an hGH mutant having a lower affinity for the prolactin receptor would have therapeutic utility even if the affinity for the growth hormone receptor were somewhat lower than that of wild type hGH. This same strategy may be employed to improve selectivity of a particular hormone or protein for its primary function receptor over its clearance receptor.
- an improved substrate amino acid sequence can be obtained. These may be useful for making better 'cut sites' for protein linkers, or for better protease substrates/inhibitors.
- an immobiiizabie molecule e.g. hGH-receptor, biotin-avidin, or one capable of covalent linkage with a matrix
- the linker will preferably be from 3 to 10 amino acids in length and will act as a substrate for a protease.
- a phagemid will be constructed as described above where the DNA encoding the linker region is randomly mutated to produce a randomized library of phagemid particles with different amino acid sequences at the linking site.
- the library cf phagemid particles are then immobilized on a matrix and exposed to a desired protease.
- Phagemid particles having preferred or better substrate amino add sequences in the liner region for the desired protease will be eluted, first producing an enriched pool of phagemid partides encoding preferred linkers. These phagemid partides are then cyded several more times to produce an enriched pool of particles encoding consense sequence(s) (see examples XIII and XIV).
- Gi-owthHoiroreVartai-teandMel- ⁇ The cloned gene for hGH has been expressed in a secreted form in Eschericha cola (Chang, C. N>, et al.,
- the present invention describes novel hGH variants produced using the phagemid selection methods. Human growth hormone variants containing substitutions at positions 10, 14, 18, 21 , 167, 171, 172, 174, 175, 176, 178 and 179 have been described. Those having higher binding affinities are described in Tables VII, XIII and XIV. The amino acid nomenclature for describing the variants is shown below. Growth hormone variants may be administered and formulated in the same manner as regular growth hormone. The growth hormone variants of the present invention may be expressed in any recombinant system which is capable of expressing native or met hGH.
- Therapeutic formulations of hGH for therapeutic administration are prepared for storage by mixing hGH having the desired degree of purity with optional physiologically acceptable carriers, excipients, or stabilizers (Remington's Pharmaceutical Sdences. 16th edition, Osol, A., Ed., (1980)., in the form of lyophilized cake or aqueous solutions.
- Acceptable carriers, excipients or stabilizers are nontoxic to redpients at the dosages and concentrations employed, and indude buffers such as phosphate, citrate, and other organic adds; antioxidants including ascorbic acid; low molecular weight (less than about 10 residues) poiypeptides; proteins, such as serum albumin, gelatin, or immunoglobulins; hydrophilic polymers such as pdyvinytpyrrolidone; amino adds such as glydne, glufamine, asparagine, arginine, or iysine; monosaccharides, disaccharides, and other carbohydrates induding glucose, mannose, or dextrins; chelating agents such as EDTA; divalent metal ions such as zinc, cobalt or copper; sugar alcohols such as marmitol or sorbitol; salt-forming counterions such as sodium; and/or nonionic surfactants such as Tween, Pluronics or polyethylene glycol
- Formulations of the present invention may additionally contain a pharmaceutically acceptable buffer, amino add, bulking agent and/or non-ionic surfactant These include, for example, buffers, chelating agents, antioxidants, preservatives, cosolvents, and the like; specific examples of these could indude, bimethylamaine salts (Tris buffer”), and disodiu edetate.
- the phagemids of the present invention may be used to produce quantities of the hGH variants free of the phage protein.
- pS0643 and derivatives can simply be grown in a non- suppressor strain such as 16C9. In this case, the amber codon (TAG) leads to termination of translation, which yields free hormone, without the need for an independent DNA construction.
- the hGH variant is secreted from the host and may be isolated from the culture medium.
- One or more of the eight hGH amino adds F10, M14, H18, H21, R167, D171,T175 and 1179 may bereped by any amino add other than the one found in that position in naturally occurring hGH as indicated. Therefore, 1 , 2, 3, 4, 5, 6,7, or all 8 of the indicated amino adds, F10, M14, H18, H21, R167, D171, T175 and 1179, maybe replaced by any of the other 19 amino acids out of the 20 amino acids listed below. In apreferred embodiment all eight listed amino acids are replaced by another amino acid. The most preferred eight amino acids to be substituted are indicated in Table XIV in Example XII. Airtno add nomenclature.
- phGH-M13glll The plasmid phGH-M13glll (Fig. 1), was constructed from M13K07 7 and the hGH producing plasmid, pB0473 (Cunningham, B. C, etal. , Science.243:1330-1336, [1989]).
- a synthetic oligonucleotide 5'-AGC- TGT-GGC-TTC-GGG-CCC-TTA-GCA-TTT-AAT-GCG-GTA-3' was used to introduce a unique Apal restriction site (underlined) into pB0473 after the final Phe191 codon of hGH.
- the oligonudeotide 5'-TTC- ACA-AAC-GAA-GGG-CCC-CTA-ATT-AAA-GCC-AGA-3' was used to introduce a unique Apa ⁇ restriction site (underlined), and a Glu197-to-amber stop codon (bold lettering) into M13K07 gene III.
- the oligonudeotide 5'- CAA-TAA-TAA-CGG-GCT-AGC-CAA-AAG-AAC-TGG-3' introduces a unique Nhe ⁇ site (underlined) after the 3' end of the gene III coding sequence.
- the resulting 650 base pair (bp) Apa ⁇ -Nhe ⁇ fragment from the doubly mutated M13K07 gene III was cloned into the large Apa ⁇ -Nne ⁇ fragment of pB0473 to create the plasmid, pS0132.
- This fuses the carboxyl terminus of hGH (Phe191) to the Pro198 residue of the gene III protein with the insertion of a glydne residue encoded from the Apal site and places the fusion protein under control of the £ coli alkaline phosphatase (pft ⁇ A) promoter and stll secretion signal sequence (Chang, C. N., etal. , Q ⁇ , 55:189-196, [1987]).
- the R64A variant hGH phagemid was constructed as follows: the Nsil-Bglll mutated fragment of hGH (Cu ⁇ ninghamef at supra ) encoding the Arg64 to Ala substitution (R64A) (Cunningham, B. C, Wells, J. A.. Sde ⁇ ce.244:1081-1085. [1989]) was cloned between the corresponding restriction sites in the phGH-M13glll plasmid (Rg. 1) to replace the wild-type hGH sequence.
- the R64A hGH phagemid partides were propagated and titered as described below for the wild-type hGH-phagemid.
- Plasmids were transformed into a male strain of £ coli (JM 101) and selected on carbenidllin plates. A single transformant was grown in 2 ml 2YT medium for 4 h at 37'C and infected with 50 ⁇ l of M13K07 helper phage. The infected culture was diluted into 30 ml 2YT, grown overnight and phagemid partides were harvested by predpitation with polyethylene glycol (Vierra, J., Messing, J..Methods in Enzymology.153:3-11, [1987]). Typical phagemid ought ranged from 2 to 5 x 10 11 cfu/ml.
- hGH or hGH-phagemid partides were serially diluted from 2.0 - 0.002 nM in buffer A (50 mM Tris (pH 7.5), 50 mM NaCl, 2 mM EDTA, 5 mg/ml bovine serum albumin, and 0.05% Tween 20). After 2 hours at room temperature (rt), the plates were washed well and the indicated Mab (Cun ⁇ inghamef a/, supra ) was added at 1 ⁇ g/ml in buffer A for 2 hours at rt. Following washing, horseradish peroxidase conjugated goat anti-mouse IgG antibody was bound at rt for 1 hour. After a final wash, the peroxidase activity was assayed with the substrate, ⁇ -phe ⁇ yienediamine. EXAMPLE 111
- Oxirane polyacrylamide beads (Sigma) were conjugated to the purified extracellular domain of the hGH receptor (hGHbp) (Fuh, G., etal., J. Biol. Chem.. 265:3111-3115 [1990]) containing an extra cysteine residue introduced by site-directed mutagenesis at position 237 that does not affect binding of hGH (J. Wells, unpublished).
- the hGHbp was conjugated as recommended by the supplier to a level of 1.7 pmol hGHbp/mg dry oxirane bead, as measured by binding of [ 125 l] hGH to the resin. Subsequently, any unreacted oxirane groups were blocked with BSA and Tris. As a control for non-spedfic binding of phagemid partides, BSA was similarly coupled to the beads. Buffer for adsorption and washing contained 10 mM Tris-HCI (pH 7.5), 1 mM EDTA, 50 mM NaCl, 1 mg/ml BSA, and 0.02% Tween 20.
- Elution buffers contained wash buffer plus 200 nM hGH or 0.2 M glydne (pH 2.1).
- Parental phage M13K07 was mixed with hGH phagemid particles at a ratio of nearly 3000:1 (original mixture) and tumbled for 8-12 h with a 5 ⁇ l aliquot (0.2 mg of acrylamide beads) of either absorbent in 50 ⁇ l volume at room temperature.
- the beads were pelleted by centrifugation and the supernate carefully removed. The beads were resuspended in 200 ⁇ l wash buffer and tumbled at room temperature for 4 hours (wash 1).
- wash 2 After a second wash (wash 2), the beads were eluted twice with 200 nM hGH for 6-10 hours each (eluate 1 , eluate 2). The final elution was with a glydne buffer (pH 2.1) for 4 hours to remove remaining hGH phagemid partides (eluate 3). Each fraction was diluted appropriately in 2YT media, mixed with fresh JM101, incubated at 37'C for 5 minutes, and plated with 3 ml of 2YT soft agar on LB or LB carbenicillin plates.
- the gene III protein is composed of 410 residues divided into two domains that are separated by a flexible linker sequence (Armstrong, J., etal., FEBS Lett..135:167-172, [1981]).
- the amino-terminal domain is required for attachment to the pili of £ coli, while the carboxyl-terminal domain is imbedded in the phage coat and required for proper phage assembly (Crissman, J. W., Smith, G. P., Virology. 132:445455, [1984]).
- the signal sequence and amino-terminal domain of gene III was replaced with the stll signal and entire hGH gene (Chang et al.
- hGH-gene III fusion was placed under control of the lac promoter/operator in a plasmid (phGH-M13glll; Fig. 1) containing the pBR322 ⁇ -lactamase gene and Col E1 replication origin, and the phage f 1 intergenic region.
- the vector can be easily maintained as a small plasmid vector by selection on carbeni iiin, which avoids relying on a functional gene III fusion for propagation.
- the plasmid can be efficiently packaged into virions (called phagemid partides) by infection with helper phage such as M13K07 (Viera etal.. supra ) which avoids problems of phage assembly.
- helper phage such as M13K07 (Viera etal.. supra ) which avoids problems of phage assembly.
- Phagemid infectivity titers based upon transduction to carbenidiiin resistance in this system varied from 2-5 x 10 1 colony forming units (cfuVml.
- the titer of the M13K07 helper phage in these phagemid stocks is ⁇ 10 1 ⁇ plaque forming units (pfu)/ml.
- the titer of fusion phage displaying the hGH gene III fusion is about 2 - 5 x 10 1 0/ml. This number is much greater than the titer of £ coli (-10 8 to 10 9 /ml) in the culture from which they are derived. Thus, on average every £ coli cell produces 10-100 copies of phage decorated with an hGH gene III fusion protein.
- Beads Provides an Enrichment for hGH-phage over M13K07 Phage*
- ⁇ E ⁇ richments are calculated by dividing the cfu/pfu ratio after each step by cfu/pfu ratio in the original mixture.
- a fusion phagemid was constructed with an hGH mutant in which Arg64 was substituted with Ala (R64A).
- the R64A variant hormone is about 20- fold reduced in receptor binding affinity compared to hGH (Kd values of 7.1 nM and 0.34 nM, respectively
- the titers of the R64A hGH-gene III fusion phagemid were comparable to those of wild-type hGH phagemid. After one round of binding and elution (Table III) the wild-type hGH phagemid was enriched from a mixture of the two phagemids plus M13K07 by 8-fold relative to the phagemid R64A, and ⁇ 10 4 relative to M13K07 helper phage.
- hGHbp beads as described in Table II and the Materials and Methods After each step, plasmid DNA was isolated(Birnboim, H. C, Doty, J. , Nucleic Adds Res..7:1513-1523, [1979]) from carbenidiiin resistant colonies and analyzed by restriction analysis to determine if it contained the wild-type hGH or the R64A hGH gene ill fusion. TThe enrichment for wild-type hGH phagemid over R64A mutant was calculated from the ratio of hGH phagemid present after each step to that present in the original mixture (8/20), divided by the corresponding ratio for
- a mutant of the hGH-gene III fusion protein was constructed using the method of KunkeL.ef al. Meth. Enzymol.154, 367-382 [1987].
- Template DNA was prepared by growing the plasmid pS0132 (containing the natural hGH gene fused to the carboxy-terminal half of M13 gene III, under control of the alkaline phosphatase promoter) in CJ236 cells with M13-K07 phage added as helper.
- Single-stranded, uradl-containing DNA was prepared for mutagenesis to introduce (1 ) a mutation in hGH which would greatly reduce binding to the hGH binding protein (hGHbp); and (2) a unique restriction site (Kpnl) which could be used for assaying for ⁇ and selecting against - parental background phage.
- Oligonudeotide-directed mutagenesis was carried out using T7 DNA polymerase and the following oligodeoxy-nucieotide:
- This oligo introduces the Kpnl site as shown, along with mutations (R178G, I179T) in hGH. These mutations are predicted to reduce binding of hGH to hGHbp by more than 30-fold.
- Clones from the mutagenesis were screened by Kpnl digestion and confirmed by dideoxy DNA sequendng. The resulting construct, to be used as a template for random mutagenesis, was designated pH0415.
- Codons 172, 174, 176, 178 were targeted for random mutagenesis in hGH, again using the method of
- NPS random codons
- Propagation of the Initial library The mutagenesis products were extracted twice with phenolxhloroform (50:50) and ethanol predpitated with an excess of carrier tRNA to avoid adding salt that would confound the subsequent electroporation step.
- dsDNA double-stranded DNA
- phage pool ⁇ 1 The supernatant was spun again to remove any remaining cells, and the phage, designated phage pool ⁇ 1 , were PEG-predpitated and resuspended in 1 mL STE buffer (10 mM Tris, pH 7.6, 1 mM EDTA, 50 mM NaCl). Phage titers were measured as colony-forming units (CFU) for the recombinant phagemid containing hGH-g3p gene III fusion (hGH-g 3 ) plasmid, and plaque-forming units (PFU) for the M13-K07 helper phage.
- CFU colony-forming units
- BINDING An aliquot of phage pool ⁇ j>1 (6 x 10 9 CFU, 6 x 10 7 PFU) was diluted 4.5-fold in buffer A (Phosphate-buffered saline, 0.5% BSA, 0.05% Twee ⁇ -20, 0.01% thimerosal) and mixed with a 5 ⁇ L suspension of oxirane-polyacrylamide beads coupled to the hGHbp containing a Ser237 Cys mutation (350 fmols) in a 1.5 mL silated polypropylene tube.
- buffer A Phosphate-buffered saline, 0.5% BSA, 0.05% Twee ⁇ -20, 0.01% thimerosal
- an equivalent aliquot of phage were mixed in a separate tube with beads that had been coated with BSA only.
- the phage were allowed to bind to the beads by incubating 3 hours at room temperature (23°C) with slow rotation (approximately 7 RPM). Sub
- hGH ELUTION Phage/phagemid binding weakly to the beads were removed by stepwise elution with hGH. In the first step, the beads were rotated with buffer A containing 2 nM hGH. After 17 hours , the beads were pelleted and resuspended in buffer A containing 20 nM hGH and rotated for 3 hours, then pelleted. In the final hGH wash, the beads were suspended in buffer A containing 200 nM hGH and rotated for 3 hours then pelleted.
- GLYCINE ELUTION To remove the tightest-binding phagemid (i.e. those still bound after the hGH washes), beads were suspended in Glydne buffer (1 M.Gtydne, pH 2.0 with HCl), rotated 2 hours and pelleted. The supernatant (fraction "G"; 200 ⁇ L) was neutralized by adding 30 ⁇ L of 1 M Tris base. Fraction G eluted from the hGHbp-beads (1 x 10 6 CFU, 5 x 10 4 PFU) was not substantially enriched for phagemid over K07 helper phage.
- PROPAGATION An aliquot (4.3 x 10 5 CFU) of fraction G eluted from the hGHbp-beads was used to Infect log-phase WJM101 cells. Transductions were carried out by mixing 100 ⁇ L fraction G with 1 mL WJM101 cells, incubating 20 min. at 37°C, then adding K07 (multiplicity of infection- *** 1000). Cultures (25 mL 2YT plus carbenidiiin) were grown as described above and the second pool of phage (Library 1G, for first glydne elution) were prepared as described above.
- Phage from library 1 G (Fig.3) were selected for binding to hGHbp beads as described above. Fraction G eluted from hGHbp beads contained 30 times as many CFU's as fraction G eluted from BSA-beads in this selection. Again, an aliquot of fraction G was propagated in WJM101 cells to yield library 1G 2 (indicating that this library had been twice selected by glydne elution). Double-stranded DNA (pLIB 1G 2 ) was also prepared from this culture.
- Kpnl assay and restriction-selection of dsDNA To reduce the level of background (Kpnl *1* ) template, an aliquot (about 0.5 ⁇ g) of pLIB 1 G 2 was digested with Kpnl and electroporated into WJM101 cells. These cells were grown in the presence of K07 (multiplicity of infection ⁇ 100) as described for the initial library, and a new phage pool, pLIB 3, was prepared (Fig. 3).
- phage Library 2 (Fig.3). Successive rounds of selection
- Phagemid binding, elution, and propagation were carried out in successive rounds for phagemid derived from both pLIB 2 and pLIB 3 (Fig.3) as described above, except that (1) an excess (10-fold over CFU) of purified K07 phage (not displaying hGH) was added in the bead-binding cocktail, and (2) the hGH stepwise elutions were replaced with brief washings of buffer A alone. Also, in some cases, XL1 -Blue cells were used for phagemid propagation.
- hGH codon 172 174 176 178 5' -AAG GTC TCC ACA TAC CTG AGG ATC-3'
- Residue 172 in these clones is Lys as in wild- type.
- the codon selected for 172 is also identical to wild-type hGH. This is not surprising since AAG is the only lysine-codon possible from a degenerate "NNS" codon set.
- Residue 178-Arg is also the same as wild-type, but here, the codon selected from the library was AAG instead of CGC as is found in wild-type hGH, even though the latter codon is also possible using the "N NS" codon set. Multiplicity of K07 Infection
- the multiplidty of infection of K07 infection is an important parameter in the propagation of recombinant phagemids.
- the K07 multiplidty of infection must be high enough to insure that virtually all cells transformed or transfected with phagemid are able to package new phagemid partides.
- the concentration of wild-type gene III in each cell should be kept high to reduce the possibility of multiple hGH-gene III fusion molecules being displayed on each phagemid moussee, thereby redudng chelate effects in binding.
- the K07 multiplidty of infection is too high, the packaging of K07 will compete with that of recombinant phagemid. We find that acceptable phagemid yields, with only 1 -10% background K07 phage, are obtained when the K07 multiplidty of infection is 100.
- Phage pools are labelled as shown (Rg.3).
- the multiplidty of infection (moi) refers to the multiplidty of K07 infection (PFU/cells) in the propagation of phagemid.
- the enrichment of CFU over PFU is shown in those cases where purified K07 was added in the binding step.
- the ratio of CFU eluting from hGHbp-beads over CFU eluting from BSA-beads is shown.
- the fraction of Kpnl-containi ⁇ g template (i.e., pH0415) remaining in the pool was determined by digesting dsDNA with Kpnl plus EcoRl, running the products on a 1 % agarose gel, and laser- scanning a negative of the ethidium bromide-stained DNA. Receotor-blndinq affinity of the hormone hGH(E174S. F176Y) The fact that a single done was isolated from two different pathways of selection (Rg.3) suggested that the double mutant (E174S.F176Y) binds strongly to hGHbp.
- this mutant of hGH by site-directed mutagenesis, using a plasmid (pB0720) which contains the wild-type hGH gene as template and the following oligonucleotide which changes codons 174 and 176 : hGH codon: 172 174 176 178 Lys Ser Tyr Arg 5'- ATG GAC AAG GT.1£G ACA T C CTG CGC ATC GTG -3'
- Human growth hormone variants were produced by the method of the present invention using the phagemid described in figure 9.
- Plasmid pS0643 was constructed by oligonudeotide-directed mutagenesis (Kunkel et at, Methods
- pS0643 and derivatives can be grown in a amber- suppressor strain of E. coli. such as JM101 or XL1-Blue (Bullock et al., BioTechniques 5, 376-379 [1987]). Shown above is substitution of Glu at the amber codon which occurs in supE suppressor strains. Suppression with other amino acids is also possible in various available strains of E. coli well known and publically available.
- pS0643 and derivatives can simply be grown in a non-suppressor strain such as 16C9.
- the amber codon (TAG) leads to termination of translation, which yields free hormone, without the need for an independent DNA construction.
- pS0643 was mufated with the oiigonudeotides (1) 5'-CGG- ACT-GGG-CAG-ATA-TTC-AAG-CAG-ACC-3'. which destroys the unique fipjj] site of pS0643; (2) 5'-CTC- AAG-AAC-TAC-GGG-TTA-CCC-TGA-CTG-CTT-CAG-GAA-GG-3'.
- the BstEII - fifllll segment is cut out of pH0509 and replaced with a DNA cassette, mutated at the codons of interest
- Other restriction sites for cassette mutagenesis at other locations in hGH have also been introduced into the hor one-phage vector.
- CassettemutaoenesiswithInhelix4ofhGH Codons 172, 174, 176 and 178 of hGH were targeted for random mutagenesis because they all lie on or near the surface of hGH and contribute significantly to receptor-binding (Cunningham and Wells. Science 244. 1081-1085 [1989]); they all lie within a well-defined structure, occupying 2 turns' on the same side of helix 4; and they are each substituted by at least one amino add among known evolutionary variants of hGH.
- TAG amber
- the vector was prepared by digesting pH0509 with BstEII followed by Bglll. The products were run on a 1 % agarose gel and the large fragment exdsed, phenol-extracted, and ethanol predpitated. This fragment was treated with calf intestinal phosphatase (Boehringer), then phenolxhloroform extracted, ethanol predpitated, and resuspended for ligation with the mutagenic cassette.
- reaction products were again digested with BstEII. then phenol -chloroform extracted, ethanol precipitated and resuspended in water.
- a BstEjll recognition site (GGTNACC) is created within cassettes which contain a Q. at position 3 of codon 172 and an A££ (Thr) codon at 174.
- dsDNA double-stranded DNA
- phage pool ⁇ H0529E the initial library of phage
- Phage titers were measured as colony-forming units (CFU) for the recombinant phagemid containing hGH-g3p. Approximately 4.5 x 10 13 CFU were obtained from the starting library. Degeneracy of the starting library
- Codon distribution (per 188 codons) of non-selected hormone phage. Clones were sequenced from the starting library (pH0529E). All codons were tabulated, induding those from dones which contained spurious mutations and/or frameshifts. * Note: the amber stop codon (TAG) is suppressed as Glu in XL1-Blue cells. Highlighted codons were over/under-represented by 50% or more.
- Non-selected dones with an open reading frame.
- the notation e.g.TWGS, denotes the hGH mutant 172T/174W/176G/178S.
- Amber (TAG) codons translated as Glu in XL1 -Blue cells are shown as ⁇ .
- hGHbp-beads * Immobilized hGHbp
- Bass et at, Proteins 8. 309-31 [1990] was prepared as described (Bass et at, Proteins 8. 309-31 [1990]), except that wild-type hGHbp (Fuh et al., J. Biol. Chem. 265, 3111-3115 [1990]) was used.
- hPRLbp-beads Immobilized hPRLbp
- hPRLbp-beads was prepared as above, using the 211 -residue extracellular domain of the prolactin receptor (Cunningham et at, Science 250.1709-1712 [1990]).
- Buffer A PBS, 0.5% BSA, 0.05% Tween 20, 0.01% ttiimerosal
- Buffer B 50 mM tris pH 7.5, 10 mM MgCfe 0.5% BSA, 0.05% Tween 20, 100 mM ZnCfe
- Buffer C PBS, 0.5% BSA, 0.05% Tween 20, 0.01% thimerosal. 10 mM EDTA) for selections using hPRLbp in the absence of zinc (+ EDTA).
- Binding selections were carried out according to each of the following paths: (1) binding to blank beads, (2) binding to hGHbp-beads, (3) binding to hPRLbp-beads (+ Zn 2+ ), (4) binding to hPRLbp-beads (+ EDTA), (5) pre-adsorbing twice with hGHbp beads then binding the non-adsorbed fraction to hPRLbp-beads
- BINDING An aliquot of hormone phage (typically 10 9 -10 t0 CFU) was mixed with an equal amount of non-hormone phage (pCAT), diluted into the appropriate buffer (A, B, or C), and mixed with a 10 mL suspension of hGHbp, hPRLbp or blank beads in a total volume of 200mL in a 1.5 L polypropylene tube. The phage were allowed to bind to the beads by incubating 1 hour at room temperature (23°C) with slow rotation (approximately 7 RPM). Subsequent steps were carried out with a constant volume of 200 ⁇ L and at room temperature.
- pCAT non-hormone phage
- WASHES The beads were spun 15 sec, and the supernatant was removed. To reduce the number of phage not spedfically bound, the beads were washed 5 times by resuspending briefly in the appropriate buffer, then pelleting.
- hGH ELUTION Phage binding weakly to the beads were removed by elution with hGH. The beads were rotated with the appropriate buffer containing 400 nMJiGH for 15-17 hours. The supernatant was saved as the 'hGH elution" and the beads. The beads were washed by resuspending briefly in buffer and pelleting. 4. GLYCINE ELUTION: To remove the tightest-binding phage (i.e. those still bound after the hGH wash), beads were suspended in Glydne buffer (Buffer A plus 0.2 J ⁇ Glydne, pH 2.0 with HCl), rotated 1 hour and pelleted. The supernatant ("Glydne elution"; 200 ⁇ L) was neutralized by adding 30 mL of 1 M Tris base and stored at 4° C.
- PROPAGATION Aliquots from the hGH elutions and from the Glydne elutions from each set of beads under each set of conditions were used to infect separate cultures of log-phase XL1 -Blue cells.
- Phage binding, elution, and propagation were carried out in successive rounds, according to the cyde described above.
- the phage amplified from the hGH elution from hGHbp-beads were again selected on hGHbp-beads and eluted with hGH, then used to infect a new culture of XL1-Blue cells.
- Three to five rounds of selection and propagation were carried out for each of the selection procedures described above.
- Mutants of hGH were prepared from osmoticaily shocked cells by ammonium sulfate precipitation as described for hGH (Olson et at, Nature 293, 408-411 [1981]), and protein concentrations were measured by laser densitomoetry of Coomassie-sfained SDS-polyacrylamide gel electrophoresis gels, using hGH as standard (Cunningham and Wells. Science 244. 1081-1085 [1989]). The binding affinity of each mutant was determined by displacement of 125 1 hGH as described (Spencer et al., J. Biol. Chem.263, 7862-7867 [1988] ; Fuh et al., J. Biol. Chem.265, 3111-3115 [1990]), using an anti- receptor monodonal antibody (Mab263).
- Binding assays may be carried out for mutants selected for hPRLbp-binding.
- the selected pool in which each mufant was found is indicated as 1 G (first glydne selection), 3G (third glycine selection), 3H (third hGH selection), 3 * (ttiird selection, not binding to hPRLbp, but binding to hGHbp).
- substitution of a particular amino add has essentially the same effect independent of 0 surrounding residues.
- substitution of F176Y in the background of 172R/174S reduces binding affinity by 2.0-fold (RSFR vs. RSYR).
- the binding affinity of the F176Y mutant (KAYR) is 2.9-fold weaker than the corresponding 176F mutant (KAFR; Cunningham and Wells, 1989).
- the binding constants determined for several selected mutants of hGH demonstrate non-additive effects of some amino add substitutions at residues 172, 174, 176, and 178.
- Example VIII Using the methods described in Example VIII, we targeted another region of hGH involved in binding to the hGHbp and/or hPRLbp, helix 1 residues 10, 14, 18, 21, for random mutagenesis in the phGHam-g3p vector (also known as pS0643; see Example VIII).
- phGHam-g3p the "amber" hGH-g3 construct
- Phage produced from both pS0132 S. Bass, R. Greene, J. A.
- Phagemid partides from phGHam-g3 reacted much more strongly with antibodies Medix 2, 1B5.G2, and 5B7.C10 than did phagemid particles from pS0132. in particular, binding of pS0132 particles was reduced by >2000-fokl for both Medix 2 and 5B7.C10 and reduced by >25-fold for 1B5.G2 compared to binding to Medix 1.
- binding of phGHam-g3 phage was weaker by only about 1.5-fold, 1.2-fold, and 2.3- fold for the Medix 2, 1B5.G2, and 5B7.C10 antibodies, respectively, compared with binding to MEDIX 1.
- This library was constructed by cassette mutagenesis that fully mutated four residues at a time (see Example VIII) which utilized a mutated version of phGHam-g3 into which unique Kpnl (at hGH codon 27)and Xho ⁇ (at hGH codon 6) restriction sites (underiined below) had been inserted by mutagenesis [ T. A. Kunkel, J. D. Roberts, R. A.
- the later oligo also introduced a +1 frameshift (italicized) to terminate translation from the starting vector and minimize wild-type background in the phagemid library. This strafing vector was designated pH0508B.
- the helix 1 library which mufated hGH residues 10, 14, 18, 21, was constructed by ligating to the large Xho ⁇ -Kpn ⁇ fragment of pH0508B a cassette made from the complementary oligonucleotides 5'-pTCG AGG CTC NNS GAC AAC GCG NNS CTG CGT GCT NNS CGT CTT NNS CAG CTG GCC TTT GAC ACG TAC-3" and 5'-pGT GTC AAA GGC CAG CTG SNN AAG ACG SNN AGC ACG CAG SNN CGC GTT GTC SNN GAG CC-3'.
- the Kpnl site was destroyed in the junction of the ligation product so that restriction enzyme digestion could be used for analysis of non-mutated background.
- the library contained at least 10 7 independent transformants so that if the library were absolutely random (10 6 different combinations of codons) we would have an average of about 10 copies of each possible mutated hGH gene. Restriction analysis using Kpnl indicated that at least 80% of helix 1 library constructs contained the inserted cassette.
- Binding enrichments of hGH-phage from the libraries was carried out using hGHbp immobilized on oxirane-potyacrylamide beads (Sigma Chemical Co.) as described (Example VIII).
- Four residues in helix 1 (F10, M14, H18, and H21) were similarly mufated and after 4 and 6 cycles a non-wild-type consensus developed (Table VIII).
- Position 10 on the hydrophobic face of helix 1 tended to be hydrophobic whereas positions 21 and 18 on the hydrophillic face tended were dominated by Asn; no obvious consensus was evident for position 14 (Table IX).
- the binding constants for these mutants of hGH to hGHbp was determined by expressing the free hormone variants in the non-suppressor E.
- Variants of hGH (randomly mutated at residues F10, M14, H18, H21) expressed on phagemid particles were selected by binding to hGHbp-beads and eluting with hGH (0.4 mM) buffer followed by glycine (0.2 M, pH 2) buffer (see Example VIII).
- Observed frequency is fraction of all clones sequenced with the indicated amino acid.
- the nominal frequency is calculated on the basis of NNS 32 codon degeneracy.
- the maximal enrichment factor varies from 11 to 32 depending upon the nominal frequency value for a given residue.
- Values of [Kd(Ala mut)/K(j(wt hGH)] for single alanine mutations were taken from B. C. Cunningham and J. A. Wells, Science 244, 1081 (1989); B. C. Cunningham, D. J. Henner, J. A. Wells, Science 247, 1461 (1990); B. C. Cunningham and J. A. Wells, Proc. Natl. Acad. Sci. USA 88, 3407 (1991).
- the helix 4b library was constructed in an attempt to further improve the helix 4 double mufant (E174S/F176Y) selected from the helix 4a library that we found bound tighter to the hGH receptor (see Example VIII). With the E174S/F176Y hGH mufant as the background sfarting hormone, residues were mutated that surrounded positions 174 and 176 on the hydrophilic face of helix 4 (R167, D171, T175 and 1179) . Construction of the helix 4b library bv cassette mutagenesis
- the binding constants for some of these mutants of hGH to hGHbp was determined by expressing the free hormone variants in the non-suppressor £ coli strain 16C9, purifying the protein, and assaying by competitive displacement of labelled wt-hGH from hGHbp (see Example VIII). As indicated, the binding affinities of several helix-4b mutants for hGHbp were tighter than that of wt-hGH Table XIII). Receptor-selectivity of hGH variants
- the E174S F176Y mutant binds 200-fold weaker to the hPRLbp than hGH.
- the E174T/F176Y/R178K and R167N/D171S/E174S/F176Y/I179T mutants each bind >500-fold weaker to the hPRLbp than hGH.
- Hormone-phagemid selection Identifies the Info ⁇ -natton-contentof particular residues
- the alanine- scanning information is useful for targeting side-chains that modulate binding, and the phage selection is appropriate for optimizing them and defining the flexibility of each site (and/or combinations of sites) for substitution.
- the combination of scanning mutationai methods [B. C. Cunningham, P. Jhurani, P. Ng, J. A. Wells, Science 243, 1330 (1989); B. C. Cunningham and J. A. Wells, Science 244, 1081 (1989)] and phage display is a powerful approach to designing receptoNigand interfaces and studying molecular evolution in vitro. Variations on Iterative enrichment of hormone-phaoemid libraries
- hormone phagemid enrichment can be carried out by one of several variations on the iterative enrichment approach : (1) random DNA libraries can be generated in each of two (or perhaps more) regions of the molecule by cassette or another mutagenesis method.
- a combined library can be created by ligation of restriction fragments from the two DNA libraries; (2) an hGH variant, optimized for binding by mutation in one region of the molecule, can be randomly mufated in a second region of the molecule as in the helix-4b library example; (3) two or more random libraries can be partially selected for improved binding by hormone-phagemid enrichment; after this "roughing-in" of the optimized binding site, the still-partially-diverse libraries can be recombined by ligation of restriction fragments to generate a single library, partially diverse in two or more regions of the molecules, which in turn can be further selected for optimized binding using hormone-phagemid enrichment.
- hGH helix 4b mutants (randomly mufated at residues 167, 171, 175, 179), each containing the E174S/F17 double mutant, by binding to hGHbp-beads and eluting with hGH (0.4 M) buffer followed by glydne (0.2 ⁇ f, pH 2) bu One mufant (+) contained the spurious mutation R178H.
- Plasmid pDH 188 confains the DNA encoding the Fab P° ⁇ - ⁇ l of a humanized IgG antibody, called 4D5, that recognizes the HER-2 receptor. This plasmid is contained in £ co ⁇ strain SR 101, and has been deposited with the ATCC in Rockville, MD.
- the plasmid was prepared as follows: the starting plasmid was pS0132, containing the alkaline phosphatase promoter as described above.
- the DNA encoding human growth hormone was exdsed and, after a series of manipulations to make the ends of the plasmid compatible for ligation, the DNA encoding 4D5 was inserted.
- the 4D5 DNA confains two genes. The first gene encodes the variable and consfant regions of the light chain, and contains at its 5' end the DNA encoding the st II signal sequence. The second gene contains four portions: first, at its 5' end is the DNA encoding the st II signal sequence.
- PEG polyethylene glycol
- electroporation Both polyethylene glycol (PEG) and electroporation were used to transform plasmids into SR101 cells.
- PEG competent cells were prepared and transformed according to the method of Chung and Miller (Nucleic Adds Res.16:3580 [1988]). Cells that were competent for electroporation were prepared, and subsequently transformed via electroporation according to the method of Zabarovsky and Winberg (Nucleic Acids Res.18:5912 [1990]). After pla ⁇ ' ng the cells in 1 ml of the SOC media (described in Sambrook etal., supra), they were grown for 1 hour at 37°C with shaking.
- the concentration of the cells was determined using light scattering at OD600- A titered K07 phage stock was added to achieve an multiplidty of infection (MOI) of 100, and the phage were allowed to adhere to the cells for 20 minutes at room temperature. This mixture was then diluted into 25 mis of 2YT broth (described in Sambrook ef al., supra) and incubated with shaking at 37°C overnight. The next day, cells were pelleted by centrifugation at 5000 x g for 10 minutes, the supernatant was collected, and the phage partides were predpitated with 0.5 M NaCl and 4% PEG (final concentration) at room temperature for 10 minutes.
- MOI multiplidty of infection
- Phage partides were pelleted by centrifugation at 10,000 x g for 10 minutes, resuspended in 1 ml of TEN (10 mM Tris, pH 7.6, 1 mM EDTA, and 150 mM NaCl), and stored at 4°C. Production of antigen coated plates.
- buffer A PBS, 0.5% BSA, and 0.05% Tween-20
- Elution of the phage from the plates was done at room temperature by one of two methods: 1) an initial overnight incubation of 0.025 mg/ml purified Mu4D5 antibody (murine) followed by a 30 minute incubation with 0.4 ml of the add elution buffer (0.2 M glydne, pH 2.1 , 0.5% BSA, and 0.05% Tween-20), or 2) an incubation with the acid elution buffer alone. Eluates were then neutralized with 1 M Tris base, and a 0.5 ml aliquot of TEN was added. These samples were then propagated, titered, and stored at 4°C. Phage propagation
- the affinity of h4D5 F a b fragments and F a b phage for the ECD antigen was determined using a competitive receptor binding RIA (Burt, D. R., Receptor Binding in Drug Research. O'Brien, R.A. (Ed.), pp.3- 29, Dekker, New York [1986]).
- the ECD antigen was labeled with 125 -k>dine using the sequential chloramine-T method (De Larco, J. E. etal., J. Cell.
- the labeled ECD-Fab or ECD-F aD phage complex was separated from the unbound labeled antigen by forming an aggregate complex induced by the addition of an anti-human IgG (Fitzgerald 40-GH23) and 6% PEG 8000.
- the complex was pelleted by centrifugation (15,000 x g for 20 minutes) and the amount of labeled ECD (in cpm) was determined by a gamma counter.
- the dissociation constant (Kd) was calculated by employing a modified version of the program LIGAND (Munson, P. and Rothbard, D., Ami. Biochem.107 * 220-239 [1980]) which utilizes Scatchard analysis (Scatchard, G.,A ⁇ .
- hGH-phagemid double-stranded DNA (dsDNA) from each of the one-helix variants was isolated and digested with the restriction enzymes EcoRl and BstX ⁇ . The large fragment from each helix-4b variant was then isolated and ligated with the small fragment from each helix-1 variant to yield the new two-helix variants shown in Table XIII. All of these variants also contained the mufations E174S/F176Y obtained in earlier hGH-phage binding selections (see Example X for details). Construction of selective combinatorial libraries of hGH
- hGH-phagemid double-stranded DNA from each of the one-helix library pools (selected for 0, 2, or 4 rounds) was isolated and digested with the restriction enzymes Acd and BstX ⁇ .
- the large fragment from each helix-1 variant pool was then isolated and ligated with the small fragment from each helix-4b variant pool to yield the three combinatorial libraries pH0707A (unselected helix 1 and helix 4b pools, as described in examples IX and X), pH0707B (twice-selected helix-1 pool with twice-selected helix-4b pool), and pH0707C (4-times selected helix-1 pool with 4-times selected helix-4b pool).
- the ligation products pH0707A-F were processed and electro-transformed into XL1-Blue cells as described (Example VIII). Based on colony-forming units (CFU), the number of transformants obtained from each pool was as follows: 2.4X10 6 from pH0707A, 1.8x10 6 from pH0707B, 1.6x10 6 from pH0707C, 8x10 s from pH0707D, 3x10 s from pH0707E, and 4x10 s from pH0707F.
- hGH-phagemid partides were prepared and selected for hGHbp-bind ⁇ ng over 2 to 7 cydes as described in Example VIII. Rapfti sorting of hQH-phagemld libraries
- the pharmacological properties of a protein may be dependent on binding affinity or on kon or koff, depending on the detailed mechanism of action.
- hGH variants with higher on-rates to investigate the effects of changes in kon-
- the selection could altemativety be weighted toward koff by increasing the binding time and increasing the wash time and/or concentration with cognate ligand (hGH).
- phagemid particles from the pH0707B pool were incubated with immobilized hGHbp for only 1 minute, then washed six times with 1 mL of binding buffer; the tiGH-wash step was omitted; and the remaining hGH-phagemid partides were eluted with a pH2 (0.2M glydne in binding buffer) wash. Enrichment of hGH-phagemid partides over non-displaying partides indicated that even with a short binding period and no cognate-ligand (hGH) challenge, hGH-phagemid binding selection sorts tight-binding variants out of a randomized pool. Assay of hGH mutants
- the binding constants for some of these mutants of hGH to hGHbp was determined by expressing the free hormone variants in the non-suppressor £ coli strain 16C9 or 34B8, purifying the protein, and assaying by competitive displacement of labelled wt-hGH from hGHbp (see Example VIII) in a radio-immunoprecipitation assay.
- Table XIII -A below, all the variants have glutamatei74 replaced by serinei74 and phenylalaninei76 replaced by tyrosinei76 (E174S and F1176Y) plus the additional substitutions as indicated at hGH amino add positions 10, 14, 18, 21, 167, 171, 175 and 179.
- hGH variants were selected from combinatorial libraries by the phagemid binding selection process. All hGH variants in Table XIV contain two background mutations (E174S/F176Y). hGH- phagemid pools from the libraries pH0707A (Part A), pH0707B and pH0707E (Part B), or pH0707C (Part C) were sorted for 2 to 7 cydes for binding to hGHbp. The number £ indicates the fractional occurrence of each variant type among the set of clones sequenced from each pool.
- hGH variants were selected from combinatorial libraries by the phagemid binding selection process. All hGH variants in Table XV contain two background mutations (E174S/F176Y). The number £ is the fractional occurrence of a given variant among all dones sequenced after 4 cycles of rapid-binding selection. Table XV hGH variants from RAPID hGHbp binding selection of an hGH-phagemid combinatorial library
- t also contained the mutation Y176F (wild-type hGH also contains F176).
- binding constants were measured by competitive displacement of 12 l-labelled hormone H0650BD or labelled hGH using hGHbp (1-238) and either Mab5 or Mab263.
- the variant H0650BD appears bind more than 30-fold tighter than wild-type hGH.
- the plasmid pS0132 contains the gene for hGH fused to the residue Pro198 of the gene III protein with the insertion of an extra glydne residue.
- This plasmid may be used to produce hGH-phage particles in which the hGH-gene III fusion product is displayed monovalently on the phage surface (Example IV).
- the fusion protein comprises the entire hGH protein fused to the carboxy terminal domain of gene III via a flexible linker sequence.
- a genetically engineered variant of subtilisin BPN' was used. (Carter, P.
- A64SAL subtilisin contains the following mutations: Ser24Cys, His64Ala, Glu156Ser, Gly 169 Ala and Tyr217Leu. Since this enzyme lacks the essential catalytic residue His64, its substrate specificity is greatly restricted so that certain histidine-containing substrates are preferentialty hyrdrolysed (Carter et al., Science 237:394-399 (1987)). Construction of a hGH-substrate-Phage vector
- the sequence of the linker region in pS0132 was mutated to create a substrate sequence for A64SAL subtilisin, using the oligonucleotide 5'-TTC-GGG-CCC-TTC-GCT-GCT-CAC-TAT-ACG-CGT-CAG-TCG- ACT-GAC-CTG-CCT-3'.
- the sequence Ala-Ala-His-Tyr-Thr-Agr-GIn is known to be a good substrate for A64SAL subtilisin (Carter et al (1989), supra).
- the resulting plasmid was designated pS0640.
- Phagemid particles derived from pS0132 and pS0640 were constructed as described in Example I.
- a 10 ⁇ l aliquot of each phage pool was separately mixed with 30 ⁇ l of oxirane beads (prepared as described in Example II) in 100 ⁇ J of buffer comprising 20mM Tris-HCI pH 8.6 and 2.5M NaCl.
- the binding and washing steps were performed as described in example Vll.
- the beads were then resuspended in 400 ⁇ l of the same buffer, with or without 50nM of A64SAL subtilisin. Following incubation for 10 minutes, the supernatants were collected and the phage titres (cfu) measured.
- Table XVli shows that approximately 10 times more substrate-containing phagemid particles (pS0640) were eluted in the presence of enzyme than in the absence of enzyme, or than in the case of the non-substrate phagemids (pS0132) in the presence or absence of enzyme. Increasing the enzyme, phagemid or bead concentrations did not improve this ratio.
- hGH hGH variant used was as described in example XI (pH0650bd) and contains the mutations PhelOAIa, et14Trp, His18Asp, His21Asn, Arg167Asn, Asp171Ser, Glu174Ser, Phe176Tyr and lle179Thr.
- Table XVII shows that there was a dramatic increase in the ratio of specifically eluted substrate-phagemid particles compared to the method previously described for pS0640 and pS0132. It is likely that this is due to the fact that the tight-binding hGH mutant has a significantly slower off-rate for binding to hGH binding protein compared to wild-type hGH.
- Colony forming units were estimated by plating out 10 ⁇ l of 10-fold dilutions of phage on 10 ⁇ l spots of XL-1 blue cells, on LB agar plates containing 50 ⁇ g/ml carbeni ⁇ ' llinl
- pH0650bd mutant hGH gene binding to hGHbp-coated plates phagemid + SQnM AS4SAL no enzyme pDM0411 (substrate) 1.7x10 5 cfu/10 ⁇ i 2x10 3 cfu/10 ⁇ l pDM0390 (non-substrate) 2x10 3 cfu/10 ⁇ l 1x10 3 cfu/10 ⁇ l
- Example XIII We sought to employ the selective enrichment procedure described in Example XIII to identify good substrate sequences from a library of random substrate sequences.
- pDM0253 This new construct was designated pDM0253 (The actual sequence of pDM0253 is 5'-AGC-TGT-GGC-TTC-GGG-CCC-GCC-J2CC-GCG-TCG-ACT-GGC-GGT-GGC-TCT-3', where the underiined base substitution is due to a spurious error in the mutagenic oligonucleotide).
- the tight-binding hGH variant described in example was introduced by exchanging a fragment from pDM0411 (example XIII) The resulting library vector was designated pDM0454.
- pD 0454 was digested with Apal followed by Sail, then precipitated with 13% PEG 8000+ 10m MgCfc, washed twice in 70% ethanol and resuspended This efficiently precipitates the vector but leaves the small Apa-Sal fragment in solution (Pai thankar, K. R. and Prasad, K. S. N., Nucleic Acids Research 19:1346).
- the product was run on a 1% agarose gel and the Apal-Sall digested vector excised, purified using a Bandprep kit (Pharmacia) and resuspended for ligation with the mutagenic cassette.
- the cassette to be inserted contained a DNA sequence similar to that in the linker region of pS0640 and pD 0411 , but with the codons for the histidine and tyrosine residues in the substrate sequence replaced by randomised codons.
- the oligonucleotides used in the mutagenic cassettes were: 5'-C-TTC-GCT-GCT-NNS-NNS-ACC- CGG-CAA-3' (coding strand) and 5'-T-CGA-TTG-CCG-GGT-SNN-SNN-AGC-AGC-GAA-GGG- CC-3' (non-coding strand).
- This cassette also destroys the Sail site, so that digestion with Sail may be used to reduce the vector background.
- the oligonucleotides were not phosphorylated before insertion into the Apa-Sai cassette site, as it was feared that subsequent oligomerisation of a small population of the cassettes may lead to spurious results with multiple cassette inserts.
- reaction products were phenohchloroform extracted, ethanol precipitated and resuspended in water. Initially, no digestion with Sail to reduce the background vector was performed. Approximately 200 ng was electroporated into XL-1 blue cells and a phagemid library was prepared as described in example VIII.
- the selection procedure used was identical to that described for pDM0411 and pDM0390 in example XIII. After each round of selection, the eluted phage were propagated by transducing a fresh culture of XL-1 blue cells and propagating a new phagemid library as described for hGH-phage in example VIII. The progress of the selection procedure was monitored by measuring eluted phage titres and by sequencing individual clones after each round of selection.
- Table A shows the successive phage titres for elution in the presence and absence of enzyme after 1 , 2 and 3 rounds of selection.
- the ratio of specifically eluted phage: non-specifically eluted phage increases dramatically from round 1 to round 3, suggesting that the population of good substrates is increasing with each round of selection.
- Sequencing of 10 isolates from the starting library showed them all to consist of the wild-type pD 0464 sequence. This is attributed to the fact that after digestion with Apal, the Sail site is very close to the end of the DNA fragment, thus leading to low efficiency of digestion. Nevertheless, there are only 400 possible sequences in the library, so this population should still be well represented.
- Tables B1 and B2 shows the sequences of isolates obtained after round 2 and round 3 of selection. After 2 rounds of selection, there is clearly a high incidence of histidine residues. This is exactly what is expected: as described in example XIII, A64SAL subtilisin requires a histidine residue in the substrate as it employs a substrate-assisted catalytic mechanism. After 3 rounds of selection, each of the 10 clones sequenced has a histidine in the randomised cassette. Note, however, that 2 of the sequences are of pDM0411 , which was not present in the starting library and is therefore a contaminant.
- Colony forming units were estimated by plating out 10 ⁇ l of 10-fold dilutions of phage on 10 ⁇ l spots of XL-1 blue cells, on LB agar plates containing 50 ⁇ g ml carbenidiiin
- GCT GCT CAC ATG ACC CGG CAA ...
- GATCTGCACT GCACSNNGCG CAGGTASNNG CTGACCTTSN NCATGTCCTT 50
- ACGCAAGTTC ACGTAAAAAG GGTATCTAGA GGTTGAGGTG ATTTTATGAA 800 AAAGAATATC GCATTTCTTC TTGCATCTAT GTTCGTTTTT TCTATTGCTA 850
- Met Lys Lys Asn lie Ala Phe Leu Leu Ala Ser Met Phe Val Phe 1 5 10 15
Abstract
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EP92902109A EP0564531B1 (en) | 1990-12-03 | 1991-12-03 | Enrichment method for variant proteins with altered binding properties |
JP50271092A JP3267293B2 (en) | 1990-12-03 | 1991-12-03 | Methods for enriching mutant proteins with altered binding |
CA002095633A CA2095633C (en) | 1990-12-03 | 1991-12-03 | Enrichment method for variant proteins with altered binding properties |
ES92902109T ES2113940T3 (en) | 1990-12-03 | 1991-12-03 | ENRICHMENT METHOD FOR PROTEIN VARIANTS WITH ALTERED UNION PROPERTIES. |
DK92902109T DK0564531T3 (en) | 1990-12-03 | 1991-12-03 | Enrichment procedure for variant proteins with altered binding properties |
US08/050,058 US5750373A (en) | 1990-12-03 | 1991-12-03 | Enrichment method for variant proteins having altered binding properties, M13 phagemids, and growth hormone variants |
DE69129154T DE69129154T2 (en) | 1990-12-03 | 1991-12-03 | METHOD FOR ENRICHING PROTEIN VARIANTS WITH CHANGED BINDING PROPERTIES |
US08/463,667 US5834598A (en) | 1990-12-03 | 1995-06-05 | Human growth hormone variants |
US08/463,587 US5821047A (en) | 1990-12-03 | 1995-06-05 | Monovalent phage display |
GR980400652T GR3026468T3 (en) | 1990-12-03 | 1998-03-27 | Enrichment method for variant proteins with altered binding properties |
US11/199,062 US20060115874A1 (en) | 1990-12-03 | 2005-08-08 | Enrichment method for variant proteins with altered binding properties |
US11/761,180 US20080038717A1 (en) | 1990-12-03 | 2007-06-11 | Enrichment method for variant proteins with altered binding properties |
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WO2002100330A2 (en) | 2001-06-08 | 2002-12-19 | Abbott Biotechnology Ltd | METHODS OF ADMINISTERING ANTI-TNFα ANTIBODIES |
US6497874B1 (en) | 1997-02-05 | 2002-12-24 | Maardh Sven | Recombinant phages |
WO2003040170A2 (en) | 2001-11-09 | 2003-05-15 | Pfizer Products Inc. | Antibodies to cd40 |
US6573370B1 (en) | 2000-05-19 | 2003-06-03 | Regents Of The University Of Michigan | PON3 and uses thereof |
US6616926B1 (en) | 1999-03-03 | 2003-09-09 | Curis, Inc. | Methods of modulating lipid metabolism and storage |
WO2003082914A1 (en) | 2002-04-03 | 2003-10-09 | The University Of Queensland | Prothrombin activating protein |
US6632645B1 (en) | 2000-03-02 | 2003-10-14 | Promega Corporation | Thermophilic DNA polymerases from Thermoactinomyces vulgaris |
US6667150B1 (en) | 1997-08-01 | 2003-12-23 | Morphosys Ag | Method and phage for the identification of nucleic acid sequences encoding members of a multimeric (poly) peptide complex |
US6777194B1 (en) | 1999-04-01 | 2004-08-17 | Dakocytomation Denmark A/S | Monoclonal antibodies against human protein Mcm3, process for their production, and their use |
US6800740B1 (en) | 1991-05-10 | 2004-10-05 | Genentech, Inc. | Variants of native growth hormones having non naturally occurring amino acid sequences or covalent modifications |
US6806079B1 (en) | 1990-07-10 | 2004-10-19 | Medical Research Council | Methods for producing members of specific binding pairs |
US6878861B2 (en) | 2000-07-21 | 2005-04-12 | Washington State University Research Foundation | Acyl coenzyme A thioesterases |
WO2004094476A3 (en) * | 2003-04-16 | 2005-06-16 | Genentech Inc | Compositions and methods relating to stop-1 |
US6914128B1 (en) | 1999-03-25 | 2005-07-05 | Abbott Gmbh & Co. Kg | Human antibodies that bind human IL-12 and methods for producing |
US6951839B1 (en) | 1999-11-30 | 2005-10-04 | Curis, Inc. | Methods and compositions for regulating lymphocyte activity |
EP1592777A2 (en) * | 2003-02-01 | 2005-11-09 | Tanox, Inc. | A method for generating high affinity antibodies |
WO2006014744A2 (en) | 2004-07-23 | 2006-02-09 | University Of Massachusetts | Compounds that inhibit hsp90 protein-protein interactions with iap proteins |
EP1626056A2 (en) | 1999-12-30 | 2006-02-15 | President And Fellows of Harvard College | Methods and compositions relating to modulation of hepatocyte growth, plasma cell differentiation or T cell subset activity by modulation of XBP-1 activity |
US7037498B2 (en) | 2001-01-05 | 2006-05-02 | Abgenix, Inc. | Antibodies to insulin-like growth factor I receptor |
US7056517B2 (en) | 1998-04-13 | 2006-06-06 | The Forsyth Institute | Glucosyltransferase immunogens |
US7063943B1 (en) | 1990-07-10 | 2006-06-20 | Cambridge Antibody Technology | Methods for producing members of specific binding pairs |
US7087418B2 (en) | 2001-12-19 | 2006-08-08 | Bristol-Myers Squibb Company | Pichia pastoris formate dehydrogenase and uses therefor |
US7101549B2 (en) | 1999-06-30 | 2006-09-05 | Millennium Pharmaceuticals, Inc. | Glycoprotein VI and uses thereof |
EP1714661A2 (en) | 2000-05-19 | 2006-10-25 | The Center for Blood Research, INC. | Methods for diagnosing and treating hemostatic disorders by modulating p-selectin activity |
WO2006116442A2 (en) | 2005-04-27 | 2006-11-02 | Tripath Imaging, Inc. | Monoclonal antibodies and methods for their use in the detection of cervical disease |
US7151169B2 (en) | 1999-04-30 | 2006-12-19 | Cambridge Antibody Technology Limited | Specific binding members for TGFβ1 |
US7163682B2 (en) | 1998-04-13 | 2007-01-16 | The Forsyth Institute | Glucan binding protein and glucosyltransferase immunogens |
WO2007024715A2 (en) | 2005-08-19 | 2007-03-01 | Abbott Laboratories | Dual variable domain immunoglobin and uses thereof |
WO2007024705A2 (en) | 2005-08-19 | 2007-03-01 | Abbott Biotechnology Ltd. | Method of treating depression using a tnf-alpha antibody |
US7250551B2 (en) | 2002-07-24 | 2007-07-31 | President And Fellows Of Harvard College | Transgenic mice expressing inducible human p25 |
WO2007089303A2 (en) | 2005-11-01 | 2007-08-09 | Abbott Biotechnology Ltd. | Methods and compositions for diagnosing ankylosing spondylitis using biomarkers |
US7323175B2 (en) | 2002-03-07 | 2008-01-29 | The Forsyth Institute | Immunogenicity of glucan binding protein |
US7326414B2 (en) | 2003-09-10 | 2008-02-05 | Warner-Lambert Company Llc | Antibodies to M-CSF |
WO2008052187A2 (en) | 2006-10-27 | 2008-05-02 | Genentech. Inc. | Antibodies and immunoconjugates and uses therefor |
US7368111B2 (en) | 1995-10-06 | 2008-05-06 | Cambridge Antibody Technology Limited | Human antibodies specific for TGFβ2 |
US7378506B2 (en) | 1997-07-21 | 2008-05-27 | Ohio University | Synthetic genes for plant gums and other hydroxyproline-rich glycoproteins |
US7396905B1 (en) | 1999-05-21 | 2008-07-08 | Mckeon Frank | Calcipressins: endogenous inhibitors of calcineurin, uses and reagents related thereto |
WO2008083174A2 (en) | 2006-12-27 | 2008-07-10 | Emory University | Compositions and methods for the treatment of infections and tumors |
EP1944322A2 (en) | 2002-07-19 | 2008-07-16 | Abbott Biotechnology Ltd. | Treatment of TNF alpha related disorders |
US7405276B2 (en) | 2000-11-01 | 2008-07-29 | Elusys Therapeutics, Inc. | Method of producing bispecific molecules by protein trans-splicing |
EP1958966A2 (en) | 1994-07-01 | 2008-08-20 | Dana-Farber Cancer Institute | Methods for modulating T cell responses by manipulating a common cytokine receptor gamma chain |
EP1975620A2 (en) | 2001-03-02 | 2008-10-01 | GPC Biotech AG | Three hybrid assay system |
EP1990409A2 (en) | 1999-07-20 | 2008-11-12 | MorphoSys AG | Bacteriophage |
US7455989B2 (en) | 2002-08-20 | 2008-11-25 | Yeda Research And Development Co. Ltd. | AKAP84 and its use for visualization of biological structures |
US7465705B2 (en) | 2002-08-10 | 2008-12-16 | Yale University | Nogo receptor antagonists |
WO2008151819A2 (en) | 2007-06-15 | 2008-12-18 | Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts | Treatment of tumors using specific anti-l1 antibody |
WO2008154543A2 (en) | 2007-06-11 | 2008-12-18 | Abbott Biotechnology Ltd. | Methods for treating juvenile idiopathic arthritis |
US7488807B2 (en) | 2006-11-22 | 2009-02-10 | 3M Innovative Properties Company | Antibody with protein A selectivity |
US7491516B2 (en) | 2000-06-29 | 2009-02-17 | Abbott Laboratories | Dual specificity antibodies and methods of making and using |
WO2009024593A1 (en) | 2007-08-21 | 2009-02-26 | Morphosys Ag | Improved methods for the formation of disulphide bonds |
US7498420B2 (en) | 2003-08-04 | 2009-03-03 | Amgen Fremont Inc. | Antibodies to c-Met |
EP2033662A1 (en) | 2004-01-21 | 2009-03-11 | Novo Nordisk Health Care AG | Transglutaminase mediated conjugation of peptides |
EP2051077A2 (en) | 2003-10-07 | 2009-04-22 | Millennium Pharmaceuticals, Inc. | Nucleic acid molecules and proteins for the identification, assessment, prevention, and therapy of ovarian cancer |
EP2060628A1 (en) | 2002-02-13 | 2009-05-20 | XOMA Technology Ltd. | Eukaryotic signal sequences for polypeptide expression and polypeptide display libraries |
US7537762B2 (en) | 2005-09-07 | 2009-05-26 | Amgen Fremont, Inc. | Human monoclonal antibodies to activin receptor-like kinase-1 |
EP2065402A1 (en) | 2007-11-30 | 2009-06-03 | Industrial Technology Research Institut | Trimeric collagen scaffold antibodies |
EP2065467A2 (en) | 2001-02-22 | 2009-06-03 | Genentech, Inc. | Anti-interferon-alpha antibodies |
US7550280B2 (en) | 2002-08-19 | 2009-06-23 | Dsm Ip Assets B.V. | Lipases and uses thereof |
EP2077324A2 (en) | 2001-02-23 | 2009-07-08 | DSM IP Assets B.V. | Genes encoding proteolytic enzymes from aspargilli |
WO2009086003A1 (en) | 2007-12-20 | 2009-07-09 | Xoma Technology Ltd. | Methods for the treatment of gout |
WO2009086539A2 (en) | 2007-12-28 | 2009-07-09 | Elan Pharmaceuticals, Inc. | Treatment and prophylaxis of amyloidosis |
US7572886B2 (en) | 2001-12-18 | 2009-08-11 | Centre National De La Recherche Scientifique | Death associated proteins, and THAP1 and PAR4 pathways in apoptosis control |
WO2009109572A2 (en) * | 2008-03-03 | 2009-09-11 | Ablynx Nv | Monovalent phage display of single variable domains |
US7588925B2 (en) | 2002-05-21 | 2009-09-15 | Dsm Ip Assets B.V. | Phospholipases and uses thereof |
US7612181B2 (en) | 2005-08-19 | 2009-11-03 | Abbott Laboratories | Dual variable domain immunoglobulin and uses thereof |
EP2113255A1 (en) | 2008-05-02 | 2009-11-04 | f-star Biotechnologische Forschungs- und Entwicklungsges.m.b.H. | Cytotoxic immunoglobulin |
EP2116556A1 (en) | 2008-05-09 | 2009-11-11 | Abbott GmbH & Co. KG | Antibodies to receptor of advanced glycation end products (rage) and uses thereof |
US7618626B2 (en) | 2004-07-16 | 2009-11-17 | Pfizer Inc | Combination treatment for non-hematologic malignancies |
WO2009149185A2 (en) | 2008-06-03 | 2009-12-10 | Abbott Laboratories | Dual variable domain immunoglobulins and uses thereof |
EP2133427A1 (en) | 2004-01-14 | 2009-12-16 | Ohio University | Methods of producing peptides/proteins in plants and peptides/proteins produced thereby |
US7667099B2 (en) | 2002-06-20 | 2010-02-23 | Board Of Trustees Of Michigan State University | Plastid division and related genes and proteins, and methods of use |
EP2168984A1 (en) | 1999-03-25 | 2010-03-31 | Abbott GmbH & Co. KG | Human antibodies that bind human IL-12 and methods for producing |
WO2010039533A2 (en) | 2008-09-23 | 2010-04-08 | Wyeth | Methods for predicting production of activating signals by cross-linked binding proteins |
WO2010039536A2 (en) | 2008-09-23 | 2010-04-08 | President And Fellows Of Harvard College | Sirt4 and uses thereof |
US7700739B2 (en) | 2005-06-30 | 2010-04-20 | Abbott Laboratories | IL-12/p40 binding proteins |
EP2177537A2 (en) | 2004-01-09 | 2010-04-21 | Pfizer Inc. | Antibodies to MAdCAM |
WO2010045315A1 (en) | 2008-10-14 | 2010-04-22 | Dyax Corp. | Use of igf-ii/igf-iie binding for the treatment and prevention of systemic sclerosis associated pulmonary fibrosis |
EP2181711A1 (en) | 2002-09-04 | 2010-05-05 | Biopolymer Engineering, Inc. | Cancer therapy using whole glucan particles and antibodies |
WO2010062995A2 (en) | 2008-11-26 | 2010-06-03 | Five Prime Therapeutics, Inc. | Compositions and methods for regulating collagen and smooth muscle actin expression by serpine2 |
WO2010063011A2 (en) | 2008-11-28 | 2010-06-03 | Emory University | Methods for the treatment of infections and tumors |
EP2196218A2 (en) | 2002-04-26 | 2010-06-16 | Abbott Biotechnology Ltd | Use of anti-TNFalpha antibodies and another drug |
US7745391B2 (en) | 2001-09-14 | 2010-06-29 | Compugen Ltd. | Human thrombospondin polypeptide |
US7744890B2 (en) | 2006-10-12 | 2010-06-29 | Wyeth Llc | Methods and compositions with reduced opalescence |
WO2010080985A1 (en) | 2009-01-08 | 2010-07-15 | Dana-Farber Cancer Institute, Inc. | Compositions and methods for induced brown fat differentiation |
WO2010084173A1 (en) | 2009-01-22 | 2010-07-29 | Novo Nordisk Health Care Ag | Stable growth hormone compounds |
EP2216653A1 (en) | 2005-08-02 | 2010-08-11 | XBiotech, Inc | Diagnosis, treatment and prevention of vascular disorders using il-1alpha autoantibodies |
US7776331B1 (en) | 2007-01-16 | 2010-08-17 | Abbott Laboratories | Methods of treating plaque psoriasis |
WO2010099079A1 (en) | 2009-02-24 | 2010-09-02 | Abbott Laboratories | Antibodies to troponin i and methods of use thereof |
WO2010102177A1 (en) | 2009-03-06 | 2010-09-10 | Becton, Dickinson And Company | Glycodelin monoclonal antibodies and methods for their use in the detection of ovarian cancer |
WO2010102167A1 (en) | 2009-03-05 | 2010-09-10 | Becton, Dickinson And Company | Matrix metalloproteinase-7 (mmp-7) monoclonal antibodies and methods for their use in the detection of ovarian cancer |
US7795494B2 (en) | 2001-03-22 | 2010-09-14 | Abbott Laboratories | Transgenic mice expressing antibodies specific for genes of interest and uses thereof |
US7803377B2 (en) | 2006-06-06 | 2010-09-28 | Genentech, Inc. | Anti-DLL4 antibodies and methods using same |
WO2010111367A1 (en) | 2009-03-25 | 2010-09-30 | Genentech, Inc. | Anti-fgfr3 antibodies and methods using same |
US7807790B2 (en) | 2005-11-14 | 2010-10-05 | Metamol Theranostics, Llc | Peptide sequence that promotes tumor invasion |
WO2010120561A1 (en) | 2009-04-01 | 2010-10-21 | Genentech, Inc. | Anti-fcrh5 antibodies and immunoconjugates and methods of use |
EP2251026A1 (en) | 2000-06-08 | 2010-11-17 | Immune Disease Institute, Inc. | Methods and compositions for inhibiting immunoglobulin-mediated reperfusion injury |
US7846439B2 (en) | 2006-02-01 | 2010-12-07 | Cephalon Australia Pty Ltd | Domain antibody construct |
EP2258718A1 (en) | 2001-04-16 | 2010-12-08 | Wyeth Holdings Corporation | Streptococcus pneumoniae open reading frames encoding polypeptide antigens and uses thereof |
EP2261242A1 (en) | 2009-06-10 | 2010-12-15 | Universite Catholique De Louvain | Aspartate-N-acetyltransferase enzyme, diagnostic method and therapeutic method |
US7858297B2 (en) | 2001-12-18 | 2010-12-28 | Centre National De La Recherche Scientifique Cnrs | Chemokine-binding protein and methods of use |
EP2270188A2 (en) | 2001-06-22 | 2011-01-05 | Pioneer Hi-Bred International, Inc. | Defensin polynucleotides and methods of use |
EP2270034A2 (en) | 2004-06-03 | 2011-01-05 | Athlomics Pty Ltd | Agents and methods for diagnosing stress |
US7867494B2 (en) | 2007-04-02 | 2011-01-11 | Amgen Fremont Inc. | Anti-IgE antibodies |
EP2272979A1 (en) | 2009-06-30 | 2011-01-12 | Centre National de la Recherche Scientifique (CNRS) | Method for testing a subject thought to be predisposed to having cancer |
WO2011003996A1 (en) | 2009-07-09 | 2011-01-13 | F. Hoffmann-La Roche Ag | In vivo tumor vasculature imaging |
WO2011014457A1 (en) | 2009-07-27 | 2011-02-03 | Genentech, Inc. | Combination treatments |
US7883704B2 (en) | 1999-03-25 | 2011-02-08 | Abbott Gmbh & Co. Kg | Methods for inhibiting the activity of the P40 subunit of human IL-12 |
EP2290107A1 (en) | 2003-01-07 | 2011-03-02 | Dyax Corporation | Kunitz domain library |
EP2290086A2 (en) | 2004-12-22 | 2011-03-02 | Genentech, Inc. | Methods for producing soluble multi-membrane-spanning proteins |
EP2289909A1 (en) | 2005-11-30 | 2011-03-02 | Abbott Laboratories | Screening method, process for purifying of non-diffusible a-beta oligomers, selective antibodies against said non-diffusible a-beta oligomers and a process for manufacturing of said antibodies |
EP2290077A2 (en) | 2004-03-01 | 2011-03-02 | Immune Disease Institute, Inc. | Natural IGM antibodies and inhibitors thereof |
WO2011025964A2 (en) | 2009-08-29 | 2011-03-03 | Abbott Laboratories | Therapeutic dll4 binding proteins |
EP2293069A2 (en) | 2004-03-24 | 2011-03-09 | Tripath Imaging, Inc. | Methods and compositions for the detection of cervical disease |
WO2011028950A1 (en) | 2009-09-02 | 2011-03-10 | Genentech, Inc. | Mutant smoothened and methods of using the same |
EP2295466A2 (en) | 2005-04-25 | 2011-03-16 | Pfizer Inc. | Antibodies to myostatin |
EP2295606A1 (en) | 2000-11-28 | 2011-03-16 | Wyeth LLC | Expression analysis of KIAA nucleic acids and polypeptides useful in the diagnosis and treatment of prostate cancer |
EP2298899A2 (en) | 1997-04-16 | 2011-03-23 | Millennium Pharmaceuticals, Inc. | CRSP proteins (cysteine-rich secreted proteins), nucleic acid molecules encoding them and uses therefor |
WO2011035205A2 (en) | 2009-09-18 | 2011-03-24 | Calmune Corporation | Antibodies against candida, collections thereof and methods of use |
EP2301947A2 (en) | 1999-02-26 | 2011-03-30 | Millennium Pharmaceuticals, Inc. | Secreted proteins and uses thereof |
WO2011038301A2 (en) | 2009-09-25 | 2011-03-31 | Xoma Technology Ltd. | Screening methods |
WO2011038290A2 (en) | 2009-09-25 | 2011-03-31 | The U. S. A., As Represented By The Secretary, Department Of Health And Human Services | Neutralizing antibodies to hiv-1 and their use |
WO2011038302A2 (en) | 2009-09-25 | 2011-03-31 | Xoma Technology Ltd. | Novel modulators |
WO2011036555A1 (en) | 2009-09-25 | 2011-03-31 | University Of Oslo | Multivalent phage display systems and methods |
US7919257B2 (en) | 2003-05-30 | 2011-04-05 | Merus Biopharmaceuticals, B.V.I.O. | Method for selecting a single cell expressing a heterogeneous combination of antibodies |
EP2305836A1 (en) | 2002-08-20 | 2011-04-06 | Millennium Pharmaceuticals, Inc. | Compositions, kits and methods for identification, assessment, prevention and therapy of cervical cancer |
EP2305713A1 (en) | 1996-02-09 | 2011-04-06 | Abbott Biotechnology Ltd | Human antibodies that bind human TNFalpha |
WO2011041584A2 (en) | 2009-09-30 | 2011-04-07 | President And Fellows Of Harvard College | Methods for modulation of autophagy through the modulation of autophagy-enhancing gene products |
US7927834B2 (en) | 2002-07-18 | 2011-04-19 | Merus B.V. | Recombinant production of mixtures of antibodies |
WO2011050188A1 (en) | 2009-10-22 | 2011-04-28 | Genentech, Inc. | Anti-hepsin antibodies and methods using same |
EP2316969A1 (en) | 2003-03-13 | 2011-05-04 | Fujirebio America, Inc. | Detection of urinary mesothelin-/megakaryocyte potentiating factor-related peptides for assessment of ovarian cancer |
EP2316976A1 (en) | 2000-11-28 | 2011-05-04 | Wyeth LLC | Expression analysis of FKBP nucleic acids and polypeptides useful in the diagnosis and treatment of prostate cancer |
WO2011053538A1 (en) | 2009-10-27 | 2011-05-05 | Exxonmobil Research And Engineering Company | Multi-stage processes and control thereof |
WO2011057120A1 (en) | 2009-11-05 | 2011-05-12 | Genentech, Inc. | Methods and composition for secretion of heterologous polypeptides |
WO2011056497A1 (en) | 2009-10-26 | 2011-05-12 | Genentech, Inc. | Activin receptor type iib compositions and methods of use |
WO2011056494A1 (en) | 2009-10-26 | 2011-05-12 | Genentech, Inc. | Activin receptor-like kinase-1 antagonist and vegfr3 antagonist combinations |
WO2011056502A1 (en) | 2009-10-26 | 2011-05-12 | Genentech, Inc. | Bone morphogenetic protein receptor type ii compositions and methods of use |
WO2011058087A1 (en) | 2009-11-11 | 2011-05-19 | Gentian As | Immunoassay for assessing related analytes of different origin |
EP2325208A1 (en) | 2005-12-15 | 2011-05-25 | Genentech, Inc. | Polyubiquitin antibodies |
EP2327423A2 (en) | 2006-02-21 | 2011-06-01 | Wyeth LLC | Human antibodies against human interleukin-22 (IL-22) |
WO2011070045A1 (en) | 2009-12-08 | 2011-06-16 | Abbott Gmbh & Co. Kg | Monoclonal antibodies against the rgm a protein for use in the treatment of retinal nerve fiber layer degeneration |
WO2011071577A1 (en) | 2009-12-11 | 2011-06-16 | Genentech, Inc. | Anti-vegf-c antibodies and methods using same |
US7964708B2 (en) | 2006-11-15 | 2011-06-21 | Limin Li | Anti-TSG101 antibodies and their uses for treatment of viral infections |
EP2335731A2 (en) | 2004-04-09 | 2011-06-22 | Abbott Biotechnology Ltd | Multiple-variable dose regimen for treating TNF-alpha-related disorders |
EP2336170A2 (en) | 2005-12-15 | 2011-06-22 | Industrial Technology Research Institute | Recombinant triplex scaffold-based polypeptides |
EP2336160A2 (en) | 2003-01-31 | 2011-06-22 | Abbott GmbH & Co. KG | Amyloid-beta(1-42) oligomers, derivatives thereof, antibodies for the same, method for production and use thereof. |
WO2011079185A1 (en) | 2009-12-23 | 2011-06-30 | Genentech, Inc. | Anti-bv8 antibodies and uses thereof |
WO2011084750A1 (en) | 2009-12-21 | 2011-07-14 | Genentech, Inc. | Antibody formulation |
WO2011085103A2 (en) | 2010-01-06 | 2011-07-14 | Dyax Corp. | Plasma kallikrein binding proteins |
WO2011088163A1 (en) | 2010-01-14 | 2011-07-21 | President And Fellows Of Harvard College | Methods for modulating skeletal remodeling and patterning by modulating shn2 activity, shn3 activity, or shn2 and shn3 activity in combination |
WO2011089250A2 (en) | 2010-01-22 | 2011-07-28 | Novo Nordisk Health Care Ag | Stable growth hormone compounds |
WO2011091134A2 (en) | 2010-01-22 | 2011-07-28 | Dana-Farber Cancer Institute, Inc. | Compositions,kits, and methods for identification, assessment, prevention, and therapy of metabolic disorders |
WO2011097301A2 (en) | 2010-02-02 | 2011-08-11 | Abbott Biotechnology Ltd. | METHODS AND COMPOSITIONS FOR PREDICTING RESPONSIVENESS TO TREATMENT WITH TNF-α INHIBITOR |
WO2011095894A2 (en) | 2010-02-04 | 2011-08-11 | Jichi Medical University | Identification, assessment, and therapy of cancers with innate or acquired resistance to alk inhibitors |
EP2360254A1 (en) | 1999-08-23 | 2011-08-24 | Dana-Farber Cancer Institute, Inc. | Assays for screening anti-pd-1 antibodies and uses thereof |
EP2363711A1 (en) | 2006-01-27 | 2011-09-07 | Tripath Imaging, Inc. | Methods for identifying patients with an increased likelihood of having ovarian cancer and compositions therefor |
WO2011119484A1 (en) | 2010-03-23 | 2011-09-29 | Iogenetics, Llc | Bioinformatic processes for determination of peptide binding |
WO2011130377A2 (en) | 2010-04-15 | 2011-10-20 | Abbott Laboratories | Amyloid-beta binding proteins |
EP2385070A1 (en) | 2003-11-12 | 2011-11-09 | Abbott Laboratories | Il-18 binding proteins |
EP2386318A1 (en) | 2003-05-15 | 2011-11-16 | Iogenetics, Inc. | Targeted biocides |
WO2011143562A2 (en) | 2010-05-14 | 2011-11-17 | Abbott Laboratories | Il-1 binding proteins |
EP2388274A1 (en) | 2005-06-17 | 2011-11-23 | Janssen Alzheimer Immunotherapy | Methods of purifying anti A Beta antibodies |
EP2388590A1 (en) | 2001-04-02 | 2011-11-23 | Dana Farber Cancer Institute | PD-1, a receptor for B7-4, and uses thereof |
EP2392353A1 (en) | 2005-01-28 | 2011-12-07 | Janssen Alzheimer Immunotherapy | Anti A beta antibody formulation |
WO2011153346A1 (en) | 2010-06-03 | 2011-12-08 | Genentech, Inc. | Immuno-pet imaging of antibodies and immunoconjugates and uses therefor |
WO2011153477A2 (en) | 2010-06-03 | 2011-12-08 | Abbott Biotechnology Ltd. | Uses and compositions for treatment of hidradenitis suppurativa (hs) |
EP2395077A1 (en) | 2006-11-03 | 2011-12-14 | Wyeth LLC | Glycolysis-inhibiting substances in cell culture |
EP2402438A2 (en) | 2006-07-05 | 2012-01-04 | Catalyst Biosciences, Inc. | Protease screening methods and proteases identified thereby |
EP2402373A2 (en) | 2006-01-05 | 2012-01-04 | Genentech, Inc. | Anti-EphB4 Antibodies and Methods Using Same |
WO2012006500A2 (en) | 2010-07-08 | 2012-01-12 | Abbott Laboratories | Monoclonal antibodies against hepatitis c virus core protein |
WO2012007880A2 (en) | 2010-07-16 | 2012-01-19 | Ablynx Nv | Modified single domain antigen binding molecules and uses thereof |
EP2410335A1 (en) | 2005-11-30 | 2012-01-25 | Massachusetts Institute of Technology (MIT) | Pathogen detection biosensor |
WO2012010516A1 (en) | 2010-07-22 | 2012-01-26 | Novo Nordisk Health Care Ag | Growth hormone conjugates |
WO2012019061A2 (en) | 2010-08-05 | 2012-02-09 | Stem Centrx, Inc. | Novel effectors and methods of use |
WO2012020072A1 (en) | 2010-08-12 | 2012-02-16 | Westfälische Wilhelms-Universität Muenster | Anti-syndecan-4 antibodies |
WO2012024650A2 (en) | 2010-08-19 | 2012-02-23 | Abbott Laboratories | Anti-ngf antibodies and their use |
WO2012027723A1 (en) | 2010-08-27 | 2012-03-01 | Stem Centrx, Inc | Notum protein modulators and methods of use |
WO2012031273A2 (en) | 2010-09-03 | 2012-03-08 | Stem Centrx, Inc. | Novel modulators and methods of use |
EP2431392A1 (en) | 2006-02-21 | 2012-03-21 | Wyeth LLC | Antibodies against human IL-22 and uses therefor |
WO2012040041A1 (en) | 2010-09-20 | 2012-03-29 | Abbott Laboratories | Purification of antibodies using simulated moving bed chromatography |
WO2012044921A1 (en) | 2010-10-01 | 2012-04-05 | St. Jude Children's Research Hospital | Methods and compositions for typing molecular subgroups of medulloblastoma |
WO2012041981A2 (en) | 2010-09-30 | 2012-04-05 | Laboratorios Del Dr. Esteve, S.A. | Use of growth hormone to enhance the immune response in immunosuppressed patients |
WO2012047324A2 (en) | 2010-06-10 | 2012-04-12 | President And Fellows Of Harvard College | Systems and methods for amplification and phage display |
WO2012047968A2 (en) | 2010-10-05 | 2012-04-12 | Genentech, Inc. | Mutant smoothened and methods of using the same |
EP2441474A1 (en) | 2003-10-17 | 2012-04-18 | Joslin Diabetes Center, Inc. | Methods and compositions for modulating adipocyte function |
EP2444421A1 (en) | 2005-04-26 | 2012-04-25 | Pfizer Inc. | P-Cadherin antibodies |
EP2444805A2 (en) | 2004-01-21 | 2012-04-25 | Fujirebio America, Inc. | Detection of mesothelin-/megakaryocyte potentiating factor-related peptides in peritoneal fluid for assessment of the peritoneum and the peritoneal cavity |
WO2012052391A1 (en) | 2010-10-19 | 2012-04-26 | Glaxo Group Limited | Polypeptide with jmjd3 catalytic activity |
US8168178B2 (en) | 1999-11-30 | 2012-05-01 | Curis, Inc. | Methods and compositions for regulating lymphocyte activity |
US8168760B2 (en) | 2007-03-29 | 2012-05-01 | Abbott Laboratories | Crystalline anti-human IL-12 antibodies |
EP2446904A2 (en) | 2006-05-30 | 2012-05-02 | Genentech, Inc. | Anti-CD22 antibodies, their immunoconjugates and uses thereof |
US8178579B2 (en) | 2001-05-09 | 2012-05-15 | President And Fellows Of Harvard College | Dioxanes and uses thereof |
US8178092B2 (en) | 2008-03-18 | 2012-05-15 | Abbott Laboratories | Methods of treating psoriasis by administration of antibodies to the p40 subunit of IL-12 and/or IL-23 |
EP2455395A1 (en) | 2005-12-19 | 2012-05-23 | Tripath Imaging, Inc. | MCM6 monoclonal antibodies and methods for their use in the detection of cervical disease |
WO2012068463A2 (en) | 2010-11-18 | 2012-05-24 | Beth Israel Deaconess Medicall Center, Inc. | Methods of treating obesity by inhibiting nicotinamide n-methyl transferase (nnmt) |
EP2460832A2 (en) | 2005-05-27 | 2012-06-06 | Biogen Idec MA Inc. | TWEAK binding antibodies |
WO2012078813A2 (en) | 2010-12-08 | 2012-06-14 | Stem Centrx, Inc. | Novel modulators and methods of use |
EP2468772A2 (en) | 2006-03-16 | 2012-06-27 | Genentech, Inc. | Antibodies to EGFL7 and methods for their use |
WO2012088094A2 (en) | 2010-12-21 | 2012-06-28 | Abbott Laboratories | Il-1 binding proteins |
WO2012089814A1 (en) | 2010-12-30 | 2012-07-05 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Antigen binding formats for use in therapeutic treatments or diagnostic assays |
WO2012092539A2 (en) | 2010-12-31 | 2012-07-05 | Takeda Pharmaceutical Company Limited | Antibodies to dll4 and uses thereof |
WO2012092323A1 (en) | 2010-12-28 | 2012-07-05 | Xoma Technology Ltd. | Cell surface display using pdz domains |
EP2474557A2 (en) | 2007-07-16 | 2012-07-11 | Genentech, Inc. | Anti-CD79b antibodies and immunoconjugates and methods of use |
US8222423B2 (en) | 2006-02-14 | 2012-07-17 | Dana-Farber Cancer Institute, Inc. | Bifunctional histone deacetylase inhibitors |
EP2476761A2 (en) | 2005-07-07 | 2012-07-18 | Athlomics Pty Ltd | Polynucleotide marker genes and their expression, for diagnosis of endotoxemia |
EP2481797A1 (en) | 2007-04-13 | 2012-08-01 | Catalyst Biosciences, Inc. | Modified factor VII polypeptides and uses thereof |
WO2012112943A1 (en) | 2011-02-18 | 2012-08-23 | Stem Centrx, Inc. | Novel modulators and methods of use |
WO2012119129A1 (en) | 2011-03-02 | 2012-09-07 | Berg Biosystems, Llc | Interrogatory cell-based assays and uses thereof |
WO2012121775A2 (en) | 2010-12-21 | 2012-09-13 | Abbott Laboratories | Dual variable domain immunoglobulins and uses thereof |
US8268756B2 (en) | 2004-01-20 | 2012-09-18 | Merus B.V. | Mixture of binding proteins |
EP2500355A2 (en) | 2005-08-19 | 2012-09-19 | Abbott Laboratories | Dual variable domain immunoglobulin and uses thereof |
EP2500037A2 (en) | 2005-05-16 | 2012-09-19 | Abbott Biotechnology Ltd | Use of TNF alpha inhibitor for treatment of erosive polyarthritis |
WO2012125735A1 (en) | 2011-03-15 | 2012-09-20 | Abott Laboratories | An integrated approach to the isolation and purification of antibodies |
WO2012128810A1 (en) | 2011-03-23 | 2012-09-27 | Abbott Laboratories | Methods and systems for the analysis of protein samples |
US8278421B2 (en) | 2006-03-20 | 2012-10-02 | Xoma Techolology Ltd. | Human antibodies specific for gastrin materials and methods |
WO2012134813A1 (en) | 2011-03-31 | 2012-10-04 | St. Jude Children's Research Hospital | Methods and compositions for identifying minimal residual disease in acute lymphoblastic leukemia |
WO2012131053A1 (en) | 2011-03-30 | 2012-10-04 | Ablynx Nv | Methods of treating immune disorders with single domain antibodies against tnf-alpha |
EP2508608A1 (en) | 2003-06-09 | 2012-10-10 | Alnylam Pharmaceuticals Inc. | Method of treating neurodegenerative disease |
WO2012139058A1 (en) | 2011-04-08 | 2012-10-11 | Biogen Idec Ma Inc. | BIOMARKERS PREDICTIVE OF THERAPEUTIC RESPONSIVENESS TO IFNβ AND USES THEREOF |
EP2511301A2 (en) | 2006-08-04 | 2012-10-17 | Medimmune Limited | Human antibodies to ERBB2 |
WO2012142164A1 (en) | 2011-04-12 | 2012-10-18 | The United States Of America, As Represented By The Secretary, Department Of Health & Human Services | Human monoclonal antibodies that bind insulin-like growth factor (igf) i and ii |
US8304451B2 (en) | 2006-05-03 | 2012-11-06 | President And Fellows Of Harvard College | Histone deacetylase and tubulin deacetylase inhibitors |
US8313942B2 (en) | 2008-09-26 | 2012-11-20 | Wyeth Llc | Compatible display vector systems |
EP2526968A2 (en) | 2006-01-27 | 2012-11-28 | Biogen Idec MA Inc. | Nogo receptor antagonists |
US8324350B2 (en) | 2006-12-29 | 2012-12-04 | Abbott Laboratories | Dual-specific IL-1α/IL-1β antibodies |
WO2012167143A1 (en) | 2011-06-03 | 2012-12-06 | Xoma Technology Ltd. | Antibodies specific for tgf-beta |
US8329945B2 (en) | 1996-03-26 | 2012-12-11 | President And Fellows Of Harvard College | Histone deacetylases, and uses related thereto |
EP2535355A2 (en) | 2005-03-23 | 2012-12-19 | Genmab A/S | Antibodies against CD38 for treatment of multiple myeloma |
EP2535425A1 (en) | 2007-05-25 | 2012-12-19 | Decode Genetics EHF. | Variantes génétiques sur les chr 10q26 utilisées comme marqueurs dans l'évaluation, le diagnostic, le pronostic et le traitement d'un risque de cancer du sein |
US8383778B2 (en) | 2009-01-29 | 2013-02-26 | Abbvie Inc. | IL-1 binding proteins |
WO2013028817A1 (en) | 2011-08-23 | 2013-02-28 | Foundation Medicine , Inc. | Novel kif5b-ret fusion molecules and uses thereof |
WO2013040142A2 (en) | 2011-09-16 | 2013-03-21 | Iogenetics, Llc | Bioinformatic processes for determination of peptide binding |
WO2013039996A1 (en) | 2011-09-13 | 2013-03-21 | Dana-Farber Cancer Institute, Inc. | Compositions and methods for brown fat induction and activity using fndc5 |
EP2573563A1 (en) | 2007-12-20 | 2013-03-27 | Heptares Therapeutics Limited | Screening |
US8420083B2 (en) | 2009-10-31 | 2013-04-16 | Abbvie Inc. | Antibodies to receptor for advanced glycation end products (RAGE) and uses thereof |
WO2013054200A2 (en) | 2011-10-10 | 2013-04-18 | The Hospital For Sick Children | Methods and compositions for screening and treating developmental disorders |
WO2013063114A1 (en) | 2011-10-24 | 2013-05-02 | Abbvie Inc. | Immunobinders directed against tnf |
WO2013063095A1 (en) | 2011-10-24 | 2013-05-02 | Abbvie Inc. | Immunobinders directed against sclerostin |
US8435780B2 (en) | 2000-03-03 | 2013-05-07 | President And Fellows Of Harvard College | Class II human histone deacetylases, and uses related thereto |
WO2013067268A1 (en) | 2011-11-03 | 2013-05-10 | Tripath Imaging, Inc. | Methods and compositions for preparing samples for immunostaining |
WO2013067451A2 (en) | 2011-11-04 | 2013-05-10 | Population Diagnostics Inc. | Methods and compositions for diagnosing, prognosing, and treating neurological conditions |
US8440716B2 (en) | 2008-07-23 | 2013-05-14 | President And Fellows Of Harvard College | Deacetylase inhibitors and uses thereof |
WO2013068902A1 (en) | 2011-11-08 | 2013-05-16 | Pfizer Inc. | Methods of treating inflammatory disorders using anti-m-csf antibodies |
WO2013078377A1 (en) | 2011-11-23 | 2013-05-30 | Igenica, Inc. | Anti-cd98 antibodies and methods of use thereof |
WO2013080050A2 (en) | 2011-11-30 | 2013-06-06 | Universitaetsklinikum Erlangen | Methods and compositions for determining responsiveness to treatment with a tnf-alpha inhibitor |
WO2013090633A2 (en) | 2011-12-14 | 2013-06-20 | AbbVie Deutschland GmbH & Co. KG | Composition and method for the diagnosis and treatment of iron-related disorders |
WO2013090635A2 (en) | 2011-12-14 | 2013-06-20 | AbbVie Deutschland GmbH & Co. KG | Composition and method for the diagnosis and treatment of iron-related disorders |
WO2013096516A1 (en) | 2011-12-19 | 2013-06-27 | Xoma Technology Ltd. | Methods for treating acne |
WO2013106485A2 (en) | 2012-01-09 | 2013-07-18 | The Scripps Research Institute | Ultralong complementarity determining regions and uses thereof |
WO2013106489A1 (en) | 2012-01-09 | 2013-07-18 | The Scripps Research Institute | Humanized antibodies with ultralong cdr3s |
WO2013112922A1 (en) | 2012-01-27 | 2013-08-01 | AbbVie Deutschland GmbH & Co. KG | Composition and method for diagnosis and treatment of diseases associated with neurite degeneration |
WO2013119960A2 (en) | 2012-02-08 | 2013-08-15 | Stem Centrx, Inc. | Novel modulators and methods of use |
EP2641618A2 (en) | 2007-07-16 | 2013-09-25 | Genentech, Inc. | Humanized anti-CD79B antibodies and immunoconjugates and methods of use |
WO2013148373A1 (en) | 2012-03-28 | 2013-10-03 | Genentech, Inc. | Anti-hcmv idiotypic antibodies and uses thereof |
US8552154B2 (en) | 2008-09-26 | 2013-10-08 | Emory University | Anti-PD-L1 antibodies and uses therefor |
WO2013151577A1 (en) | 2012-04-02 | 2013-10-10 | Berg Pharma Llc | Interrogatory cell-based assays and uses thereof |
US8557239B2 (en) | 2009-09-14 | 2013-10-15 | Abbvie Inc. | Methods for treating psoriasis using antibodies that bind to the P40 subunit of IL-12 and/or IL-23 |
WO2013158275A1 (en) | 2012-04-20 | 2013-10-24 | Abbvie Inc. | Cell culture methods to reduce acidic species |
WO2013158279A1 (en) | 2012-04-20 | 2013-10-24 | Abbvie Inc. | Protein purification methods to reduce acidic species |
WO2013158273A1 (en) | 2012-04-20 | 2013-10-24 | Abbvie Inc. | Methods to modulate c-terminal lysine variant distribution |
EP2657253A2 (en) | 2008-01-31 | 2013-10-30 | Genentech, Inc. | Anti-CD79b antibodies and immunoconjugates and methods of use |
US8586714B2 (en) | 2009-09-01 | 2013-11-19 | Abbvie, Inc. | Dual variable domain immunoglobulins and uses thereof |
EP2666478A2 (en) | 2006-04-10 | 2013-11-27 | Abbott Biotechnology Ltd | Uses and compositions for treatment of psoriasis |
EP2666480A2 (en) | 2006-04-10 | 2013-11-27 | Abbott Biotechnology Ltd | Uses and compositions for treatment of Crohn's desease |
EP2666472A2 (en) | 2006-04-10 | 2013-11-27 | Abbott Biotechnology Ltd | Uses and compositions for treatment of psoriatic arthritis |
WO2013176754A1 (en) | 2012-05-24 | 2013-11-28 | Abbvie Inc. | Novel purification of antibodies using hydrophobic interaction chromatography |
WO2013177115A2 (en) | 2012-05-21 | 2013-11-28 | Abbvie Inc. | Novel purification of human, humanized, or chimeric antibodies using protein a affinity chromatography |
US8623812B2 (en) | 2004-04-19 | 2014-01-07 | Ohio University | Cross-linkable glycoproteins and methods of making the same |
US8637244B2 (en) | 2006-12-05 | 2014-01-28 | Decode Genetics Ehf. | Genetic markers for risk management of atrial fibrillation, atrial flutter, and stroke |
WO2014043519A1 (en) | 2012-09-14 | 2014-03-20 | Population Diagnostics Inc. | Methods and compositions for diagnosing, prognosing, and treating neurological conditions |
US8697360B2 (en) | 2007-11-30 | 2014-04-15 | Decode Genetics Ehf. | Genetic variants on CHR 11Q and 6Q as markers for prostate and colorectal cancer predisposition |
US8697374B2 (en) | 2008-02-28 | 2014-04-15 | 3M Innovative Properties Company | Antibodies to Clostridium difficile spores and uses thereof |
WO2014058875A2 (en) | 2012-10-09 | 2014-04-17 | Biogen Idec Ma Inc. | Combination therapies and uses for treatment of demyelinating disorders |
WO2014059028A1 (en) | 2012-10-09 | 2014-04-17 | Igenica, Inc. | Anti-c16orf54 antibodies and methods of use thereof |
US8703915B2 (en) | 2009-06-22 | 2014-04-22 | Heptares Therapeutics Limited | Mutant proteins and methods for producing them |
US8716344B2 (en) | 2009-08-11 | 2014-05-06 | President And Fellows Of Harvard College | Class- and isoform-specific HDAC inhibitors and uses thereof |
US8716450B2 (en) | 2009-10-15 | 2014-05-06 | Abbvie Inc. | Dual variable domain immunoglobulins and uses thereof |
WO2014071358A2 (en) | 2012-11-05 | 2014-05-08 | Foundation Medicine, Inc. | Novel ntrk1 fusion molecules and uses thereof |
US8722855B2 (en) | 2009-10-28 | 2014-05-13 | Abbvie Inc. | Dual variable domain immunoglobulins and uses thereof |
WO2014074905A1 (en) | 2012-11-08 | 2014-05-15 | Eleven Biotherapeutics, Inc. | Il-6 antagonists and uses thereof |
WO2014074942A1 (en) | 2012-11-08 | 2014-05-15 | Illumina, Inc. | Risk variants of alzheimer's disease |
US8735546B2 (en) | 2010-08-03 | 2014-05-27 | Abbvie Inc. | Dual variable domain immunoglobulins and uses thereof |
EP2738179A1 (en) | 2006-04-05 | 2014-06-04 | AbbVie Biotechnology Ltd | Antibody purification |
US8748182B2 (en) | 2007-12-08 | 2014-06-10 | Heptares Therapeutics Limited | Mutant proteins and methods for producing them |
WO2014093396A1 (en) | 2012-12-10 | 2014-06-19 | Biogen Idec Ma Inc. | Anti-blood dendritic cell antigen 2 antibodies and uses thereof |
WO2014100542A1 (en) | 2012-12-21 | 2014-06-26 | Abbvie, Inc. | High-throughput antibody humanization |
US8779109B2 (en) | 2010-01-22 | 2014-07-15 | Novo Nordisk Health Care Ag | Growth hormones with prolonged in-vivo efficacy |
US8785135B2 (en) | 2007-03-22 | 2014-07-22 | Heptares Therapeutics Limited | Mutant G-protein coupled receptors and methods for selecting them |
WO2014113729A2 (en) | 2013-01-18 | 2014-07-24 | Foundation Mecicine, Inc. | Methods of treating cholangiocarcinoma |
US8796182B2 (en) | 2009-07-10 | 2014-08-05 | Decode Genetics Ehf. | Genetic markers associated with risk of diabetes mellitus |
US8795963B2 (en) | 2009-04-03 | 2014-08-05 | Decode Genetics Ehf. | Genetic markers for risk management of atrial fibrillation and stroke |
WO2014123696A1 (en) | 2013-01-25 | 2014-08-14 | Thymon, Llc | Compositions for selective reduction of circulating bioactive soluble tnf and methods for treating tnf-mediated disease |
US8809285B2 (en) | 2009-07-31 | 2014-08-19 | Wayne State University | Monophosphorylated lipid A derivatives |
US8808985B2 (en) | 2008-04-01 | 2014-08-19 | Decode Genetics Ehf. | Susceptibility variants for peripheral arterial disease and abdominal aortic aneurysm |
WO2014130879A2 (en) | 2013-02-22 | 2014-08-28 | Stem Centrx, Inc. | Novel antibody conjugates and uses thereof |
US8822645B2 (en) | 2008-07-08 | 2014-09-02 | Abbvie Inc. | Prostaglandin E2 dual variable domain immunoglobulins and uses thereof |
EP2772269A2 (en) | 2009-03-05 | 2014-09-03 | Abbvie Inc. | IL-17 binding proteins |
US8828657B2 (en) | 2008-02-14 | 2014-09-09 | Decode Genetics Ehf. | Susceptibility variants for lung cancer |
WO2014145098A1 (en) | 2013-03-15 | 2014-09-18 | Genentech, Inc. | Cell culture compositions with antioxidants and methods for polypeptide production |
WO2014142882A1 (en) | 2013-03-14 | 2014-09-18 | Abbvie Inc. | Protein purification using displacement chromatography |
WO2014144292A2 (en) | 2013-03-15 | 2014-09-18 | Sanofi Pasteur Biologics , Llc | Antibodies against clostridium difficile toxins and methods of using the same |
WO2014144355A2 (en) | 2013-03-15 | 2014-09-18 | Abbott Laboratories | Anti-gp73 monoclonal antibodies and methods of obtaining the same |
WO2014139994A1 (en) * | 2013-03-11 | 2014-09-18 | Novo Nordisk Health Care Ag | Growth hormone compounds |
US8841249B2 (en) | 2009-08-06 | 2014-09-23 | Novo Nordisk A/S | Growth hormones with prolonged in-vivo efficacy |
WO2014151680A1 (en) | 2013-03-15 | 2014-09-25 | Biogen Idec Ma Inc. | Treatment and prevention of acute kidney injury using anti-alpha v beta 5 antibodies |
WO2014153056A2 (en) | 2013-03-14 | 2014-09-25 | Parkash Gill | Cancer treatment using antibodies that bing cell surface grp78 |
WO2014160497A1 (en) | 2013-03-13 | 2014-10-02 | Genentech, Inc. | Formulations with reduced oxidation |
WO2014160495A1 (en) | 2013-03-13 | 2014-10-02 | Genentech, Inc. | Formulations with reduced oxidation |
WO2014158231A1 (en) | 2013-03-14 | 2014-10-02 | Abbvie Inc. | Low acidic species compositions and methods for producing and using the same |
WO2014159554A1 (en) | 2013-03-14 | 2014-10-02 | Abbvie Inc. | Low acidic species compositions and methods for producing the same using displacement chromatography |
WO2014160490A1 (en) | 2013-03-13 | 2014-10-02 | Genetech, Inc. | Antibody formulations |
US8865868B2 (en) | 2008-08-06 | 2014-10-21 | Novo Nordisk Healthcare Ag | Conjugated proteins with prolonged in vivo efficacy |
US8865400B2 (en) | 2007-02-07 | 2014-10-21 | Decode Genetics Ehf. | Genetic variants contributing to risk of prostate cancer |
US8871468B2 (en) | 1997-07-21 | 2014-10-28 | Ohio University | Synthetic genes for plant gums and other hydroxyproline-rich glycoproteins |
EP2799453A1 (en) | 2009-04-29 | 2014-11-05 | The Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc. | ERG monoclonal antibodies |
US8906864B2 (en) | 2005-09-30 | 2014-12-09 | AbbVie Deutschland GmbH & Co. KG | Binding domains of proteins of the repulsive guidance molecule (RGM) protein family and functional fragments thereof, and their use |
EP2810654A1 (en) | 2008-07-08 | 2014-12-10 | AbbVie Inc. | Prostaglandin E2 binding proteins and uses thereof |
WO2014197885A2 (en) | 2013-06-07 | 2014-12-11 | Duke University | Inhibitors of complement factor h |
US8921279B2 (en) | 2007-06-26 | 2014-12-30 | F-Star Biotechnologische Forschungs—und Entwicklungsges. m.b.H | Display of binding agents |
WO2015010100A2 (en) | 2013-07-18 | 2015-01-22 | Fabrus, Inc. | Humanized antibodies with ultralong complementarity determining regions |
WO2015017529A2 (en) | 2013-07-31 | 2015-02-05 | Dana-Farber Cancer Institute, Inc. | Compositions and methods for modulating thermogenesis using pth-related and egf-related molecules |
WO2015017146A2 (en) | 2013-07-18 | 2015-02-05 | Fabrus, Inc. | Antibodies with ultralong complementarity determining regions |
US8951735B2 (en) | 2008-07-07 | 2015-02-10 | Decode Genetics Ehf. | Genetic variants for breast cancer risk assessment |
US8957187B2 (en) | 2005-12-02 | 2015-02-17 | Genentech, Inc. | Binding polypeptides and uses thereof |
WO2015026846A1 (en) | 2013-08-19 | 2015-02-26 | Biogen Idec Ma Inc. | Control of protein glycosylation by culture medium supplementation and cell culture process parameters |
US8986972B2 (en) | 2012-02-24 | 2015-03-24 | Stem Centrx, Inc. | Nucleic acid encoding DLL3 antibodies |
US8987418B2 (en) | 2013-03-15 | 2015-03-24 | Abbvie Inc. | Dual specific binding proteins directed against IL-1β and/or IL-17 |
EP2851372A1 (en) | 2007-11-30 | 2015-03-25 | Genentech, Inc. | Anti-VEGF antibodies |
WO2015048520A1 (en) | 2013-09-27 | 2015-04-02 | Genentech, Inc. | Anti-pdl1 antibody formulations |
US8999289B2 (en) | 2005-03-22 | 2015-04-07 | President And Fellows Of Harvard College | Treatment of protein degradation disorders |
EP2862867A2 (en) | 2005-10-25 | 2015-04-22 | The Johns Hopkins University | Methods and compositions for the treatment of Marfan syndrome and associated disorders |
WO2015057939A1 (en) | 2013-10-18 | 2015-04-23 | Biogen Idec Ma Inc. | Anti-s1p4 antibodies and uses thereof |
US9017287B2 (en) | 2004-06-23 | 2015-04-28 | Abbvie Biotechnology Ltd | Automatic injection devices |
US9023594B2 (en) | 2008-09-05 | 2015-05-05 | President And Fellows Of Harvard College | Continuous directed evolution of proteins and nucleic acids |
WO2015066190A1 (en) | 2013-10-29 | 2015-05-07 | President And Fellows Of Harvard College | Methods and compositions for inhibting oxidative stress |
US9029508B2 (en) | 2008-04-29 | 2015-05-12 | Abbvie Inc. | Dual variable domain immunoglobulins and uses thereof |
WO2015070068A1 (en) | 2013-11-07 | 2015-05-14 | Abbvie Inc. | Isolation and purification of antibodies |
US9035027B2 (en) | 2008-06-03 | 2015-05-19 | Abbvie Inc. | Dual variable domain immunoglobulins and uses thereof |
WO2015071759A1 (en) | 2013-11-15 | 2015-05-21 | Institut Pasteur | A molecular marker of plasmodium falciparum artemisinin resistance |
US9046513B2 (en) | 2010-08-26 | 2015-06-02 | Abbvie Inc. | Dual variable domain immunoglobulins and uses thereof |
US9045551B2 (en) | 2012-11-01 | 2015-06-02 | Abbvie Inc. | Anti-DLL4/VEGF dual variable domain immunoglobulin and uses thereof |
US9062101B2 (en) | 2010-08-14 | 2015-06-23 | AbbVie Deutschland GmbH & Co. KG | Amyloid-beta binding proteins |
WO2015090230A1 (en) | 2013-12-19 | 2015-06-25 | Novartis Ag | Human mesothelin chimeric antigen receptors and uses thereof |
WO2015095809A1 (en) | 2013-12-20 | 2015-06-25 | Biogen Idec Ma Inc. | Use of perfusion seed cultures to improve biopharmaceutical fed-batch production capacity and product quality |
EP2891722A1 (en) | 2013-11-12 | 2015-07-08 | Population Diagnostics, Inc. | Methods and compositions for diagnosing, prognosing, and treating endometriosis |
US9081020B2 (en) | 2008-02-11 | 2015-07-14 | Heptares Therapeutics Limited | Mutant proteins and methods for selecting them |
WO2015109180A2 (en) | 2014-01-16 | 2015-07-23 | Academia Sinica | Compositions and methods for treatment and detection of cancers |
WO2015120075A2 (en) | 2014-02-04 | 2015-08-13 | Genentech, Inc. | Mutant smoothened and methods of using the same |
WO2015122995A1 (en) | 2014-02-11 | 2015-08-20 | Visterra, Inc. | Antibody moleules to dengue virus and uses thereof |
US9115195B2 (en) | 2010-03-02 | 2015-08-25 | Abbvie Inc. | Therapeutic DLL4 binding proteins |
US9120870B2 (en) | 2011-12-30 | 2015-09-01 | Abbvie Inc. | Dual specific binding proteins directed against IL-13 and IL-17 |
WO2015138920A1 (en) | 2014-03-14 | 2015-09-17 | Novartis Ag | Antibody molecules to lag-3 and uses thereof |
EP2921501A1 (en) | 2008-10-20 | 2015-09-23 | Abbvie Inc. | Isolation and purification of antibodies using Protein A affinity chromatography |
EP2921177A2 (en) | 2010-07-09 | 2015-09-23 | AbbVie Inc. | Dual variable domain immunoglobulins and uses thereof |
US9170262B2 (en) | 2010-06-16 | 2015-10-27 | Abbvie, Inc. | Comparison of protein samples |
WO2015175340A1 (en) | 2014-05-13 | 2015-11-19 | Bavarian Nordic, Inc. | Combination therapy for treating cancer with a poxvirus expressing a tumor antigen and a monoclonal antibody against tim-3 |
WO2015187779A1 (en) | 2014-06-03 | 2015-12-10 | Xbiotech, Inc. | Compositions and methods for treating and preventing staphylococcus aureus infections |
EP2960252A1 (en) | 2014-06-26 | 2015-12-30 | Institut Pasteur | Phospholipase for treatment of immunosuppression |
CN105229035A (en) * | 2013-03-11 | 2016-01-06 | 诺和诺德保健股份有限公司 | Growth hormone compound |
EP2966089A1 (en) | 2011-06-02 | 2016-01-13 | Dyax Corp. | Fc receptor binding proteins |
US9260520B2 (en) | 2008-04-25 | 2016-02-16 | Dyax Corp. | Antibodies to FeRn and uses thereof |
US9259476B2 (en) | 2009-07-31 | 2016-02-16 | Wayne State University | Monophosphorylated lipid A derivatives |
WO2016025880A1 (en) | 2014-08-14 | 2016-02-18 | Novartis Ag | Treatment of cancer using gfr alpha-4 chimeric antigen receptor |
US9266950B2 (en) | 2009-10-20 | 2016-02-23 | Abbvie Inc. | Isolation and purification of anti-IL-13 antibodies using protein a affinity chromatography |
WO2016040880A1 (en) | 2014-09-13 | 2016-03-17 | Novartis Ag | Combination therapies of alk inhibitors |
WO2016042412A1 (en) | 2014-09-16 | 2016-03-24 | Symphogen A/S | Anti-met antibodies and compositions |
WO2016054555A2 (en) | 2014-10-03 | 2016-04-07 | Novartis Ag | Combination therapies |
WO2016061142A1 (en) | 2014-10-14 | 2016-04-21 | Novartis Ag | Antibody molecules to pd-l1 and uses thereof |
WO2016061424A1 (en) | 2014-10-17 | 2016-04-21 | Biogen Ma Inc. | Copper supplementation for control of glycosylation in mammalian cell culture process |
EP3011953A1 (en) | 2008-10-29 | 2016-04-27 | Ablynx N.V. | Stabilised formulations of single domain antigen binding molecules |
WO2016070152A1 (en) | 2014-10-31 | 2016-05-06 | Biogen Ma Inc. | Hypotaurine, gaba, beta-alanine, and choline for control of waste byproduct accumulation in mammalian cell culture process |
WO2016073685A1 (en) | 2014-11-05 | 2016-05-12 | Annexon, Inc. | Humanized anti-complement factor c1q antibodies and uses thereof |
WO2016073894A1 (en) | 2014-11-07 | 2016-05-12 | Eleven Biotherapeutics, Inc. | Therapeutic agents with increased ocular retention |
WO2016081835A2 (en) | 2014-11-21 | 2016-05-26 | University Of Maryland, Baltimore | Targeted structure-specific particulate delivery systems |
WO2016100882A1 (en) | 2014-12-19 | 2016-06-23 | Novartis Ag | Combination therapies |
US9383364B2 (en) | 2011-03-07 | 2016-07-05 | University Of Louisville Research Foundation, Inc. | Predictive marker of DNMT1 inhibitor therapeutic efficacy and methods of using the marker |
US9394537B2 (en) | 2010-12-22 | 2016-07-19 | President And Fellows Of Harvard College | Continuous directed evolution |
WO2016114819A1 (en) | 2015-01-16 | 2016-07-21 | Academia Sinica | Compositions and methods for treatment and detection of cancers |
WO2016118961A1 (en) | 2015-01-24 | 2016-07-28 | Academia Sinica | Cancer markers and methods of use thereof |
WO2016123593A1 (en) | 2015-01-30 | 2016-08-04 | Academia Sinica | Compositions and methods relating to universal glycoforms for enhanced antibody efficacy |
WO2016126972A1 (en) | 2015-02-04 | 2016-08-11 | Genentech, Inc. | Mutant smoothened and methods of using the same |
WO2016141111A1 (en) | 2015-03-03 | 2016-09-09 | Xoma (Us) Llc | Treatment of post-prandial hyperinsulinemia and hypoglycemia after bariatric surgery |
US9441035B2 (en) | 2013-03-15 | 2016-09-13 | Genentech, Inc. | Cell culture media and methods of antibody production |
WO2016144917A1 (en) | 2015-03-10 | 2016-09-15 | University Of Massachusetts | Targeting gdf6 and bmp signaling for anti-melanoma therapy |
WO2016161410A2 (en) | 2015-04-03 | 2016-10-06 | Xoma Technology Ltd. | Treatment of cancer using inhibitors of tgf-beta and pd-1 |
WO2016170022A1 (en) | 2015-04-21 | 2016-10-27 | Institut Gustave Roussy | Therapeutic methods, products and compositions inhibiting znf555 |
US9486584B2 (en) | 2006-06-30 | 2016-11-08 | Abbvie Biotechnology Ltd. | Automatic injection device |
US9499621B2 (en) | 2013-04-08 | 2016-11-22 | Cytodyn, Inc. | Felinized antibodies and methods of treating retroviral infections in felines |
EP3124045A2 (en) | 2006-12-20 | 2017-02-01 | Xoma (Us) Llc | Treatment of il-1 beta related diseases |
WO2017019894A1 (en) | 2015-07-29 | 2017-02-02 | Novartis Ag | Combination therapies comprising antibody molecules to lag-3 |
WO2017019897A1 (en) | 2015-07-29 | 2017-02-02 | Novartis Ag | Combination therapies comprising antibody molecules to tim-3 |
US9561328B2 (en) | 2009-04-29 | 2017-02-07 | Abbvie Biotechnology Ltd | Automatic injection device |
WO2017040342A1 (en) | 2015-08-28 | 2017-03-09 | Genentech, Inc. | Anti-hypusine antibodies and uses thereof |
WO2017049011A1 (en) | 2015-09-15 | 2017-03-23 | Scholar Rock, Inc. | Anti-pro/latent-myostatin antibodies and uses thereof |
US9605069B2 (en) | 2008-02-29 | 2017-03-28 | AbbVie Deutschland GmbH & Co. KG | Antibodies against the RGM a protein and uses thereof |
US9617334B2 (en) | 2012-06-06 | 2017-04-11 | Zoetis Services Llc | Caninized anti-NGF antibodies and methods thereof |
US9617597B2 (en) | 2007-02-21 | 2017-04-11 | Decode Genetics Ehf | Genetic susceptibility variants associated with cardiovascular disease |
WO2017066561A2 (en) | 2015-10-16 | 2017-04-20 | President And Fellows Of Harvard College | Regulatory t cell pd-1 modulation for regulating t cell effector immune responses |
WO2017075329A2 (en) | 2015-10-29 | 2017-05-04 | Dana-Farber Cancer Institute, Inc. | Methods for identification, assessment, prevention, and treatment of metabolic disorders using pm20d1 and n-lipidated amino acids |
WO2017077275A1 (en) * | 2015-11-02 | 2017-05-11 | Imperial Innovations Limited | Phagemid vector |
EP3168232A1 (en) | 2009-11-13 | 2017-05-17 | Dana-Farber Cancer Institute, Inc. | Compositions, kits, and methods for the diagnosis, prognosis, monitoring, treatment and modulation of post-transplant lymphoproliferative disorders and hypoxia associated angiogenesis disorders using galectin-1 |
WO2017083515A2 (en) | 2015-11-10 | 2017-05-18 | Visterra, Inc. | Antibody molecule-drug conjugates and uses thereof |
WO2017091683A1 (en) | 2015-11-25 | 2017-06-01 | Visterra, Inc. | Antibody molecules to april and uses thereof |
US9670276B2 (en) | 2012-07-12 | 2017-06-06 | Abbvie Inc. | IL-1 binding proteins |
WO2017106656A1 (en) | 2015-12-17 | 2017-06-22 | Novartis Ag | Antibody molecules to pd-1 and uses thereof |
WO2017106810A2 (en) | 2015-12-17 | 2017-06-22 | Novartis Ag | Combination of c-met inhibitor with antibody molecule to pd-1 and uses thereof |
WO2017117304A1 (en) | 2015-12-30 | 2017-07-06 | Genentech, Inc. | Use of tryptophan derivatives for protein formulations |
WO2017117311A1 (en) | 2015-12-30 | 2017-07-06 | Genentech, Inc. | Formulations with reduced degradation of polysorbate |
WO2017120523A2 (en) | 2016-01-08 | 2017-07-13 | Scholar Rock, Inc. | Anti-pro/latent myostatin antibodies and methods of use thereof |
EP3199553A1 (en) | 2008-10-29 | 2017-08-02 | China Synthetic Rubber Corporation | Methods and agents for the diagnosis and treatment of hepatocellular carcinoma |
WO2017136558A1 (en) | 2016-02-04 | 2017-08-10 | Curis, Inc. | Mutant smoothened and methods of using the same |
US9737493B2 (en) | 2012-09-07 | 2017-08-22 | University Of Louisville Research Foundation, Inc. | Compositions and methods for modulating DNMT1 inhibitor activity |
US9745375B2 (en) | 2008-07-09 | 2017-08-29 | Biogen Ma Inc. | Compositions comprising antibodies to LINGO or fragments thereof |
US9758805B2 (en) | 2012-04-20 | 2017-09-12 | Merus N.V. | Methods and means for the production of Ig-like molecules |
WO2017156500A1 (en) | 2016-03-11 | 2017-09-14 | Scholar Rock, Inc. | Tgfb1-binding immunoglobulins and use thereof |
WO2017160599A1 (en) | 2016-03-14 | 2017-09-21 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Use of cd300b antagonists to treat sepsis and septic shock |
WO2017158436A1 (en) | 2016-03-17 | 2017-09-21 | Oslo Universitetssykehus Hf | Fusion proteins targeting tumour associated macrophages for treating cancer |
WO2017165464A1 (en) | 2016-03-21 | 2017-09-28 | Elstar Therapeutics, Inc. | Multispecific and multifunctional molecules and uses thereof |
WO2017165736A1 (en) | 2016-03-25 | 2017-09-28 | Visterra, Inc. | Formulation of antibody molecules to dengue virus |
WO2017177199A2 (en) | 2016-04-08 | 2017-10-12 | Iti Health, Inc. | Plectin-1 binding antibodies and uses thereof |
US9790478B2 (en) | 2013-03-14 | 2017-10-17 | Abbott Laboratories | HCV NS3 recombinant antigens and mutants thereof for improved antibody detection |
WO2017181098A2 (en) | 2016-04-15 | 2017-10-19 | Visterra, Inc. | Antibody molecules to zika virus and uses thereof |
US9796780B2 (en) | 2012-05-14 | 2017-10-24 | Biogen Ma Inc. | LINGO-2 antagonists for treatment of conditions involving motor neurons |
US9841427B2 (en) | 2013-03-14 | 2017-12-12 | Abbott Laboratories | HCV antigen-antibody combination assay and methods and compositions for use therein |
US9840554B2 (en) | 2015-06-15 | 2017-12-12 | Abbvie Inc. | Antibodies against platelet-derived growth factor (PDGF) |
US9856311B2 (en) | 2005-01-05 | 2018-01-02 | F-Star Biotechnologische Forschungs- Und Entwicklungsges.M.B.H | Synthetic immunoglobulin domains with binding properties engineered in regions of the molecule different from the complementarity determining regions |
EP3263581A1 (en) | 2005-05-17 | 2018-01-03 | University of Connecticut | Compositions and methods for immunomodulation in an organism |
WO2018005556A1 (en) | 2016-06-27 | 2018-01-04 | Juno Therapeutics, Inc. | Mhc-e restricted epitopes, binding molecules and related methods and uses |
WO2018005559A1 (en) | 2016-06-27 | 2018-01-04 | Juno Therapeutics, Inc. | Method of identifying peptide epitopes, molecules that bind such epitopes and related uses |
WO2018013918A2 (en) | 2016-07-15 | 2018-01-18 | Novartis Ag | Treatment and prevention of cytokine release syndrome using a chimeric antigen receptor in combination with a kinase inhibitor |
WO2018013714A1 (en) | 2016-07-13 | 2018-01-18 | Biogen Ma Inc. | Dosage regimens of lingo-1 antagonists and uses for treatment of demyelinating disorders |
US9879042B2 (en) | 2014-09-08 | 2018-01-30 | Academia Sinica | Human iNKT cell activation using glycolipids |
US9878102B2 (en) | 2011-01-24 | 2018-01-30 | Abbvie Biotechnology Ltd. | Automatic injection devices having overmolded gripping surfaces |
WO2018022479A1 (en) | 2016-07-25 | 2018-02-01 | Biogen Ma Inc. | Anti-hspa5 (grp78) antibodies and uses thereof |
WO2018026748A1 (en) | 2016-08-01 | 2018-02-08 | Xoma (Us) Llc | Parathyroid hormone receptor 1 (pth1r) antibodies and uses thereof |
EP3293275A1 (en) | 2013-06-06 | 2018-03-14 | Dana-Farber Cancer Institute, Inc. | Compositions and methods for identification, assessment prevention, and treatment of cancer using pd-l1 isoforms |
WO2018052556A1 (en) | 2016-08-02 | 2018-03-22 | Visterra, Inc. | Engineered polypeptides and uses thereof |
WO2018057955A1 (en) | 2016-09-23 | 2018-03-29 | Elstar Therapeutics, Inc. | Multispecific antibody molecules comprising lambda and kappa light chains |
WO2018064255A2 (en) | 2016-09-28 | 2018-04-05 | Xoma (Us) Llc | Antibodies that bind interleukin-2 and uses thereof |
WO2018067474A1 (en) | 2016-10-03 | 2018-04-12 | Abbott Laboratories | Improved methods of assessing gfap status in patient samples |
WO2018067992A1 (en) | 2016-10-07 | 2018-04-12 | Novartis Ag | Chimeric antigen receptors for the treatment of cancer |
WO2018071576A1 (en) | 2016-10-14 | 2018-04-19 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Treatment of tumors by inhibition of cd300f |
US9951125B2 (en) | 2006-11-30 | 2018-04-24 | Abbvie Inc. | Aβ conformer selective anti-Aβ globulomer monoclonal antibodies |
US9957506B2 (en) | 2013-09-25 | 2018-05-01 | Cornell University | Compounds for inducing anti-tumor immunity and methods thereof |
US9956236B2 (en) | 2011-02-07 | 2018-05-01 | Cornell University | Methods for increasing immune responses using agents that directly bind to and activate IRE-1 |
US9975965B2 (en) | 2015-01-16 | 2018-05-22 | Academia Sinica | Compositions and methods for treatment and detection of cancers |
US9981030B2 (en) | 2013-06-27 | 2018-05-29 | Academia Sinica | Glycan conjugates and use thereof |
EP3335728A1 (en) | 2008-10-10 | 2018-06-20 | Children's Medical Center Corporation | Biochemically stabilized hiv-1 env trimer vaccine |
US10005847B2 (en) | 2014-05-27 | 2018-06-26 | Academia Sinica | Anti-HER2 glycoantibodies and uses thereof |
EP3339445A1 (en) | 2006-09-08 | 2018-06-27 | AbbVie Bahamas Ltd. | Interleukin -13 binding proteins |
EP3338793A1 (en) | 2013-08-28 | 2018-06-27 | AbbVie Stemcentrx LLC | Novel sez6 modulators and methods of use |
WO2018119402A1 (en) | 2016-12-23 | 2018-06-28 | Visterra, Inc. | Binding polypeptides and methods of making the same |
WO2018129395A1 (en) | 2017-01-06 | 2018-07-12 | Scholar Rock, Inc. | Methods for treating metabolic diseases by inhibiting myostatin activation |
WO2018129329A1 (en) | 2017-01-06 | 2018-07-12 | Scholar Rock, Inc. | ISOFORM-SPECIFIC, CONTEXT-PERMISSIVE TGFβ1 INHIBITORS AND USE THEREOF |
US10023892B2 (en) | 2014-05-27 | 2018-07-17 | Academia Sinica | Compositions and methods relating to universal glycoforms for enhanced antibody efficacy |
WO2018130660A1 (en) | 2017-01-13 | 2018-07-19 | Academia Sinica | Reloadable hydrogel system for treating myocardial infarction |
WO2018130661A1 (en) | 2017-01-13 | 2018-07-19 | Academia Sinica | Reloadable hydrogel system for treating brain conditions |
WO2018136626A1 (en) | 2017-01-18 | 2018-07-26 | Visterra, Inc. | Antibody molecule-drug conjugates and uses thereof |
WO2018136553A1 (en) | 2017-01-18 | 2018-07-26 | Genentech, Inc. | Idiotypic antibodies against anti-pd-l1 antibodies and uses thereof |
US10035853B2 (en) | 2013-08-28 | 2018-07-31 | Abbvie Stemcentrx Llc | Site-specific antibody conjugation methods and compositions |
WO2018151820A1 (en) | 2017-02-16 | 2018-08-23 | Elstar Therapeutics, Inc. | Multifunctional molecules comprising a trimeric ligand and uses thereof |
US10059997B2 (en) | 2010-08-02 | 2018-08-28 | Population Bio, Inc. | Compositions and methods for discovery of causative mutations in genetic disorders |
WO2018158719A1 (en) | 2017-03-02 | 2018-09-07 | Novartis Ag | Engineered heterodimeric proteins |
WO2018175942A1 (en) | 2017-03-23 | 2018-09-27 | Abbott Laboratories | Methods for aiding in the diagnosis and determination of the extent of traumatic brain injury in a human subject using the early biomarker ubiquitin carboxy-terminal hydrolase l1 |
WO2018176019A1 (en) | 2017-03-24 | 2018-09-27 | The Regents Of The University Of California | Proteoglycan irregularities in abnormal fibroblasts and therapies based therefrom |
US10087236B2 (en) | 2009-12-02 | 2018-10-02 | Academia Sinica | Methods for modifying human antibodies by glycan engineering |
US10086054B2 (en) | 2013-06-26 | 2018-10-02 | Academia Sinica | RM2 antigens and use thereof |
US10093733B2 (en) | 2014-12-11 | 2018-10-09 | Abbvie Inc. | LRP-8 binding dual variable domain immunoglobulin proteins |
WO2018187227A1 (en) | 2017-04-03 | 2018-10-11 | Concologie, Inc. | Methods for treating cancer using ps-targeting antibodies with immuno-oncology agents |
WO2018189611A1 (en) | 2017-04-12 | 2018-10-18 | Pfizer Inc. | Antibodies having conditional affinity and methods of use thereof |
WO2018191531A1 (en) | 2017-04-15 | 2018-10-18 | Abbott Laboratories | Methods for aiding in the hyperacute diagnosis and determination of traumatic brain injury in a human subject using early biomarkers |
WO2018195283A1 (en) | 2017-04-19 | 2018-10-25 | Elstar Therapeutics, Inc. | Multispecific molecules and uses thereof |
US10111951B2 (en) | 2013-09-06 | 2018-10-30 | Academia Sinica | Human iNKT cell activation using glycolipids with altered glycosyl groups |
WO2018197859A1 (en) * | 2017-04-24 | 2018-11-01 | Imperial Innovations Limited | Cancer treatment |
WO2018201047A1 (en) | 2017-04-28 | 2018-11-01 | Elstar Therapeutics, Inc. | Multispecific molecules comprising a non-immunoglobulin heterodimerization domain and uses thereof |
WO2018200823A1 (en) | 2017-04-28 | 2018-11-01 | Abbott Laboratories | Methods for aiding in the hyperacute diagnosis and determination of traumatic brain injury using early biomarkers on at least two samples from the same human subject |
US10119972B2 (en) | 2014-03-27 | 2018-11-06 | Academia Sinica | Reactive labelling compounds and uses thereof |
US10118962B2 (en) | 2008-10-29 | 2018-11-06 | Ablynx N.V. | Methods for purification of single domain antigen binding molecules |
US10118969B2 (en) | 2014-05-27 | 2018-11-06 | Academia Sinica | Compositions and methods relating to universal glycoforms for enhanced antibody efficacy |
US10130714B2 (en) | 2012-04-14 | 2018-11-20 | Academia Sinica | Enhanced anti-influenza agents conjugated with anti-inflammatory activity |
WO2018218169A1 (en) | 2017-05-25 | 2018-11-29 | Abbott Laboratories | Methods for aiding in the determination of whether to perform imaging on a human subject who has sustained or may have sustained an injury to the head using early biomarkers |
WO2018215535A1 (en) | 2017-05-23 | 2018-11-29 | Helmholtz Zentrum München - Deutsches Forschungszentrum für Gesundheit und Umwelt (GmbH) | Novel cd73 antibody, preparation and uses thereof |
WO2018222783A1 (en) | 2017-05-30 | 2018-12-06 | Abbott Laboratories | Methods for aiding in diagnosing and evaluating a mild traumatic brain injury in a human subject using cardiac troponin i and early biomarkers |
WO2018222901A1 (en) | 2017-05-31 | 2018-12-06 | Elstar Therapeutics, Inc. | Multispecific molecules that bind to myeloproliferative leukemia (mpl) protein and uses thereof |
US10150818B2 (en) | 2014-01-16 | 2018-12-11 | Academia Sinica | Compositions and methods for treatment and detection of cancers |
WO2018226336A1 (en) | 2017-06-09 | 2018-12-13 | Providence Health & Services - Oregon | Utilization of cd39 and cd103 for identification of human tumor reactive cells for treatment of cancer |
WO2018237173A1 (en) | 2017-06-22 | 2018-12-27 | Novartis Ag | Antibody molecules to cd73 and uses thereof |
WO2019006007A1 (en) | 2017-06-27 | 2019-01-03 | Novartis Ag | Dosage regimens for anti-tim-3 antibodies and uses thereof |
WO2019010131A1 (en) | 2017-07-03 | 2019-01-10 | Abbott Laboratories | Improved methods for measuring ubiquitin carboxy-terminal hydrolase l1 levels in blood |
US10179911B2 (en) | 2014-01-20 | 2019-01-15 | President And Fellows Of Harvard College | Negative selection and stringency modulation in continuous evolution systems |
WO2019014572A1 (en) | 2017-07-14 | 2019-01-17 | Pfizer, Inc. | Antibodies to madcam |
EP3431496A1 (en) | 2017-07-19 | 2019-01-23 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Anti- isoasp7 amyloid beta antibodies and uses thereof |
WO2019018730A1 (en) | 2017-07-20 | 2019-01-24 | Novartis Ag | Dosage regimens of anti-lag-3 antibodies and uses thereof |
WO2019023661A1 (en) | 2017-07-28 | 2019-01-31 | Scholar Rock, Inc. | Ltbp complex-specific inhibitors of tgf-beta 1 and uses thereof |
US10197573B2 (en) | 2013-03-14 | 2019-02-05 | Abbott Laboratories | HCV core lipid binding domain monoclonal antibodies |
US10210306B2 (en) | 2006-05-03 | 2019-02-19 | Population Bio, Inc. | Evaluating genetic disorders |
US10208120B2 (en) | 2014-11-05 | 2019-02-19 | Genentech, Inc. | Anti-FGFR2/3 antibodies and methods using same |
US10208109B2 (en) | 2005-11-30 | 2019-02-19 | Abbvie Inc. | Monoclonal antibodies against amyloid beta protein and uses thereof |
WO2019035938A1 (en) | 2017-08-16 | 2019-02-21 | Elstar Therapeutics, Inc. | Multispecific molecules that bind to bcma and uses thereof |
US10214765B2 (en) | 2012-08-18 | 2019-02-26 | Academia Sinica | Cell-permeable probes for identification and imaging of sialidases |
US10233495B2 (en) | 2012-09-27 | 2019-03-19 | The Hospital For Sick Children | Methods and compositions for screening and treating developmental disorders |
US10240205B2 (en) | 2017-02-03 | 2019-03-26 | Population Bio, Inc. | Methods for assessing risk of developing a viral disease using a genetic test |
EP3461841A1 (en) | 2017-10-02 | 2019-04-03 | Certest Biotec, S.L. | Antibodies and test devices for the detection of bacteria of the genus campylobacter |
US10253101B2 (en) | 2015-08-06 | 2019-04-09 | Xoma (Us) Llc | Antibody fragments against the insulin receptor and uses thereof to treat hypoglycemia |
WO2019070161A2 (en) | 2017-10-04 | 2019-04-11 | Opko Pharmaceuticals, Llc | Articles and methods directed to personalized therapy of cancer |
WO2019070726A1 (en) | 2017-10-02 | 2019-04-11 | Visterra, Inc. | Antibody molecules to cd138 and uses thereof |
WO2019077165A1 (en) | 2017-10-20 | 2019-04-25 | Institut Curie | Dap10/12 based cars adapted for rush |
WO2019077132A1 (en) | 2017-10-19 | 2019-04-25 | Debiopharm International S.A. | Combination product for the treatment of cancer |
US10274488B2 (en) | 2008-07-15 | 2019-04-30 | Academia Sinica | Glycan arrays on PTFE-like aluminum coated glass slides and related methods |
WO2019099838A1 (en) | 2017-11-16 | 2019-05-23 | Novartis Ag | Combination therapies |
US10308721B2 (en) | 2014-02-21 | 2019-06-04 | Abbvie Stemcentrx Llc | Anti-DLL3 antibodies and drug conjugates for use in melanoma |
WO2019108755A1 (en) | 2017-11-30 | 2019-06-06 | Genentech, Inc. | Anti-pd-l1 antibodies and methods of using the same for detection of pd-l1 |
US10317393B2 (en) | 2007-03-23 | 2019-06-11 | Academia Sinica | Alkynyl sugar analogs for labeling and visualization of glycoconjugates in cells |
WO2019112860A1 (en) | 2017-12-09 | 2019-06-13 | Abbott Laboratories | Methods for aiding in diagnosing and evaluating a traumatic brain injury in a human subject using a combination of gfap and uch-l1 |
WO2019113464A1 (en) | 2017-12-08 | 2019-06-13 | Elstar Therapeutics, Inc. | Multispecific molecules and uses thereof |
WO2019113525A2 (en) | 2017-12-09 | 2019-06-13 | Abbott Laboratories | Methods for aiding in the diagnosis and evaluation of a subject who has sustained an orthopedic injury and that has or may have sustained an injury to the head, such as mild traumatic brain injury (tbi), using glial fibrillary acidic protein (gfap) and/or ubiquitin carboxy-terminal hydrolase l1 (uch-l1) |
US10338069B2 (en) | 2010-04-12 | 2019-07-02 | Academia Sinica | Glycan arrays for high throughput screening of viruses |
US10336784B2 (en) | 2016-03-08 | 2019-07-02 | Academia Sinica | Methods for modular synthesis of N-glycans and arrays thereof |
US10342858B2 (en) | 2015-01-24 | 2019-07-09 | Academia Sinica | Glycan conjugates and methods of use thereof |
EP3511413A1 (en) | 2014-07-25 | 2019-07-17 | Theravectys | Lentiviral vectors for regulated expression of a chimeric antigen receptor molecule |
EP3514179A1 (en) | 2014-01-24 | 2019-07-24 | Dana-Farber Cancer Institute, Inc. | Antibody molecules to pd-1 and uses thereof |
WO2019152810A1 (en) | 2018-02-02 | 2019-08-08 | Bio-Techne Corporation | Compounds that modulate the interaction of vista and vsig3 and methods of making and using |
US10392674B2 (en) | 2015-07-22 | 2019-08-27 | President And Fellows Of Harvard College | Evolution of site-specific recombinases |
US10400037B2 (en) | 2014-09-30 | 2019-09-03 | Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts | Binding molecules, especially antibodies, binding to L1CAM (CD171) |
US10407724B2 (en) | 2012-02-09 | 2019-09-10 | The Hospital For Sick Children | Methods and compositions for screening and treating developmental disorders |
WO2019178364A2 (en) | 2018-03-14 | 2019-09-19 | Elstar Therapeutics, Inc. | Multifunctional molecules and uses thereof |
WO2019178362A1 (en) | 2018-03-14 | 2019-09-19 | Elstar Therapeutics, Inc. | Multifunctional molecules that bind to calreticulin and uses thereof |
WO2019180272A1 (en) | 2018-03-23 | 2019-09-26 | Fundación Instituto De Investigación Sanitaria De Santiago De Compostela | Anti-leptin affinity reagents for use in the treatment of obesity and other leptin-resistance associated diseases |
US10428145B2 (en) | 2015-09-29 | 2019-10-01 | Celgene Corporation | PD-1 binding proteins and methods of use thereof |
WO2019185515A1 (en) | 2018-03-26 | 2019-10-03 | Glycanostics S.R.O. | Means and methods for glycoprofiling of a protein |
US10435467B2 (en) | 2015-01-08 | 2019-10-08 | Biogen Ma Inc. | LINGO-1 antagonists and uses for treatment of demyelinating disorders |
WO2019200229A1 (en) | 2018-04-13 | 2019-10-17 | Novartis Ag | Dosage regimens for anti-pd-l1 antibodies and uses thereof |
EP3569245A1 (en) | 2006-09-26 | 2019-11-20 | Genmab A/S | Combination treatment of cd38-expressing tumors |
US10495645B2 (en) | 2015-01-16 | 2019-12-03 | Academia Sinica | Cancer markers and methods of use thereof |
EP3574919A1 (en) | 2011-07-13 | 2019-12-04 | AbbVie Inc. | Methods and compositions for treating asthma using anti-il-13 antibodies |
WO2019229658A1 (en) | 2018-05-30 | 2019-12-05 | Novartis Ag | Entpd2 antibodies, combination therapies, and methods of using the antibodies and combination therapies |
USRE47770E1 (en) | 2002-07-18 | 2019-12-17 | Merus N.V. | Recombinant production of mixtures of antibodies |
WO2019246293A2 (en) | 2018-06-19 | 2019-12-26 | Atarga, Llc | Antibody molecules to complement component 5 and uses thereof |
US10522240B2 (en) | 2006-05-03 | 2019-12-31 | Population Bio, Inc. | Evaluating genetic disorders |
WO2020008083A1 (en) | 2018-07-05 | 2020-01-09 | Consejo Superior De Investigaciones Científicas | Therapeutic target in chemokine receptors for the screening of compounds useful for the treatment of pathological processes involving chemokine signaling |
WO2020010250A2 (en) | 2018-07-03 | 2020-01-09 | Elstar Therapeutics, Inc. | Anti-tcr antibody molecules and uses thereof |
WO2020014460A1 (en) | 2018-07-11 | 2020-01-16 | Scholar Rock, Inc. | HIGH-AFFINITY, ISOFORM-SELECTIVE TGFβ1 INHIBITORS AND USE THEREOF |
WO2020014473A1 (en) | 2018-07-11 | 2020-01-16 | Scholar Rock, Inc. | TGFβ1 INHIBITORS AND USE THEREOF |
US10538592B2 (en) | 2016-08-22 | 2020-01-21 | Cho Pharma, Inc. | Antibodies, binding fragments, and methods of use |
WO2020021465A1 (en) | 2018-07-25 | 2020-01-30 | Advanced Accelerator Applications (Italy) S.R.L. | Method of treatment of neuroendocrine tumors |
WO2020033485A1 (en) | 2018-08-08 | 2020-02-13 | Genentech, Inc. | Use of tryptophan derivatives and l-methionine for protein formulation |
EP3613765A1 (en) | 2012-08-03 | 2020-02-26 | Dana-Farber Cancer Institute, Inc. | Antibody against repulsive guidance molecule b (rgmb) |
EP3626744A1 (en) | 2015-05-29 | 2020-03-25 | AbbVie Inc. | Anti-cd40 antibodies and uses thereof |
WO2020065594A1 (en) | 2018-09-28 | 2020-04-02 | Kyowa Kirin Co., Ltd. | Il-36 antibodies and uses thereof |
WO2020069372A1 (en) | 2018-09-27 | 2020-04-02 | Elstar Therapeutics, Inc. | Csf1r/ccr2 multispecific antibodies |
US10611794B2 (en) | 2013-09-25 | 2020-04-07 | Bioverativ Therapeutics Inc. | On-column viral inactivation methods |
US10612011B2 (en) | 2015-07-30 | 2020-04-07 | President And Fellows Of Harvard College | Evolution of TALENs |
EP3632931A1 (en) | 2014-11-07 | 2020-04-08 | Sesen Bio, Inc. | Improved il-6 antibodies |
WO2020070303A1 (en) | 2018-10-05 | 2020-04-09 | Bavarian Nordic A/S | Combination therapy for treating cancer with an intravenous administration of a recombinant mva and an immune checkpoint antagonist or agonist |
WO2020079580A1 (en) | 2018-10-15 | 2020-04-23 | Novartis Ag | Trem2 stabilizing antibodies |
WO2020086408A1 (en) | 2018-10-26 | 2020-04-30 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | A high-yield perfusion-based transient gene expression bioprocess |
WO2020086736A1 (en) | 2018-10-23 | 2020-04-30 | Scholar Rock, Inc. | Rgmc-selective inhibitors and use thereof |
US10653779B2 (en) | 2013-03-13 | 2020-05-19 | Genentech, Inc. | Formulations with reduced oxidation |
WO2020104531A1 (en) | 2018-11-20 | 2020-05-28 | Bavarian Nordic A/S | Therapy for treating cancer with an intratumoral and/or intravenous administration of a recombinant mva encoding 4-1bbl (cd137l) and/or cd40l |
WO2020128898A1 (en) | 2018-12-20 | 2020-06-25 | Novartis Ag | Pharmaceutical combinations |
WO2020128927A1 (en) | 2018-12-20 | 2020-06-25 | Kyowa Kirin Co., Ltd. | Fn14 antibodies and uses thereof |
EP3677278A1 (en) | 2018-07-11 | 2020-07-08 | Scholar Rock, Inc. | Isoform selective tgfbeta1 inhibitors and use thereof |
US10717965B2 (en) | 2013-01-10 | 2020-07-21 | Gloriana Therapeutics, Inc. | Mammalian cell culture-produced neublastin antibodies |
US10724096B2 (en) | 2014-09-05 | 2020-07-28 | Population Bio, Inc. | Methods and compositions for inhibiting and treating neurological conditions |
EP3689905A2 (en) | 2019-01-30 | 2020-08-05 | Scholar Rock, Inc. | Ltbp complex-specific inhibitors of tgf-beta and uses thereof |
EP3693063A1 (en) | 2019-02-06 | 2020-08-12 | Diaccurate | Methods and compositions for treating cancer |
EP3696191A1 (en) | 2019-02-14 | 2020-08-19 | Fundación Instituto de Investigación contra la Leucemia Josep Carreras (IJC) | Car t-cells for the treatment of cd1a-positive cancer |
WO2020165868A1 (en) | 2019-02-15 | 2020-08-20 | Perkinelmer Cellular Technologies Germany Gmbh | Low-power microscope-objective pre-scan and high-power microscope-objective scan in x,y and z-direction for imaging objects such as cells using a microscope |
US10751414B2 (en) | 2016-09-19 | 2020-08-25 | Celgene Corporation | Methods of treating psoriasis using PD-1 binding antibodies |
US10752689B2 (en) | 2017-06-26 | 2020-08-25 | Bio-Techne Corporation | Hybridoma clones, monoclonal antibodies to VSIG-4, and methods of making and using |
WO2020172596A1 (en) | 2019-02-21 | 2020-08-27 | Elstar Therapeutics, Inc. | Anti-tcr antibody molecules and thereof |
WO2020172601A1 (en) | 2019-02-21 | 2020-08-27 | Elstar Therapeutics, Inc. | Multifunctional molecules that bind to calreticulin and uses thereof |
WO2020172598A1 (en) | 2019-02-21 | 2020-08-27 | Elstar Therapeutics, Inc. | Multifunctional molecules that bind to t cells and uses thereof to treat autoimmune disorders |
WO2020172605A1 (en) | 2019-02-21 | 2020-08-27 | Elstar Therapeutics, Inc. | Antibody molecules that bind to nkp30 and uses thereof |
WO2020172571A1 (en) | 2019-02-21 | 2020-08-27 | Elstar Therapeutics, Inc. | Multifunctional molecules that bind to t cell related cancer cells and uses thereof |
US10766958B2 (en) | 2016-09-19 | 2020-09-08 | Celgene Corporation | Methods of treating vitiligo using PD-1 binding antibodies |
EP3712171A1 (en) | 2014-08-19 | 2020-09-23 | Novartis AG | Treatment of cancer using a cd123 chimeric antigen receptor |
WO2020205523A1 (en) | 2019-03-29 | 2020-10-08 | Atarga, Llc | Anti fgf23 antibody |
EP3722316A1 (en) | 2014-07-21 | 2020-10-14 | Novartis AG | Treatment of cancer using a cd33 chimeric antigen receptor |
WO2020213724A1 (en) | 2019-04-19 | 2020-10-22 | 中外製薬株式会社 | Chimeric receptor recognizing modification site of antibody |
EP3738981A1 (en) | 2014-01-24 | 2020-11-18 | NGM Biopharmaceuticals, Inc. | Antibodies binding beta klotho domain 2 and methods of use thereof |
US10865238B1 (en) | 2017-05-05 | 2020-12-15 | Duke University | Complement factor H antibodies |
WO2020257289A2 (en) | 2019-06-17 | 2020-12-24 | Visterra, Inc. | Humanized antibody molecules to cd138 and uses thereof |
EP3757130A1 (en) | 2013-09-26 | 2020-12-30 | Costim Pharmaceuticals Inc. | Methods for treating hematologic cancers |
WO2021010326A1 (en) | 2019-07-12 | 2021-01-21 | 中外製薬株式会社 | Anti-mutation type fgfr3 antibody and use therefor |
WO2021021606A1 (en) | 2019-07-26 | 2021-02-04 | Visterra, Inc. | Interleukin-2 agents and uses thereof |
WO2021023860A1 (en) | 2019-08-07 | 2021-02-11 | Db Biotech, As | Improved horseradish peroxidase polypeptides |
WO2021023721A1 (en) | 2019-08-02 | 2021-02-11 | Fundacio Clinic Per A La Recerca Biomedica | Car t-cells against bcma for the treatment of multiple myeloma |
US10920208B2 (en) | 2014-10-22 | 2021-02-16 | President And Fellows Of Harvard College | Evolution of proteases |
US10927342B2 (en) | 2015-08-04 | 2021-02-23 | Regeneran Pharmaceuticals, Inc. | Taurine supplemented cell culture medium and methods of use |
US10935544B2 (en) | 2015-09-04 | 2021-03-02 | Obi Pharma, Inc. | Glycan arrays and method of use |
WO2021044009A1 (en) | 2019-09-04 | 2021-03-11 | Deutsches Zentrum Für Neurodegenerative Erkrankungen E.V. (Dzne) | Herv inhibitors for use in treating tauopathies |
WO2021053559A1 (en) | 2019-09-18 | 2021-03-25 | Novartis Ag | Entpd2 antibodies, combination therapies, and methods of using the antibodies and combination therapies |
WO2021053560A1 (en) | 2019-09-18 | 2021-03-25 | Novartis Ag | Combination therapy with entpd2 and cd73 antibodies |
US10961585B2 (en) | 2018-08-08 | 2021-03-30 | Pml Screening, Llc | Methods for assessing risk of developing a viral of disease using a genetic test |
US10980894B2 (en) | 2016-03-29 | 2021-04-20 | Obi Pharma, Inc. | Antibodies, pharmaceutical compositions and methods |
US10982002B2 (en) | 2018-03-12 | 2021-04-20 | Zoetis Services Llc | Anti-NGF antibodies and methods thereof |
WO2021079188A1 (en) | 2019-10-21 | 2021-04-29 | Novartis Ag | Combination therapies with venetoclax and tim-3 inhibitors |
WO2021079195A1 (en) | 2019-10-21 | 2021-04-29 | Novartis Ag | Tim-3 inhibitors and uses thereof |
US11000601B2 (en) | 2016-11-21 | 2021-05-11 | Obi Pharma, Inc. | Conjugated biological molecules, pharmaceutical compositions and methods |
WO2021099586A1 (en) | 2019-11-20 | 2021-05-27 | Bavarian Nordic A/S | Recombinant mva viruses for intratumoral and/or intravenous administration for treating cancer |
US11041017B2 (en) | 2016-03-29 | 2021-06-22 | Obi Pharma, Inc. | Antibodies, pharmaceutical compositions and methods |
WO2021123902A1 (en) | 2019-12-20 | 2021-06-24 | Novartis Ag | Combination of anti tim-3 antibody mbg453 and anti tgf-beta antibody nis793, with or without decitabine or the anti pd-1 antibody spartalizumab, for treating myelofibrosis and myelodysplastic syndrome |
US11045523B2 (en) | 2013-04-05 | 2021-06-29 | Novo Nordisk Healthcare Ag | Formulation of growth hormone albumin-binder conjugate |
WO2021138407A2 (en) | 2020-01-03 | 2021-07-08 | Marengo Therapeutics, Inc. | Multifunctional molecules that bind to cd33 and uses thereof |
WO2021142427A1 (en) | 2020-01-11 | 2021-07-15 | Scholar Rock, Inc. | TGFβ INHIBITORS AND USE THEREOF |
WO2021142448A2 (en) | 2020-01-11 | 2021-07-15 | Scholar Rock,Inc. | Tgf-beta inhibitors and use thereof |
WO2021144657A1 (en) | 2020-01-17 | 2021-07-22 | Novartis Ag | Combination comprising a tim-3 inhibitor and a hypomethylating agent for use in treating myelodysplastic syndrome or chronic myelomonocytic leukemia |
WO2021146320A1 (en) | 2020-01-13 | 2021-07-22 | Visterra, Inc. | Antibody molecules to c5ar1 and uses thereof |
WO2021159024A1 (en) | 2020-02-05 | 2021-08-12 | Larimar Therapeutics, Inc. | Tat peptide binding proteins and uses thereof |
WO2021180890A1 (en) | 2020-03-11 | 2021-09-16 | Fundació Institut De Recerca Contra La Leucèmia Josep Carreras | Cd22 targeting-moiety for the treatment of b-cell acute lymphoblastic leukemia (b-all) |
US11124760B2 (en) | 2014-03-24 | 2021-09-21 | Biogen Ma Inc. | Methods for overcoming glutamine deprivation during mammalian cell culture |
WO2021203024A1 (en) | 2020-04-03 | 2021-10-07 | Visterra, Inc. | Antibody molecule-drug conjugates and uses thereof |
WO2021211331A1 (en) | 2020-04-13 | 2021-10-21 | Abbott Point Of Care Inc. | METHODS, COMPLEXES AND KITS FOR DETECTING OR DETERMINING AN AMOUNT OF A ß-CORONAVIRUS ANTIBODY IN A SAMPLE |
WO2021217085A1 (en) | 2020-04-24 | 2021-10-28 | Marengo Therapeutics, Inc. | Multifunctional molecules that bind to t cell related cancer cells and uses thereof |
WO2021220218A1 (en) | 2020-05-01 | 2021-11-04 | Novartis Ag | Immunoglobulin variants |
WO2021220215A1 (en) | 2020-05-01 | 2021-11-04 | Novartis Ag | Engineered immunoglobulins |
WO2021222333A1 (en) | 2020-04-30 | 2021-11-04 | Genentech, Inc. | Kras specific antibodies and uses thereof |
WO2021239666A1 (en) | 2020-05-26 | 2021-12-02 | Diaccurate | Therapeutic methods |
WO2021247908A1 (en) | 2020-06-03 | 2021-12-09 | Bionecure Therapeutics, Inc. | Trophoblast cell-surface antigen-2 (trop-2) antibodies |
US11203645B2 (en) | 2018-06-27 | 2021-12-21 | Obi Pharma, Inc. | Glycosynthase variants for glycoprotein engineering and methods of use |
US11208452B2 (en) | 2015-06-02 | 2021-12-28 | Novo Nordisk A/S | Insulins with polar recombinant extensions |
WO2021262999A1 (en) | 2020-06-24 | 2021-12-30 | Visterra, Inc. | Antibody molecules to april and uses thereof |
WO2022010797A2 (en) | 2020-07-07 | 2022-01-13 | Bionecure Therapeutics, Inc. | Novel maytansinoids as adc payloads and their use for the treatment of cancer |
US11237165B2 (en) | 2008-06-27 | 2022-02-01 | Merus N.V. | Antibody producing non-human animals |
WO2022026592A2 (en) | 2020-07-28 | 2022-02-03 | Celltas Bio, Inc. | Antibody molecules to coronavirus and uses thereof |
WO2022031804A1 (en) | 2020-08-04 | 2022-02-10 | Abbott Laboratories | Improved methods and kits for detecting sars-cov-2 protein in a sample |
WO2022046920A2 (en) | 2020-08-26 | 2022-03-03 | Marengo Therapeutics, Inc. | Multifunctional molecules that bind to calreticulin and uses thereof |
WO2022043558A1 (en) | 2020-08-31 | 2022-03-03 | Advanced Accelerator Applications International Sa | Method of treating psma-expressing cancers |
WO2022046922A2 (en) | 2020-08-26 | 2022-03-03 | Marengo Therapeutics, Inc. | Antibody molecules that bind to nkp30 and uses thereof |
WO2022043557A1 (en) | 2020-08-31 | 2022-03-03 | Advanced Accelerator Applications International Sa | Method of treating psma-expressing cancers |
WO2022047046A1 (en) | 2020-08-26 | 2022-03-03 | Marengo Therapeutics, Inc. | Methods of detecting trbc1 or trbc2 |
US11292825B2 (en) | 2015-10-01 | 2022-04-05 | Novo Nordisk A/S | Protein conjugates |
US11299729B2 (en) | 2015-04-17 | 2022-04-12 | President And Fellows Of Harvard College | Vector-based mutagenesis system |
WO2022081718A1 (en) | 2020-10-14 | 2022-04-21 | Five Prime Therapeutics, Inc. | Anti-c-c chemokine receptor 8 (ccr8) antibodies and methods of use thereof |
US11332523B2 (en) | 2014-05-28 | 2022-05-17 | Academia Sinica | Anti-TNF-alpha glycoantibodies and uses thereof |
WO2022115538A1 (en) | 2020-11-24 | 2022-06-02 | Bio-Techne Corporation | Anti-severe acute respiratory syndrome coronavirus antibodies |
WO2022119841A1 (en) | 2020-12-01 | 2022-06-09 | Abbott Laboratories | Use of one or more biomarkers to determine traumatic brain injury (tbi) in a subject having received a head computerized tomography scan that is negative for a tbi |
WO2022120224A1 (en) | 2020-12-04 | 2022-06-09 | Visterra, Inc. | Methods of using interleukin-2 agents |
WO2022133191A2 (en) | 2020-12-18 | 2022-06-23 | Kiniksa Pharmaceuticals, Ltd. | Protein compositions and methods for producing and using the same |
US11370833B2 (en) | 2014-09-15 | 2022-06-28 | Genentech, Inc. | Antibody formulations |
US11377485B2 (en) | 2009-12-02 | 2022-07-05 | Academia Sinica | Methods for modifying human antibodies by glycan engineering |
WO2022147463A2 (en) | 2020-12-31 | 2022-07-07 | Alamar Biosciences, Inc. | Binder molecules with high affinity and/ or specificity and methods of making and use thereof |
WO2022147147A1 (en) | 2020-12-30 | 2022-07-07 | Abbott Laboratories | Methods for determining sars-cov-2 antigen and anti-sars-cov-2 antibody in a sample |
WO2022159590A1 (en) | 2021-01-20 | 2022-07-28 | Visterra, Inc. | Interleukin-2 mutants and uses thereof |
WO2022162569A1 (en) | 2021-01-29 | 2022-08-04 | Novartis Ag | Dosage regimes for anti-cd73 and anti-entpd2 antibodies and uses thereof |
WO2022182872A2 (en) | 2021-02-24 | 2022-09-01 | Alladapt Immunotherapeutics, Inc. | Compositions and methods for identification of cross-reactive allergenic proteins and treatment of allergies |
WO2022187440A1 (en) | 2021-03-03 | 2022-09-09 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | La protien as a novel regulator of osteoclastogenesis |
US11447809B2 (en) | 2017-07-06 | 2022-09-20 | President And Fellows Of Harvard College | Evolution of tRNA synthetases |
WO2022195551A1 (en) | 2021-03-18 | 2022-09-22 | Novartis Ag | Biomarkers for cancer and methods of use thereof |
WO2022204581A2 (en) | 2021-03-26 | 2022-09-29 | Scholar Rock, Inc. | Tgf-beta inhibitors and use thereof |
WO2022215011A1 (en) | 2021-04-07 | 2022-10-13 | Novartis Ag | USES OF ANTI-TGFβ ANTIBODIES AND OTHER THERAPEUTIC AGENTS FOR THE TREATMENT OF PROLIFERATIVE DISEASES |
WO2022216993A2 (en) | 2021-04-08 | 2022-10-13 | Marengo Therapeutics, Inc. | Multifuntional molecules binding to tcr and uses thereof |
US11471537B2 (en) | 2017-04-05 | 2022-10-18 | Novo Nordisk A/S | Oligomer extended insulin-Fc conjugates |
WO2022245920A1 (en) | 2021-05-18 | 2022-11-24 | Abbott Laboratories | Methods of evaluating brain injury in a pediatric subject |
WO2022256723A2 (en) | 2021-06-03 | 2022-12-08 | Scholar Rock, Inc. | Tgf-beta inhibitors and therapeutic use thereof |
US11524983B2 (en) | 2015-07-23 | 2022-12-13 | President And Fellows Of Harvard College | Evolution of Bt toxins |
WO2022261018A1 (en) | 2021-06-07 | 2022-12-15 | Providence Health & Services - Oregon | Cxcr5, pd-1, and icos expressing tumor reactive cd4 t cells and their use |
WO2022261183A2 (en) | 2021-06-08 | 2022-12-15 | Dana-Farber Cancer Institute, Inc. | Compositions and methods for treating and/or identifying an agent for treating intestinal cancers |
WO2022266034A1 (en) | 2021-06-14 | 2022-12-22 | Abbott Laboratories | Methods of diagnosing or aiding in diagnosis of brain injury caused by acoustic energy, electromagnetic energy, an over pressurization wave, and/or blast wind |
WO2022271867A1 (en) | 2021-06-23 | 2022-12-29 | Scholar Rock, Inc. | A myostatin pathway inhibitor in combination with a glp-1 pathway activator for use in treating metabolic disorders |
WO2023288267A1 (en) | 2021-07-14 | 2023-01-19 | 2Seventy Bio, Inc. | Engineered t cell receptors fused to binding domains from antibodies |
WO2023018803A1 (en) | 2021-08-10 | 2023-02-16 | Byomass Inc. | Anti-gdf15 antibodies, compositions and uses thereof |
US11583577B2 (en) | 2016-04-22 | 2023-02-21 | Obi Pharma, Inc. | Cancer immunotherapy by immune activation or immune modulation via Globo series antigens |
WO2023025927A1 (en) | 2021-08-26 | 2023-03-02 | Glycanostics S.R.O | Glycoprotein biomarkers for diagnosing cancer |
US11596620B2 (en) | 2013-03-13 | 2023-03-07 | F. Hoffmann-La Roche Ag | Formulations with reduced oxidation |
WO2023034777A1 (en) | 2021-08-31 | 2023-03-09 | Abbott Laboratories | Methods and systems of diagnosing brain injury |
WO2023044483A2 (en) | 2021-09-20 | 2023-03-23 | Voyager Therapeutics, Inc. | Compositions and methods for the treatment of her2 positive cancer |
WO2023044094A1 (en) | 2021-09-20 | 2023-03-23 | Alnylam Pharmaceuticals, Inc. | Inhibin subunit beta e (inhbe) modulator compositions and methods of use thereof |
WO2023041565A1 (en) | 2021-09-14 | 2023-03-23 | Glycanostics S.R.O | Use of lectins to determine mammaglobin-a glycoforms in breast cancer |
WO2023056069A1 (en) | 2021-09-30 | 2023-04-06 | Angiex, Inc. | Degrader-antibody conjugates and methods of using same |
WO2023056268A1 (en) | 2021-09-30 | 2023-04-06 | Abbott Laboratories | Methods and systems of diagnosing brain injury |
US11623945B2 (en) | 2017-02-06 | 2023-04-11 | The United States Of America, As Represented By The Secretary Of Agriculture | Immunostimulating compositions and uses therefore |
US11624130B2 (en) | 2017-09-18 | 2023-04-11 | President And Fellows Of Harvard College | Continuous evolution for stabilized proteins |
WO2023069421A1 (en) | 2021-10-18 | 2023-04-27 | Byomass Inc. | Anti-activin a antibodies, compositions and uses thereof |
US11642400B2 (en) | 2016-07-27 | 2023-05-09 | Obi Pharma, Inc. | Immunogenic/therapeutic glycan compositions and uses thereof |
US11643456B2 (en) | 2016-07-29 | 2023-05-09 | Obi Pharma, Inc. | Human antibodies, pharmaceutical compositions and methods |
US11649285B2 (en) | 2016-08-03 | 2023-05-16 | Bio-Techne Corporation | Identification of VSIG3/VISTA as a novel immune checkpoint and use thereof for immunotherapy |
WO2023092004A1 (en) | 2021-11-17 | 2023-05-25 | Voyager Therapeutics, Inc. | Compositions and methods for the treatment of tau-related disorders |
WO2023097119A2 (en) | 2021-11-29 | 2023-06-01 | Dana-Farber Cancer Institute, Inc. | Methods and compositions to modulate riok2 |
WO2023097254A1 (en) | 2021-11-24 | 2023-06-01 | Visterra, Inc. | Engineered antibody molecules to cd138 and uses thereof |
WO2023102384A1 (en) | 2021-11-30 | 2023-06-08 | Abbott Laboratories | Use of one or more biomarkers to determine traumatic brain injury (tbi) in a subject having received a head computerized tomography scan that is negative for a tbi |
WO2023102463A1 (en) | 2021-12-01 | 2023-06-08 | Visterra, Inc. | Methods of using interleukin-2 agents |
WO2023114978A1 (en) | 2021-12-17 | 2023-06-22 | Abbott Laboratories | Systems and methods for determining uch-l1, gfap, and other biomarkers in blood samples |
WO2023118508A1 (en) | 2021-12-23 | 2023-06-29 | Bavarian Nordic A/S | Recombinant mva viruses for intraperitoneal administration for treating cancer |
WO2023122213A1 (en) | 2021-12-22 | 2023-06-29 | Byomass Inc. | Targeting gdf15-gfral pathway cross-reference to related applications |
WO2023129942A1 (en) | 2021-12-28 | 2023-07-06 | Abbott Laboratories | Use of biomarkers to determine sub-acute traumatic brain injury (tbi) in a subject having received a head computerized tomography (ct) scan that is negative for a tbi or no head ct scan |
US11708411B2 (en) | 2013-12-20 | 2023-07-25 | Wake Forest University Health Sciences | Methods and compositions for increasing protective antibody levels induced by pneumococcal polysaccharide vaccines |
EP4218817A2 (en) | 2017-01-06 | 2023-08-02 | Scholar Rock, Inc. | Methods for treating metabolic diseases by inhibiting myostatin activation |
WO2023147107A1 (en) | 2022-01-31 | 2023-08-03 | Byomass Inc. | Myeloproliferative conditions |
WO2023150652A1 (en) | 2022-02-04 | 2023-08-10 | Abbott Laboratories | Lateral flow methods, assays, and devices for detecting the presence or measuring the amount of ubiquitin carboxy-terminal hydrolase l1 and/or glial fibrillary acidic protein in a sample |
WO2023150778A1 (en) | 2022-02-07 | 2023-08-10 | Visterra, Inc. | Anti-idiotype antibody molecules and uses thereof |
US11725247B2 (en) | 2016-02-29 | 2023-08-15 | Foundation Medicine, Inc. | Methods of treating cancer |
US11738050B2 (en) | 2019-02-01 | 2023-08-29 | Regents Of The University Of Minnesota | Compounds binding to fibroblast activation protein alpha |
WO2023212518A1 (en) | 2022-04-25 | 2023-11-02 | Visterra, Inc. | Antibody molecules to april and uses thereof |
WO2023220695A2 (en) | 2022-05-13 | 2023-11-16 | Voyager Therapeutics, Inc. | Compositions and methods for the treatment of her2 positive cancer |
US11827720B2 (en) | 2006-07-05 | 2023-11-28 | F-Star Therapeutics Limited | Multivalent immunoglobulins |
WO2023239803A1 (en) | 2022-06-08 | 2023-12-14 | Angiex, Inc. | Anti-tm4sf1 antibody-drug conjugates comprising cleavable linkers and methods of using same |
EP4296279A1 (en) | 2022-06-23 | 2023-12-27 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Anti-transthyretin (ttr) binding proteins and uses thereof |
WO2024006876A1 (en) | 2022-06-29 | 2024-01-04 | Abbott Laboratories | Magnetic point-of-care systems and assays for determining gfap in biological samples |
WO2024013727A1 (en) | 2022-07-15 | 2024-01-18 | Janssen Biotech, Inc. | Material and methods for improved bioengineered pairing of antigen-binding variable regions |
US11884739B2 (en) | 2014-05-27 | 2024-01-30 | Academia Sinica | Anti-CD20 glycoantibodies and uses thereof |
WO2024030976A2 (en) | 2022-08-03 | 2024-02-08 | Voyager Therapeutics, Inc. | Compositions and methods for crossing the blood brain barrier |
EP4324518A2 (en) | 2014-01-31 | 2024-02-21 | Novartis AG | Antibody molecules to tim-3 and uses thereof |
US11913044B2 (en) | 2018-06-14 | 2024-02-27 | President And Fellows Of Harvard College | Evolution of cytidine deaminases |
Families Citing this family (1434)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE164395T1 (en) * | 1990-12-03 | 1998-04-15 | Genentech Inc | METHOD FOR ENRICHMENT OF PROTEIN VARIANTS WITH MODIFIED BINDING PROPERTIES |
CA2108147C (en) | 1991-04-10 | 2009-01-06 | Angray Kang | Heterodimeric receptor libraries using phagemids |
US6800738B1 (en) * | 1991-06-14 | 2004-10-05 | Genentech, Inc. | Method for making humanized antibodies |
EP0940468A1 (en) | 1991-06-14 | 1999-09-08 | Genentech, Inc. | Humanized antibody variable domain |
US6406855B1 (en) | 1994-02-17 | 2002-06-18 | Maxygen, Inc. | Methods and compositions for polypeptide engineering |
US6335160B1 (en) | 1995-02-17 | 2002-01-01 | Maxygen, Inc. | Methods and compositions for polypeptide engineering |
US5837458A (en) * | 1994-02-17 | 1998-11-17 | Maxygen, Inc. | Methods and compositions for cellular and metabolic engineering |
US7597886B2 (en) * | 1994-11-07 | 2009-10-06 | Human Genome Sciences, Inc. | Tumor necrosis factor-gamma |
US7820798B2 (en) * | 1994-11-07 | 2010-10-26 | Human Genome Sciences, Inc. | Tumor necrosis factor-gamma |
US7429646B1 (en) | 1995-06-05 | 2008-09-30 | Human Genome Sciences, Inc. | Antibodies to human tumor necrosis factor receptor-like 2 |
US6475806B1 (en) | 1995-06-07 | 2002-11-05 | Praecis Pharmaceuticals, Inc. | Anchor libraries and identification of peptide binding sequences |
US7888466B2 (en) | 1996-01-11 | 2011-02-15 | Human Genome Sciences, Inc. | Human G-protein chemokine receptor HSATU68 |
US20070185032A1 (en) * | 1996-12-11 | 2007-08-09 | Praecis Pharmaceuticals, Inc. | Pharmaceutical formulations for sustained drug delivery |
US6172213B1 (en) * | 1997-07-02 | 2001-01-09 | Genentech, Inc. | Anti-IgE antibodies and method of improving polypeptides |
US5994511A (en) * | 1997-07-02 | 1999-11-30 | Genentech, Inc. | Anti-IgE antibodies and methods of improving polypeptides |
US7192589B2 (en) | 1998-09-16 | 2007-03-20 | Genentech, Inc. | Treatment of inflammatory disorders with STIgMA immunoadhesins |
CA2309358A1 (en) | 1997-11-21 | 1999-06-03 | Genentech, Inc. | A-33 related antigens and their pharmacological uses |
AU3072799A (en) | 1998-03-19 | 1999-10-11 | Human Genome Sciences, Inc. | Cytokine receptor common gamma chain like |
ES2316194T3 (en) * | 1998-10-28 | 2009-04-01 | Cornell Research Foundation, Inc. | METHODS FOR THE REGULATION OF ANGIOGENESIS AND VASCULAR INTEGRITY USING THE BDNF, NT-3 AND NT-4 LIGANDS. |
US6927024B2 (en) | 1998-11-30 | 2005-08-09 | Genentech, Inc. | PCR assay |
US6696063B1 (en) * | 1998-12-30 | 2004-02-24 | Applied Research Systems Ars Holding N.V. | Treatment of HIV-associated dysmorphia/dysmetabolic syndrome (HADDS) with or without lipodystrophy |
WO2000039302A2 (en) * | 1998-12-31 | 2000-07-06 | Chiron Corporation | Improved expression of hiv polypeptides and production of virus-like particles |
JP2003523721A (en) | 1998-12-31 | 2003-08-12 | カイロン コーポレイション | Polynucleotides encoding antigenic HIVC-type polypeptides, polypeptides, and uses thereof |
US7935805B1 (en) | 1998-12-31 | 2011-05-03 | Novartis Vaccines & Diagnostics, Inc | Polynucleotides encoding antigenic HIV Type C polypeptides, polypeptides and uses thereof |
DK1141315T3 (en) | 1998-12-31 | 2008-05-19 | Novartis Vaccines & Diagnostic | Modified HIV Env polypeptides |
EP1141014B1 (en) | 1999-01-06 | 2004-12-08 | Genentech, Inc. | Insulin-like growth factor (igf) i mutant variant |
WO2000040612A1 (en) * | 1999-01-06 | 2000-07-13 | Genentech, Inc. | Insulin-like growth factor (igf) i mutant variants |
CA2363779A1 (en) | 1999-02-26 | 2000-08-31 | Human Genome Sciences, Inc. | Human endokine alpha and methods of use |
AU4057600A (en) * | 1999-03-31 | 2000-10-16 | Rosetta Inpharmatics, Inc. | Methods for the identification of reporter and target molecules using comprehensive gene expression profiles |
US7270969B2 (en) | 1999-05-05 | 2007-09-18 | Phylogica Limited | Methods of constructing and screening diverse expression libraries |
US7803765B2 (en) * | 1999-05-05 | 2010-09-28 | Phylogica Limited | Methods of constructing biodiverse gene fragment libraries and biological modulators isolated therefrom |
CA2372464C (en) | 1999-05-05 | 2012-07-31 | Tvw Telethon Institute For Child Health Research | Isolating biological modulators from biodiverse gene fragment libraries |
US6200803B1 (en) | 1999-05-21 | 2001-03-13 | Rosetta Inpharmatics, Inc. | Essential genes of yeast as targets for antifungal agents, herbicides, insecticides and anti-proliferative drugs |
US6197517B1 (en) | 1999-05-21 | 2001-03-06 | Rosetta Inpharmatics, Inc. | Essential genes of yeast as targets for antifungal agents, herbicides, insecticides and anti-proliferative drugs |
US6221597B1 (en) | 1999-05-21 | 2001-04-24 | Rosetta Inpharmatics, Inc. | Essential genes of yeast as targets for antifungal agents, herbicides, insecticides and anti-proliferative drugs |
US20030166003A1 (en) * | 1999-06-14 | 2003-09-04 | Cochran Andrea G. | Structured peptide scaffold for displaying turn libraries on phage |
ES2242620T3 (en) | 1999-06-14 | 2005-11-16 | Genentech, Inc. | PEPTIDIC STRUCTURES TO DISPLAY LIBRARIES OF TURNS OF A PAYMENT. |
DE19943743C2 (en) * | 1999-09-03 | 2002-02-07 | Jerini Biotools Gmbh | Procedure for the identification of binding partners with position-specific arrays |
CN1279054C (en) * | 1999-10-20 | 2006-10-11 | 杰南技术公司 | Type I cytokine receptor TCCR |
US20060073509A1 (en) * | 1999-11-18 | 2006-04-06 | Michael Kilpatrick | Method for detecting and quantitating multiple subcellular components |
AU784983B2 (en) * | 1999-12-15 | 2006-08-17 | Genentech Inc. | Shotgun scanning, a combinatorial method for mapping functional protein epitopes |
US20020004247A1 (en) * | 1999-12-23 | 2002-01-10 | Genentech, Inc. | Assay method |
CA2403425C (en) | 2000-04-11 | 2013-08-27 | Genentech, Inc. | Multivalent antibodies and uses therefor |
ES2529300T3 (en) | 2000-04-12 | 2015-02-18 | Novozymes Biopharma Dk A/S | Albumin fusion proteins |
US8288322B2 (en) | 2000-04-17 | 2012-10-16 | Dyax Corp. | Methods of constructing libraries comprising displayed and/or expressed members of a diverse family of peptides, polypeptides or proteins and the novel libraries |
US20040029113A1 (en) * | 2000-04-17 | 2004-02-12 | Ladner Robert C. | Novel methods of constructing libraries of genetic packages that collectively display the members of a diverse family of peptides, polypeptides or proteins |
US7297762B2 (en) * | 2000-04-24 | 2007-11-20 | Yale University | Modified avian pancreatic polypeptide miniature binding proteins |
US7495070B2 (en) * | 2000-04-24 | 2009-02-24 | Yale University | Protein binding miniature proteins |
WO2001087323A2 (en) | 2000-05-16 | 2001-11-22 | Genentech, Inc. | Method for treating cartilage disorders |
US20030031675A1 (en) | 2000-06-06 | 2003-02-13 | Mikesell Glen E. | B7-related nucleic acids and polypeptides useful for immunomodulation |
EP1294949A4 (en) | 2000-06-15 | 2004-08-25 | Human Genome Sciences Inc | Human tumor necrosis factor delta and epsilon |
KR101287395B1 (en) | 2000-06-16 | 2014-11-04 | 휴먼 게놈 사이언시즈, 인코포레이티드 | Antibodies that immunospecifically bind to BLyS |
BR0111298A (en) * | 2000-06-28 | 2005-05-10 | Bristol Myers Squibb Co | Selective androgen receptor modulators and methods for their identification, design and use |
US6951947B2 (en) * | 2000-07-13 | 2005-10-04 | The Scripps Research Institute | Labeled peptides, proteins and antibodies and processes and intermediates useful for their preparation |
US7176037B2 (en) * | 2000-07-13 | 2007-02-13 | The Scripps Research Institute | Labeled peptides, proteins and antibodies and processes and intermediates useful for their preparation |
DE60136816D1 (en) | 2000-07-27 | 2009-01-15 | Genentech Inc | SEQUENTIAL ADMINISTRATION OF CPT-11 AND APO-2L POLYPEPTIDE |
US20080194022A1 (en) * | 2000-08-03 | 2008-08-14 | Clarke Michael F | Isolation and use of solid tumor stem cells |
US6984522B2 (en) | 2000-08-03 | 2006-01-10 | Regents Of The University Of Michigan | Isolation and use of solid tumor stem cells |
US8044259B2 (en) | 2000-08-03 | 2011-10-25 | The Regents Of The University Of Michigan | Determining the capability of a test compound to affect solid tumor stem cells |
US6902734B2 (en) | 2000-08-07 | 2005-06-07 | Centocor, Inc. | Anti-IL-12 antibodies and compositions thereof |
TWI283182B (en) | 2000-08-07 | 2007-07-01 | Nektar Therapeutics | Inhalable spray dried 4-helix bundle protein powders having minimized aggregation |
UA81743C2 (en) | 2000-08-07 | 2008-02-11 | Центокор, Инк. | HUMAN MONOCLONAL ANTIBODY WHICH SPECIFICALLY BINDS TUMOR NECROSIS FACTOR ALFA (TNFα), PHARMACEUTICAL MIXTURE CONTAINING THEREOF, AND METHOD FOR TREATING ARTHRITIS |
US7288390B2 (en) | 2000-08-07 | 2007-10-30 | Centocor, Inc. | Anti-dual integrin antibodies, compositions, methods and uses |
ATE552859T1 (en) * | 2000-09-13 | 2012-04-15 | Praecis Pharm Inc | PHARMACEUTICAL FORMULATIONS FOR CONTINUOUS DELIVERY OF PEPTIDES |
GB0022978D0 (en) | 2000-09-19 | 2000-11-01 | Oxford Glycosciences Uk Ltd | Detection of peptides |
ATE402958T1 (en) | 2000-09-26 | 2008-08-15 | Genentech Inc | ANTAGONISTS OF THE IGE RECEPTOR |
US7393532B1 (en) | 2000-10-18 | 2008-07-01 | Genentech, Inc. | Modulation of T cell differentiation for the treatment of T helper cell mediated diseases |
US6673580B2 (en) | 2000-10-27 | 2004-01-06 | Genentech, Inc. | Identification and modification of immunodominant epitopes in polypeptides |
US6841359B2 (en) * | 2000-10-31 | 2005-01-11 | The General Hospital Corporation | Streptavidin-binding peptides and uses thereof |
TWI327600B (en) | 2000-11-28 | 2010-07-21 | Medimmune Llc | Methods of administering/dosing anti-rsv antibodies for prophylaxis and treatment |
US20040253242A1 (en) * | 2000-12-05 | 2004-12-16 | Bowdish Katherine S. | Rationally designed antibodies |
US7396917B2 (en) * | 2000-12-05 | 2008-07-08 | Alexion Pharmaceuticals, Inc. | Rationally designed antibodies |
DE60136656D1 (en) | 2000-12-05 | 2009-01-02 | Alexion Pharma Inc | Rationally designed antibodies |
US9249229B2 (en) * | 2000-12-08 | 2016-02-02 | Alexion Pharmaceuticals, Inc. | Polypeptides and antibodies derived from chronic lymphocytic leukemia cells and uses thereof |
US20060057651A1 (en) | 2000-12-08 | 2006-03-16 | Bowdish Katherine S | Polypeptides and antibodies derived from chronic lymphocytic leukemia cells and uses thereof |
EP1341902A2 (en) * | 2000-12-08 | 2003-09-10 | Alexion Pharmaceuticals, Inc. | Chronic lymphocytic leukemia cell line and its use for producing an antibody |
US7408041B2 (en) * | 2000-12-08 | 2008-08-05 | Alexion Pharmaceuticals, Inc. | Polypeptides and antibodies derived from chronic lymphocytic leukemia cells and uses thereof |
US20040198661A1 (en) * | 2000-12-08 | 2004-10-07 | Bowdish Katherine S. | Polypeptides and antibodies derived from chronic lymphocytic leukemia cells and uses thereof |
EP2357187A1 (en) | 2000-12-12 | 2011-08-17 | MedImmune, LLC | Molecules with extended half-lives, compositions and uses thereof |
AU2002249854B2 (en) | 2000-12-18 | 2007-09-20 | Dyax Corp. | Focused libraries of genetic packages |
ATE519783T1 (en) * | 2000-12-22 | 2011-08-15 | Grad Carole Legal Representative Of Kaplan Howard | ßPHAGE DISPLAYß LIBRARY OF HUMAN VH FRAGMENTS |
EP1355666B1 (en) | 2000-12-22 | 2012-06-13 | Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. | Use of repulsive guidance molecule (RGM) and its modulators |
CA2437811A1 (en) | 2001-02-09 | 2002-08-22 | Human Genome Sciences, Inc. | Human g-protein chemokine receptor (ccr5) hdgnr10 |
US20030044406A1 (en) * | 2001-03-02 | 2003-03-06 | Christine Dingivan | Methods of preventing or treating inflammatory or autoimmune disorders by administering CD2 antagonists in combination with other prophylactic or therapeutic agents |
CA2342376C (en) * | 2001-03-20 | 2013-11-12 | Marco Colonna | A receptor trem (triggering receptor expressed on myeloid cells) and uses thereof |
US8231878B2 (en) * | 2001-03-20 | 2012-07-31 | Cosmo Research & Development S.P.A. | Receptor trem (triggering receptor expressed on myeloid cells) and uses thereof |
US20090081199A1 (en) * | 2001-03-20 | 2009-03-26 | Bioxell S.P.A. | Novel receptor trem (triggering receptor expressed on myeloid cells) and uses thereof |
US8981061B2 (en) | 2001-03-20 | 2015-03-17 | Novo Nordisk A/S | Receptor TREM (triggering receptor expressed on myeloid cells) and uses thereof |
CA2444632A1 (en) | 2001-04-13 | 2002-10-24 | Human Genome Sciences, Inc. | Vascular endothelial growth factor 2 |
US6914123B2 (en) * | 2001-04-17 | 2005-07-05 | Genentech, Inc. | Hairpin peptides with a novel structural motif and methods relating thereto |
EP1572874B1 (en) | 2001-05-25 | 2013-09-18 | Human Genome Sciences, Inc. | Antibodies that immunospecifically bind to trail receptors |
US20060239533A1 (en) * | 2001-06-04 | 2006-10-26 | Triantafyllos Tafas | Method for detecting infectious agents using computer controlled automated image analysis |
US20030148380A1 (en) * | 2001-06-05 | 2003-08-07 | Belcher Angela M. | Molecular recognition of materials |
US20050164515A9 (en) * | 2001-06-05 | 2005-07-28 | Belcher Angela M. | Biological control of nanoparticle nucleation, shape and crystal phase |
US20030113714A1 (en) * | 2001-09-28 | 2003-06-19 | Belcher Angela M. | Biological control of nanoparticles |
US20070160576A1 (en) | 2001-06-05 | 2007-07-12 | Genentech, Inc. | IL-17A/F heterologous polypeptides and therapeutic uses thereof |
US7803915B2 (en) * | 2001-06-20 | 2010-09-28 | Genentech, Inc. | Antibody compositions for the diagnosis and treatment of tumor |
US20050107595A1 (en) * | 2001-06-20 | 2005-05-19 | Genentech, Inc. | Compositions and methods for the diagnosis and treatment of tumor |
ATE522623T1 (en) | 2001-06-20 | 2011-09-15 | Genentech Inc | COMPOSITIONS AND METHODS FOR THE TREATMENT AND DIAGNOSIS OF LUNG TUMORS |
EP1409694A4 (en) * | 2001-07-05 | 2006-02-08 | Chiron Corp | Polynucleotides encoding antigenic hiv type b and/or type c polypeptides, polypeptides and uses thereof |
CA2452015C (en) | 2001-07-05 | 2012-07-03 | Chiron Corporation | Polynucleotides encoding antigenic hiv type c polypeptides, polypeptides and uses thereof |
DE10135039C1 (en) * | 2001-07-18 | 2003-03-13 | Nemod Immuntherapie Ag | Method for isolating large variances of specific molecules for a target molecule from phagemid gene libraries |
US6867189B2 (en) * | 2001-07-26 | 2005-03-15 | Genset S.A. | Use of adipsin/complement factor D in the treatment of metabolic related disorders |
KR100458083B1 (en) * | 2001-08-29 | 2004-11-18 | 주식회사 아이지세라피 | Method for the construction of phage display library using helper phage variants |
JP2005521380A (en) * | 2001-08-31 | 2005-07-21 | カイロン コーポレイション | Polynucleotide encoding antigenic type B HIV polypeptide, polypeptide and use thereof |
US20030170614A1 (en) * | 2001-08-31 | 2003-09-11 | Megede Jan Zur | Polynucleotides encoding antigenic HIV type B polypeptides, polypeptides and uses thereof |
EP1425040A2 (en) * | 2001-09-14 | 2004-06-09 | Cytos Biotechnology AG | In vivo activation of antigen presenting cells for enhancement of immune responses induced by virus like particles |
EP2153843B1 (en) | 2001-09-18 | 2012-08-15 | Genentech, Inc. | Compositions and methods for the diagnosis and treatment of tumor |
US20030073104A1 (en) * | 2001-10-02 | 2003-04-17 | Belcher Angela M. | Nanoscaling ordering of hybrid materials using genetically engineered mesoscale virus |
WO2005049075A2 (en) | 2003-11-17 | 2005-06-02 | Genentech, Inc. | Compositions and methods for the treatment of tumor of hematopoietic origin |
US20050123925A1 (en) | 2002-11-15 | 2005-06-09 | Genentech, Inc. | Compositions and methods for the diagnosis and treatment of tumor |
EP2261250B1 (en) | 2001-12-21 | 2015-07-01 | Human Genome Sciences, Inc. | GCSF-Albumin fusion proteins |
JP2005525095A (en) | 2002-01-02 | 2005-08-25 | ジェネンテック・インコーポレーテッド | Compositions and methods for tumor diagnosis and treatment |
AU2003207459A1 (en) * | 2002-01-03 | 2003-07-24 | The Scripps Research Institute | Cancer-associated epitope |
US20060046249A1 (en) * | 2002-01-18 | 2006-03-02 | Fei Huang | Identification of polynucleotides and polypetide for predicting activity of compounds that interact with protein tyrosine kinase and or protein tyrosine kinase pathways |
EP1573316B1 (en) | 2002-03-01 | 2009-08-26 | Siemens Healthcare Diagnostics Inc. | Assays for cancer patient monitoring based on levels of epidermal growth factor receptor (egfr) extracellular domain (ecd) analyte, alone or in combination with other analytes, in body fluid samples |
EP1489968B1 (en) * | 2002-03-01 | 2009-02-18 | Siemens Healthcare Diagnostics Inc. | Assays for cancer patient monitoring based on levels of analyte components of the plasminogen activator system in body fluid samples |
AU2003218456A1 (en) * | 2002-04-01 | 2003-10-20 | Human Genome Sciences, Inc. | Antibodies that specifically bind to gmad |
GB0207533D0 (en) | 2002-04-02 | 2002-05-08 | Oxford Glycosciences Uk Ltd | Protein |
WO2003086458A1 (en) | 2002-04-12 | 2003-10-23 | Medimmune, Inc. | Recombinant anti-interleukin-9 antibodies |
EP2011886A3 (en) | 2002-04-16 | 2009-02-11 | Genentech, Inc. | Compositions and methods for the diagnosis and treatment of tumor |
JP4753578B2 (en) * | 2002-06-03 | 2011-08-24 | ジェネンテック, インコーポレイテッド | Synthetic antibody phage library |
CN100418981C (en) * | 2002-06-10 | 2008-09-17 | 瓦西尼斯公司 | Gene differentially expressed in breast and bladder cancer and encoded polypeptides |
US9321992B2 (en) * | 2002-06-14 | 2016-04-26 | Case Western Reserve University | Cell targeting methods and compositions |
US7425618B2 (en) | 2002-06-14 | 2008-09-16 | Medimmune, Inc. | Stabilized anti-respiratory syncytial virus (RSV) antibody formulations |
US20040067532A1 (en) * | 2002-08-12 | 2004-04-08 | Genetastix Corporation | High throughput generation and affinity maturation of humanized antibody |
PT1534335E (en) | 2002-08-14 | 2012-02-28 | Macrogenics Inc | Fcgammariib-specific antibodies and methods of use thereof |
DE10238846A1 (en) * | 2002-08-20 | 2004-03-04 | Nemod Immuntherapie Ag | Active fusion proteins and processes for their production |
KR20050057047A (en) * | 2002-08-29 | 2005-06-16 | 제넨테크, 인크. | Achaete-scute like-2 polypeptides and encoding nucleic acids and methods for the diagnosis and treatment of tumor |
ATE466085T1 (en) * | 2002-09-09 | 2010-05-15 | Hanall Pharmaceutical Co Ltd | PROTEASE-RESISTANT MODIFIED INTERFERON ALPHA POLYPEPTIDES |
US20050064508A1 (en) * | 2003-09-22 | 2005-03-24 | Semzyme | Peptide mediated synthesis of metallic and magnetic materials |
ZA200502612B (en) | 2002-10-08 | 2007-07-25 | Rinat Neuroscience Corp | Methods for treating post-surgical pain by administering a nerve crowth factor antagonist and compositions containing the same |
AU2003304238A1 (en) | 2002-10-08 | 2005-01-13 | Rinat Neuroscience Corp. | Methods for treating post-surgical pain by administering an anti-nerve growth factor antagonist antibody and compositions containing the same |
BR0315157A (en) * | 2002-10-09 | 2005-08-09 | Rinat Neuroscience Corp | Methods of treating alzheimer's disease by employing antibodies directed against amyloid beta peptide and compositions thereof |
PT2301965E (en) | 2002-10-16 | 2015-05-20 | Purdue Pharma Lp | Antibodies that bind cell-associated ca 125/o722p and methods of use thereof |
EP1578799B8 (en) * | 2002-12-02 | 2011-03-23 | Amgen Fremont Inc. | Antibodies directed to tumor necrosis factor and uses thereof |
US7056702B2 (en) * | 2002-12-16 | 2006-06-06 | Kimberly Clark Co | Detecting lipocalin |
US20050089521A1 (en) * | 2002-12-23 | 2005-04-28 | Shelton David L. | Methods for treating taxol-induced sensory neuropathy |
AU2003293958A1 (en) * | 2002-12-23 | 2004-07-22 | Apalexo Biotechnologie Gmbh | Purification of recombinant filamental bacteriophages by means of affinity chromatography to increase the immunogenicity and efficacy of phagic vaccines |
US9498530B2 (en) | 2002-12-24 | 2016-11-22 | Rinat Neuroscience Corp. | Methods for treating osteoarthritis pain by administering a nerve growth factor antagonist and compositions containing the same |
US7569364B2 (en) * | 2002-12-24 | 2009-08-04 | Pfizer Inc. | Anti-NGF antibodies and methods using same |
DK2270048T3 (en) | 2002-12-24 | 2016-01-18 | Rinat Neuroscience Corp | Anti-NGF antibodies and methods for their use |
WO2004065416A2 (en) * | 2003-01-16 | 2004-08-05 | Genentech, Inc. | Synthetic antibody phage libraries |
JP2006518997A (en) * | 2003-01-21 | 2006-08-24 | ブリストル−マイヤーズ スクイブ カンパニー | Novel acyl coenzyme A: polynucleotide encoding monoacylglycerol acyltransferase-3 (MGAT3) and uses thereof |
US7429472B2 (en) | 2003-01-31 | 2008-09-30 | Promega Corporation | Method of immobilizing a protein or molecule via a mutant dehalogenase that is bound to an immobilized dehalogenase substrate and linked directly or indirectly to the protein or molecule |
EP2455458B1 (en) | 2003-01-31 | 2015-01-07 | Promega Corporation | Covalent tethering of functional groups to proteins |
EP1594441B1 (en) | 2003-02-19 | 2010-12-15 | Rinat Neuroscience Corp. | Method for treating pain by administering a nerve growth factor antagonist and an nsaid and composition containing the same |
CA2516455C (en) | 2003-02-20 | 2012-05-01 | Seattle Genetics, Inc. | Anti-cd70 antibody-drug conjugates and their use for the treatment of cancer and immune disorders |
MXPA05009913A (en) * | 2003-03-19 | 2005-11-04 | Biogen Idec Inc | Nogo receptor binding protein. |
WO2004084836A2 (en) * | 2003-03-20 | 2004-10-07 | Rinat Neuroscience Corp. | Methods for treating taxol-induced gut disorder |
US7294701B2 (en) * | 2003-04-02 | 2007-11-13 | Technion Research & Development Foundation Ltd. | Antibody fragment capable of modulating multidrug resistance and compositions and kits and methods using same |
KR20110094361A (en) | 2003-04-11 | 2011-08-23 | 메디뮨 엘엘씨 | Recombinant il-9 antibodies and uses thereof |
TWI353991B (en) | 2003-05-06 | 2011-12-11 | Syntonix Pharmaceuticals Inc | Immunoglobulin chimeric monomer-dimer hybrids |
CN1829741A (en) | 2003-05-30 | 2006-09-06 | 健泰科生物技术公司 | Treatment with anti-VEGF antibodies |
US9708410B2 (en) | 2003-05-30 | 2017-07-18 | Janssen Biotech, Inc. | Anti-tissue factor antibodies and compositions |
CA2528343A1 (en) | 2003-06-06 | 2005-01-06 | Genentech, Inc. | Modulating the interaction between hgf beta chain and c-met |
US20060019256A1 (en) * | 2003-06-09 | 2006-01-26 | The Regents Of The University Of Michigan | Compositions and methods for treating and diagnosing cancer |
SI1641822T1 (en) | 2003-07-08 | 2013-08-30 | Genentech, Inc. | Il-17 a/f heterologous polypeptides and therapeutic uses thereof |
WO2005010163A2 (en) * | 2003-07-15 | 2005-02-03 | Barros Research Institute | Compositions and methods for immunotherapy of human immunotherapy of human immunodeficiency virus (hiv) |
AU2004259727A1 (en) * | 2003-07-15 | 2005-02-03 | Barros Research Institute | Compositions and methods for immunotherapy of cancer and infectious diseases. |
US7727752B2 (en) | 2003-07-29 | 2010-06-01 | Life Technologies Corporation | Kinase and phosphatase assays |
US7758859B2 (en) * | 2003-08-01 | 2010-07-20 | Genentech, Inc. | Anti-VEGF antibodies |
US20050106667A1 (en) * | 2003-08-01 | 2005-05-19 | Genentech, Inc | Binding polypeptides with restricted diversity sequences |
EP1668111A4 (en) | 2003-08-08 | 2008-07-02 | Genenews Inc | Osteoarthritis biomarkers and uses thereof |
JP4934426B2 (en) | 2003-08-18 | 2012-05-16 | メディミューン,エルエルシー | Antibody humanization |
BRPI0414093A (en) | 2003-09-05 | 2006-10-31 | Scripps Res Insittute | cholesterol ozonation products for the treatment and prevention of atherosclerosis and / or cardiovascular disease |
MXPA06002563A (en) * | 2003-09-05 | 2006-06-20 | Scripps Research Inst | Detection of cholesterol ozonation products. |
IL158287A0 (en) | 2003-10-07 | 2004-05-12 | Yeda Res & Dev | Antibodies to nik, their preparation and use |
US7329725B1 (en) * | 2003-10-29 | 2008-02-12 | Nastech Pharmaceutical Company Inc. | Phage displayed Trp cage ligands |
GB0325836D0 (en) * | 2003-11-05 | 2003-12-10 | Celltech R&D Ltd | Biological products |
AU2004290070A1 (en) | 2003-11-12 | 2005-05-26 | Biogen Idec Ma Inc. | Neonatal Fc receptor (FcRn)-binding polypeptide variants, dimeric Fc binding proteins and methods related thereto |
DK1983000T3 (en) * | 2003-11-21 | 2015-12-07 | Ucb Biopharma Sprl | A method for the treatment of multiple sclerosis by inhibiting IL-17 activity |
WO2005055936A2 (en) * | 2003-12-04 | 2005-06-23 | Vaccinex, Inc. | Methods of killing tumor cells by targeting internal antigens exposed on apoptotic tumor cells |
CA2548282A1 (en) | 2003-12-11 | 2005-06-30 | Genentech, Inc. | Methods and compositions for inhibiting c-met dimerization and activation |
GB0329825D0 (en) * | 2003-12-23 | 2004-01-28 | Celltech R&D Ltd | Biological products |
JP4503617B2 (en) | 2003-12-23 | 2010-07-14 | ライナット ニューロサイエンス コーポレイション | Agonist anti-trkC antibody and method using the antibody |
US20050266425A1 (en) * | 2003-12-31 | 2005-12-01 | Vaccinex, Inc. | Methods for producing and identifying multispecific antibodies |
JP4782700B2 (en) | 2004-01-20 | 2011-09-28 | カロバイオス ファーマシューティカルズ インコーポレイティッド | Transfer of antibody specificity using minimally required binding determinants |
CN103755800B (en) * | 2004-02-02 | 2016-02-24 | Ambrx公司 | Modified human interferon polypeptides and its purposes |
US20050232927A1 (en) * | 2004-02-03 | 2005-10-20 | The Regents Of The University Of Michigan | Compositions and methods for characterizing, regulating, diagnosing, and treating cancer |
SI1729795T1 (en) | 2004-02-09 | 2016-04-29 | Human Genome Sciences, Inc. | Albumin fusion proteins |
ATE452147T1 (en) | 2004-02-19 | 2010-01-15 | Genentech Inc | ANTIBODIES WITH CORRECTED CDR |
EP1735453A2 (en) * | 2004-03-12 | 2006-12-27 | The Scripps Research Institute | Fluorescent signal emitting live cell biosensor molecules and dyes for detection and quantification of protein activities |
US7973139B2 (en) * | 2004-03-26 | 2011-07-05 | Human Genome Sciences, Inc. | Antibodies against nogo receptor |
JP5128935B2 (en) | 2004-03-31 | 2013-01-23 | ジェネンテック, インコーポレイテッド | Humanized anti-TGF-β antibody |
ATE456580T1 (en) * | 2004-04-07 | 2010-02-15 | Rinat Neuroscience Corp | METHOD FOR PAIN TREATMENT IN BONE CANCER BY ADMINISTRATION OF A NGF ANTAGONIST |
US7794713B2 (en) | 2004-04-07 | 2010-09-14 | Lpath, Inc. | Compositions and methods for the treatment and prevention of hyperproliferative diseases |
US7785903B2 (en) * | 2004-04-09 | 2010-08-31 | Genentech, Inc. | Variable domain library and uses |
CA2955027A1 (en) | 2004-04-15 | 2005-11-10 | University Of Florida Research Foundation, Inc. | Neural proteins as biomarkers for nervous system injury and other neural disorders |
CA2558963A1 (en) * | 2004-04-16 | 2005-12-15 | Genentech, Inc. | Omi pdz modulators |
ES2442386T3 (en) | 2004-04-23 | 2014-02-11 | Bundesrepublik Deutschland Letztvertreten Durch Das Robert Koch-Institut Vertreten Durch Seinen Pr | Method for the treatment of conditions mediated by T cells by the decrease of positive ICOS cells in vivo. |
US20060292554A1 (en) * | 2004-05-18 | 2006-12-28 | Genentech, Inc. | Major coat protein variants for C-terminal and bi-terminal display |
EP1602928A1 (en) * | 2004-06-01 | 2005-12-07 | Universiteit Maastricht | Process and kit for determining binding parameters of bioaffinity binding reactions |
DK1754052T3 (en) * | 2004-06-03 | 2015-09-28 | Phylogica Ltd | Modulators with biochemical properties |
US7604947B2 (en) * | 2004-06-09 | 2009-10-20 | Cornell Research Foundation, Inc. | Detection and modulation of cancer stem cells |
CN102603895B (en) * | 2004-06-18 | 2016-09-28 | Ambrx公司 | Novel antigen-binding polypeptides and its purposes |
PT1776136E (en) | 2004-06-24 | 2012-12-05 | Biogen Idec Inc | Treatment of conditions involving demyelination |
US6986264B1 (en) * | 2004-07-15 | 2006-01-17 | Carrier Corporation | Economized dehumidification system |
US8604185B2 (en) | 2004-07-20 | 2013-12-10 | Genentech, Inc. | Inhibitors of angiopoietin-like 4 protein, combinations, and their use |
DE602005019167D1 (en) * | 2004-07-20 | 2010-03-18 | Genentech Inc | ANGIOPOIETIN-LIKE 4 PROTEIN HEMMER COMBINATIONS AND THEIR USE |
AU2005327906B2 (en) * | 2004-07-21 | 2010-05-13 | Ambrx, Inc. | Biosynthetic polypeptides utilizing non-naturally encoded amino acids |
US20070087400A1 (en) * | 2004-07-30 | 2007-04-19 | Aldis Darzins | Covalent tethering of functional groups to proteins and substrates therefor |
KR20070040824A (en) | 2004-07-30 | 2007-04-17 | 리나트 뉴로사이언스 코퍼레이션 | Antibodies directed against amyloid-beta peptide and methods using same |
US7425436B2 (en) * | 2004-07-30 | 2008-09-16 | Promega Corporation | Covalent tethering of functional groups to proteins and substrates therefor |
EP1789070B1 (en) | 2004-08-03 | 2012-10-24 | Biogen Idec MA Inc. | Taj in neuronal function |
HUE058817T2 (en) | 2004-09-03 | 2022-09-28 | Genentech Inc | Humanized anti-beta7 antagonists and uses therefor |
JP2008513540A (en) | 2004-09-21 | 2008-05-01 | メディミューン,インコーポレーテッド | Antibody to respiratory syncytial virus and method for producing vaccine for the virus |
WO2006047417A2 (en) | 2004-10-21 | 2006-05-04 | University Of Florida Research Foundation, Inc. | Detection of cannabinoid receptor biomarkers and uses thereof |
NZ590132A (en) | 2004-10-21 | 2012-03-30 | Genentech Inc | Dosage regime for treating intraocular neovascular diseases with VEGF |
JP2008518023A (en) | 2004-10-27 | 2008-05-29 | メディミューン,インコーポレーテッド | Regulation of antibody specificity by altering affinity for cognate antigens |
US7998930B2 (en) | 2004-11-04 | 2011-08-16 | Hanall Biopharma Co., Ltd. | Modified growth hormones |
GB0426146D0 (en) | 2004-11-29 | 2004-12-29 | Bioxell Spa | Therapeutic peptides and method |
KR20070095949A (en) * | 2004-12-16 | 2007-10-01 | 제넨테크, 인크. | Methods for treating autoimmune disorders |
US7816320B2 (en) | 2004-12-22 | 2010-10-19 | Ambrx, Inc. | Formulations of human growth hormone comprising a non-naturally encoded amino acid at position 35 |
JP2008525032A (en) | 2004-12-22 | 2008-07-17 | アンブレツクス・インコーポレイテツド | Methods for expressing and purifying recombinant human growth hormone |
SG160437A1 (en) | 2004-12-22 | 2010-04-29 | Ambrx Inc | Modified human growth hormone |
AU2005319518B2 (en) * | 2004-12-22 | 2010-09-09 | Ambrx, Inc. | Compositions of aminoacyl-tRNA synthetase and uses thereof |
WO2006074397A2 (en) | 2005-01-05 | 2006-07-13 | Biogen Idec Ma Inc. | Cripto binding molecules |
US8029783B2 (en) * | 2005-02-02 | 2011-10-04 | Genentech, Inc. | DR5 antibodies and articles of manufacture containing same |
WO2006086242A2 (en) | 2005-02-07 | 2006-08-17 | Genenews, Inc. | Mild osteoarthritis biomarkers and uses thereof |
JP5651285B2 (en) | 2005-02-15 | 2015-01-07 | デューク ユニバーシティ | Anti-CD19 antibodies and use in oncology |
US20090142338A1 (en) * | 2005-03-04 | 2009-06-04 | Curedm, Inc. | Methods and Compositions for Treating Type 1 and Type 2 Diabetes Mellitus and Related Conditions |
EP1858545A2 (en) * | 2005-03-04 | 2007-11-28 | Curedm Inc. | Methods and pharmaceutical compositions for treating type 1 diabetes mellitus and other conditions |
CN101175769A (en) | 2005-03-10 | 2008-05-07 | 健泰科生物技术公司 | Methods and compositions for modulating vascular integrity |
AU2006227377B2 (en) | 2005-03-18 | 2013-01-31 | Medimmune, Llc | Framework-shuffling of antibodies |
GB0506912D0 (en) | 2005-04-05 | 2005-05-11 | Celltech R&D Ltd | Biological products |
AU2006236439B2 (en) | 2005-04-15 | 2012-05-03 | Macrogenics, Inc. | Covalent diabodies and uses thereof |
WO2012018687A1 (en) | 2010-08-02 | 2012-02-09 | Macrogenics, Inc. | Covalent diabodies and uses thereof |
US20060269556A1 (en) * | 2005-04-18 | 2006-11-30 | Karl Nocka | Mast cell activation using siglec 6 antibodies |
AU2006236225C1 (en) | 2005-04-19 | 2013-05-02 | Seagen Inc. | Humanized anti-CD70 binding agents and uses thereof |
AR054260A1 (en) * | 2005-04-26 | 2007-06-13 | Rinat Neuroscience Corp | METHODS OF TREATMENT OF DISEASES OF THE LOWER MOTOR NEURONE AND COMPOSITIONS USED IN THE SAME |
UY29504A1 (en) | 2005-04-29 | 2006-10-31 | Rinat Neuroscience Corp | DIRECTED ANTIBODIES AGAINST BETA AMYLOID PEPTIDE AND METHODS USING THE SAME. |
PA8672101A1 (en) | 2005-04-29 | 2006-12-07 | Centocor Inc | ANTI-IL-6 ANTIBODIES, COMPOSITIONS, METHODS AND USES |
EP2295066B1 (en) * | 2005-05-25 | 2016-04-27 | CureDM Group Holdings, LLC | Peptides, derivatives and analogs thereof, and methods of using same |
CA2609205A1 (en) * | 2005-06-03 | 2006-12-14 | Ambrx, Inc. | Improved human interferon molecules and their uses |
NZ563341A (en) | 2005-06-06 | 2009-10-30 | Genentech Inc | Methods for identifying agents that modulate a gene that encodes for a PRO1568 polypeptide |
WO2006135886A2 (en) * | 2005-06-13 | 2006-12-21 | The Regents Of The University Of Michigan | Compositions and methods for treating and diagnosing cancer |
KR20080025174A (en) | 2005-06-23 | 2008-03-19 | 메디뮨 인코포레이티드 | Antibody formulations having optimized aggregation and fragmentation profiles |
US7491391B2 (en) | 2005-06-30 | 2009-02-17 | Centocor, Inc. | Anti-IL-23 antibodies, compositions, methods and uses |
PT1904104E (en) | 2005-07-08 | 2013-11-21 | Biogen Idec Inc | Sp35 antibodies and uses thereof |
EP1904652A2 (en) * | 2005-07-08 | 2008-04-02 | Brystol-Myers Squibb Company | Single nucleotide polymorphisms associated with dose-dependent edema and methods of use thereof |
CN101282994B (en) * | 2005-07-22 | 2013-09-18 | Y's治疗有限公司 | Anti-CD26 antibodies and methods of use thereof |
EP1920057A4 (en) | 2005-08-03 | 2009-03-18 | Grains Res & Dev Corp | Polysaccharide synthases |
EP1995321A2 (en) | 2005-08-15 | 2008-11-26 | Genentech, Inc. | Gene disruptions, compositions and methods relating thereto |
US7632823B2 (en) | 2005-08-18 | 2009-12-15 | Ambrx, Inc. | Compositions of tRNA and uses thereof |
US20090215992A1 (en) * | 2005-08-19 | 2009-08-27 | Chengbin Wu | Dual variable domain immunoglobulin and uses thereof |
US20070202512A1 (en) * | 2005-08-19 | 2007-08-30 | Bristol-Myers Squibb Company | Human single nucleotide polymorphisms associated with dose-dependent weight gain and methods of use thereof |
ATE546160T1 (en) * | 2005-09-14 | 2012-03-15 | Ucb Pharma Sa | ANTIBODY COMB POLYMER CONJUGATE |
KR101176830B1 (en) | 2005-10-17 | 2012-08-27 | 주식회사 아이지세라피 | Novel method for phage display |
US8249814B2 (en) | 2005-10-21 | 2012-08-21 | Genenews Inc. | Method, computer readable medium, and system for determining a probability of colorectal cancer in a test subject |
US7723477B2 (en) | 2005-10-31 | 2010-05-25 | Oncomed Pharmaceuticals, Inc. | Compositions and methods for inhibiting Wnt-dependent solid tumor cell growth |
JP2009513708A (en) | 2005-10-31 | 2009-04-02 | オンコメッド ファーマシューティカルズ インコーポレイテッド | Compositions and methods for diagnosis and treatment of cancer |
AU2006308847C1 (en) * | 2005-10-31 | 2012-05-10 | Oncomed Pharmaceuticals, Inc. | Compositions and methods for treating and diagnosing cancer |
AU2006311828B2 (en) | 2005-11-04 | 2013-07-11 | Biogen Ma Inc. | Methods for promoting neurite outgrowth and survival of dopaminergic neurons |
AU2006311661B2 (en) | 2005-11-07 | 2011-05-26 | The Scripps Research Institute | Compositions and methods for controlling tissue factor signaling specificity |
ES2577292T3 (en) | 2005-11-07 | 2016-07-14 | Genentech, Inc. | Binding polypeptides with diversified VH / VL hypervariable sequences and consensus |
CN101400646A (en) * | 2005-11-08 | 2009-04-01 | Ambrx公司 | Accelerants for the modification of non-natural amino acids and non-natural amino acid polypeptides |
UA96139C2 (en) | 2005-11-08 | 2011-10-10 | Дженентек, Інк. | Anti-neuropilin-1 (nrp1) antibody |
KR20080068062A (en) | 2005-11-14 | 2008-07-22 | 리나트 뉴로사이언스 코퍼레이션 | Antagonist antibodies directed against calcitonin gene-related peptide and methods using same |
EP1951890A4 (en) | 2005-11-16 | 2009-06-24 | Ambrx Inc | Methods and compositions comprising non-natural amino acids |
US20090293137A1 (en) | 2005-11-21 | 2009-11-26 | Genentech, Inc. | Novel Gene Disruptions, Compositions and Methods Relating Thereto |
DK1963369T3 (en) | 2005-11-28 | 2013-06-03 | Zymogenetics Inc | IL-21 Antagonists |
CA2631181A1 (en) | 2005-12-02 | 2007-06-07 | Biogen Idec Ma Inc. | Treatment of conditions involving demyelination |
WO2007126439A2 (en) | 2005-12-02 | 2007-11-08 | Genentech, Inc. | Compositions and methods for the treatment of diseases and disorders associated with cytokine signaling involving antibodies that bind to il-22 and il-22r |
WO2007064919A2 (en) * | 2005-12-02 | 2007-06-07 | Genentech, Inc. | Binding polypeptides with restricted diversity sequences |
SI1960430T1 (en) * | 2005-12-09 | 2015-01-30 | Ucb Pharma, S.A. | Antibody molecules having specificity for human il-6 |
NZ568578A (en) * | 2005-12-14 | 2011-10-28 | Ambrx Inc | Compositions containing, methods involving, and uses of non-natural amino acids and polypeptides |
CA2635692C (en) | 2005-12-29 | 2013-06-18 | Centocor, Inc. | Human anti-il-23 antibodies, compositions, methods and uses |
SG10201400426XA (en) | 2006-01-12 | 2014-07-30 | Alexion Pharma Inc | Antibodies to ox-2/cd200 and uses thereof |
EP1987361A4 (en) * | 2006-01-30 | 2009-03-04 | Invitrogen Corp | Compositions and methods for detecting and quantifying toxic substances in disease states |
US20070175313A1 (en) * | 2006-01-31 | 2007-08-02 | Kevin Vandervliet | MP3 player holder assembly |
ZA200807714B (en) | 2006-02-17 | 2010-01-27 | Genentech Inc | Gene disruptions, compositions and methods relating thereto |
AU2007218045B2 (en) * | 2006-02-20 | 2011-11-10 | Phylogica Limited | Method of constructing and screening libraries of peptide structures |
US20070243192A1 (en) * | 2006-02-21 | 2007-10-18 | Regents Of The University Of Michigan | Growth hormone receptor antagonist cancer treatment |
WO2008121102A2 (en) * | 2006-02-21 | 2008-10-09 | The Regents Of The University Of Michigan | Hedgehog signaling pathway antagonist cancer treatment |
US8021839B2 (en) * | 2006-02-24 | 2011-09-20 | Investigen, Inc. | Methods and compositions for detecting polynucleotides |
WO2007103469A2 (en) | 2006-03-06 | 2007-09-13 | Aeres Biomedical Ltd. | Humanized anti-cd22 antibodies and their use in treatment of oncology, transplantation and autoimmune disease |
CA2647277A1 (en) | 2006-04-05 | 2007-11-08 | Genentech, Inc. | Method for using boc/cdo to modulate hedgehog signaling |
AU2007238186B2 (en) | 2006-04-10 | 2014-01-09 | Genentech, Inc. | Disheveled PDZ modulators |
EP2082645A1 (en) | 2006-04-19 | 2009-07-29 | Genentech, Inc. | Novel gene disruptions, compositions and methods relating thereto |
TW200812616A (en) * | 2006-05-09 | 2008-03-16 | Genentech Inc | Binding polypeptides with optimized scaffolds |
US20090142259A1 (en) * | 2006-05-12 | 2009-06-04 | Genentech, Inc. | Compositions and methods for the diagnosis and treatment of bladder and urinary tract tumors |
US7862812B2 (en) | 2006-05-31 | 2011-01-04 | Lpath, Inc. | Methods for decreasing immune response and treating immune conditions |
GB0611116D0 (en) | 2006-06-06 | 2006-07-19 | Oxford Genome Sciences Uk Ltd | Proteins |
ES2718952T3 (en) | 2006-06-07 | 2019-07-05 | Bioalliance Cv | Antibodies that recognize an epitope that contains carbohydrates on CD-43 and CEA expressed in cancer cells and methods that use them |
SG10201504662WA (en) | 2006-06-14 | 2015-07-30 | Macrogenics Inc | Methods For The Treatment Of Autoimmune Disorders Using Immunosuppressive Monoclonal Antibodies With Reduced Toxicity |
EP2505209A1 (en) | 2006-06-26 | 2012-10-03 | MacroGenics, Inc. | Fcgamma-RIIB-specific antibodies and methods of the use thereof |
DE102006030028A1 (en) * | 2006-06-29 | 2008-02-14 | Forschungszentrum Jülich GmbH | A method for finding bait-binding specific molecules and bait-binding molecules and their use |
US7572618B2 (en) | 2006-06-30 | 2009-08-11 | Bristol-Myers Squibb Company | Polynucleotides encoding novel PCSK9 variants |
KR101528939B1 (en) * | 2006-07-18 | 2015-06-15 | 사노피 | Antagonist antibody against epha2 for the treatment of cancer |
EP2057465A4 (en) | 2006-08-09 | 2010-04-21 | Homestead Clinical Corp | Organ-specific proteins and methods of their use |
MY162024A (en) | 2006-08-28 | 2017-05-31 | La Jolla Inst Allergy & Immunology | Antagonistic human light-specific human monoclonal antibodies |
CA2662629C (en) | 2006-09-07 | 2019-08-13 | University Of Otago | Bnp signal peptide fragments for acute cardiac disorders |
NZ574960A (en) * | 2006-09-08 | 2012-02-24 | Ambrx Inc | Suppressor trna transcription in vertebrate cells |
PT2061878E (en) * | 2006-09-08 | 2014-04-22 | Ambrx Inc | Hybrid suppressor trna for vertebrate cells |
WO2008030558A2 (en) * | 2006-09-08 | 2008-03-13 | Ambrx, Inc. | Modified human plasma polypeptide or fc scaffolds and their uses |
CA2662236A1 (en) | 2006-09-12 | 2008-03-20 | Genentech, Inc. | Methods and compositions for the diagnosis and treatment of cancer |
EP2074138A4 (en) * | 2006-09-19 | 2009-12-30 | Phylogica Ltd | Neuroprotective peptide inhibitors of ap-1 signaling and uses therefor |
DK2066694T3 (en) | 2006-09-29 | 2016-02-08 | Oncomed Pharm Inc | Compositions and Methods for Diagnosing and Treating Cancer |
JP5298021B2 (en) * | 2006-10-12 | 2013-09-25 | ジェネンテック, インコーポレイテッド | Antibodies against lymphotoxin-α |
US20100143254A1 (en) | 2006-10-16 | 2010-06-10 | Medimmune, Llc | Molecules with reduced half-lives, compositions and uses thereof |
GB0620729D0 (en) | 2006-10-18 | 2006-11-29 | Ucb Sa | Biological products |
EP1914242A1 (en) | 2006-10-19 | 2008-04-23 | Sanofi-Aventis | Novel anti-CD38 antibodies for the treatment of cancer |
US20080096193A1 (en) * | 2006-10-24 | 2008-04-24 | Charles Robert Bupp | Methods and compositions for detecting polynucleotides |
WO2008054821A2 (en) | 2006-10-30 | 2008-05-08 | Promega Corporation | Mutant hydrolase proteins with enhanced kinetics and functional expression |
US8785400B2 (en) * | 2006-11-22 | 2014-07-22 | Curedm Group Holdings, Llc | Methods and compositions relating to islet cell neogenesis |
CA2671264C (en) * | 2006-11-30 | 2015-11-24 | Research Development Foundation | Improved immunoglobulin libraries |
ES2523915T5 (en) | 2006-12-01 | 2022-05-26 | Seagen Inc | Variant Target Binding Agents and Uses Thereof |
EP2687232A1 (en) | 2006-12-06 | 2014-01-22 | MedImmune, LLC | Methods of treating systemic lupus erythematosus |
KR20140031996A (en) | 2006-12-19 | 2014-03-13 | 제넨테크, 인크. | Vegf-specific antagonists for adjuvant and neoadjuvant therapy and the treatment of early stage tumors |
EP2913341A1 (en) | 2006-12-22 | 2015-09-02 | University of Utah Research Foundation | Method of detecting ocular diseases and pathologic conditions and treatment of same |
US20090068110A1 (en) * | 2006-12-22 | 2009-03-12 | Genentech, Inc. | Antibodies to insulin-like growth factor receptor |
US8128926B2 (en) | 2007-01-09 | 2012-03-06 | Biogen Idec Ma Inc. | Sp35 antibodies and uses thereof |
UA99120C2 (en) | 2007-01-09 | 2012-07-25 | Байоджэн Айдэк Ма Инк. | Sp35 antibodies and uses thereof |
WO2008092002A2 (en) | 2007-01-24 | 2008-07-31 | The Regents Of The University Of Michigan | Compositions and methods for treating and diagnosing pancreatic cancer |
EP2629094A1 (en) | 2007-01-24 | 2013-08-21 | Carnegie Mellon University | Optical biosensors |
CN101652389A (en) | 2007-02-09 | 2010-02-17 | 健泰科生物技术公司 | Anti-ROBO4 antibodies and uses therefor |
US8114606B2 (en) * | 2007-02-16 | 2012-02-14 | The Board Of Trustees Of Southern Illinois University | ARL-1 specific antibodies |
US8685666B2 (en) * | 2007-02-16 | 2014-04-01 | The Board Of Trustees Of Southern Illinois University | ARL-1 specific antibodies and uses thereof |
KR101508397B1 (en) | 2007-02-22 | 2015-04-08 | 제넨테크, 인크. | Methods for detecting inflammatory bowel disease |
WO2008103702A2 (en) * | 2007-02-23 | 2008-08-28 | Investigen, Inc. | Methods and compositions for rapid light-activated isolation and detection of analytes |
EP3118221B1 (en) | 2007-02-26 | 2019-08-21 | Oxford BioTherapeutics Ltd | Proteins |
WO2008104803A2 (en) | 2007-02-26 | 2008-09-04 | Oxford Genome Sciences (Uk) Limited | Proteins |
EP2124952A2 (en) | 2007-02-27 | 2009-12-02 | Abbott GmbH & Co. KG | Method for the treatment of amyloidoses |
SI2125894T1 (en) | 2007-03-22 | 2019-05-31 | Biogen Ma Inc. | Binding proteins, including antibodies, antibody derivatives and antibody fragments, that specifically bind cd154 and uses thereof |
JP5456658B2 (en) | 2007-03-30 | 2014-04-02 | メディミューン,エルエルシー | Antibody preparation |
CA2682147C (en) * | 2007-03-30 | 2017-08-08 | Ambrx, Inc. | Modified fgf-21 polypeptides and their uses |
US20100291562A1 (en) * | 2007-04-04 | 2010-11-18 | Michael Adler | Method for the detection of an analyte in biological matrix |
US7807168B2 (en) * | 2007-04-10 | 2010-10-05 | Vaccinex, Inc. | Selection of human TNFα specific antibodies |
BRPI0810622A2 (en) | 2007-05-02 | 2020-10-13 | Ambrx, Inc. | modified interferon beta polypeptides and their uses |
SG194368A1 (en) | 2007-05-04 | 2013-11-29 | Technophage Investigacao E Desenvolvimento Em Biotecnologia Sa | Engineered rabbit antibody variable domains and uses thereof |
EP2703011A3 (en) | 2007-05-07 | 2014-03-26 | MedImmune, LLC | Anti-icos antibodies and their use in treatment of oncology, transplantation and autoimmune disease |
CN103223167B (en) | 2007-05-14 | 2015-06-17 | 米迪缪尼有限公司 | Methods of reducing eosinophil levels |
AU2007353779B2 (en) * | 2007-05-17 | 2013-11-07 | Genentech, Inc. | Crystal structures of neuropilin fragments and neuropilin-antibody complexes |
US7906149B2 (en) * | 2007-05-25 | 2011-03-15 | Boval Company, L.P. | Method for treating allergic dermatitis |
US20090232801A1 (en) * | 2007-05-30 | 2009-09-17 | Abbot Laboratories | Humanized Antibodies Which Bind To AB (1-42) Globulomer And Uses Thereof |
PE20090329A1 (en) * | 2007-05-30 | 2009-03-27 | Abbott Lab | HUMANIZED ANTIBODIES AGAINST GLOBULOMER AB (20-42) AND ITS USES |
WO2008154700A1 (en) * | 2007-06-20 | 2008-12-24 | Phylogica Limited | Compositions and uses thereof for the treatment of acute respiratory distress syndrome (ards) and clinical disorders associated with therewith |
KR101799337B1 (en) | 2007-06-21 | 2017-12-20 | 마크로제닉스, 인크. | Covalent diabodies and uses thereof |
PT2173379E (en) | 2007-07-02 | 2015-11-24 | Oncomed Pharm Inc | Compositions and methods for treating and diagnosing cancer |
JP2010534664A (en) | 2007-07-23 | 2010-11-11 | セントコア・オーソ・バイオテツク・インコーポレーテツド | Methods and compositions for treatment of fibrosis related diseases using IL-17 antagonists |
BRPI0814645A2 (en) * | 2007-07-25 | 2015-01-27 | Alexion Pharma Inc | METHODS AND COMPOSITIONS FOR TREATING AUTOIMMUNE DISEASE. |
WO2009020477A1 (en) * | 2007-08-06 | 2009-02-12 | Yale University | Modified miniature proteins |
ES2534434T3 (en) * | 2007-08-30 | 2015-04-22 | Curedm Group Holdings, Llc | Compositions and methods of using proislot peptides and analogs thereof |
GB0717337D0 (en) | 2007-09-06 | 2007-10-17 | Ucb Pharma Sa | Method of treatment |
JP5933894B2 (en) | 2007-09-14 | 2016-06-15 | アディマブ, エルエルシー | Rationally designed synthetic antibody libraries and their use |
US8877688B2 (en) * | 2007-09-14 | 2014-11-04 | Adimab, Llc | Rationally designed, synthetic antibody libraries and uses therefor |
TWI464262B (en) | 2007-09-26 | 2014-12-11 | 中外製藥股份有限公司 | Antibody constant region mutant |
CA2700714C (en) | 2007-09-26 | 2018-09-11 | Ucb Pharma S.A. | Dual specificity antibody fusions |
NZ584330A (en) * | 2007-10-04 | 2013-01-25 | Bionomics Ltd | Markers of endothelial cells and uses thereof |
RU2530561C2 (en) | 2007-11-05 | 2014-10-10 | Медиммун, Ллк | Method of treating scleroderma |
RU2503460C2 (en) | 2007-11-07 | 2014-01-10 | Дженентек Инк. | Using antimicrobial polypeptide for treating microbial disorders |
JP5580205B2 (en) | 2007-11-19 | 2014-08-27 | セレラ コーポレーション | Lung cancer markers and their use |
JP5547083B2 (en) | 2007-11-20 | 2014-07-09 | アンブルックス,インコーポレイテッド | Modified insulin polypeptides and their use |
WO2009070642A1 (en) * | 2007-11-28 | 2009-06-04 | Medimmune, Llc | Protein formulation |
US8426153B2 (en) | 2007-12-03 | 2013-04-23 | Carnegie Mellon University | Linked peptides fluorogenic biosensors |
RU2570559C2 (en) | 2007-12-17 | 2015-12-10 | Пфайзер Лимитед | Treatment of interstitial cystitis |
CA2706502C (en) | 2007-12-18 | 2018-08-07 | Bioalliance C.V. | Antibodies recognizing a carbohydrate containing epitope on cd-43 and cea expressed on cancer cells and methods using same |
CN101932333A (en) | 2007-12-26 | 2010-12-29 | 瓦西尼斯公司 | Anti-c 35 antibody combination therapies and method |
GB0800277D0 (en) | 2008-01-08 | 2008-02-13 | Imagination Tech Ltd | Video motion compensation |
US8821863B2 (en) | 2008-01-11 | 2014-09-02 | Gene Techno Science Co., Ltd. | Humanized anti-α 9 integrin antibodies and the uses thereof |
BRPI0907046A2 (en) | 2008-01-18 | 2015-07-28 | Medimmune Llc | Engineered cysteine antibody, isolated nucleic acid, vector, host cell, antibody conjugate, pharmaceutical composition, methods of detecting cancer, autoimmune, inflammatory or infectious disorders in an individual and inhibiting proliferation of a target cell |
MX2010008632A (en) | 2008-02-08 | 2010-08-30 | Ambrx Inc | Modified leptin polypeptides and their uses. |
AU2009212273B2 (en) | 2008-02-08 | 2014-07-31 | Astrazeneca Ab | Anti-IFNAR1 antibodies with reduced Fc ligand affinity |
CN107296957A (en) | 2008-03-04 | 2017-10-27 | 梯瓦制药国际有限责任公司 | The method for treating chronic ache |
MX2010009724A (en) | 2008-03-04 | 2010-09-28 | Pfizer Ltd | Methods of treating inflammatory pain. |
WO2009111644A2 (en) * | 2008-03-05 | 2009-09-11 | The Regents Of The University Of Michigan | Compositions and methods for diagnosing and treating pancreatic cancer |
AU2009224113B2 (en) * | 2008-03-12 | 2013-02-21 | Otago Innovation Limited | Biomarkers |
US8507209B2 (en) | 2008-03-12 | 2013-08-13 | Otago Innovation Limited | Biomarkers |
WO2009114815A1 (en) | 2008-03-13 | 2009-09-17 | Dyax Corp | Libraries of genetic packages comprising novel hc cdr3 designs |
US20110020368A1 (en) | 2008-03-25 | 2011-01-27 | Nancy Hynes | Treating cancer by down-regulating frizzled-4 and/or frizzled-1 |
EP2271770B1 (en) * | 2008-03-31 | 2018-08-22 | Genentech, Inc. | Compositions and methods for treating and diagnosing asthma |
AU2009231991B2 (en) | 2008-04-02 | 2014-09-25 | Macrogenics, Inc. | HER2/neu-specific antibodies and methods of using same |
EP2252631B1 (en) | 2008-04-02 | 2016-04-13 | MacroGenics, Inc. | Bcr-complex-specific antibodies and methods of using same |
WO2009126934A2 (en) | 2008-04-11 | 2009-10-15 | Seattle Genetics, Inc. | Detection and tratment of pancreatic, ovarian and other cancers |
GB0807413D0 (en) | 2008-04-23 | 2008-05-28 | Ucb Pharma Sa | Biological products |
WO2009132287A2 (en) * | 2008-04-24 | 2009-10-29 | Dyax Corp. | Libraries of genetic packages comprising novel hc cdr1, cdr2, and cdr3 and novel lc cdr1, cdr2, and cdr3 designs |
AU2009238897B2 (en) | 2008-04-24 | 2015-03-19 | Gene Techno Science Co., Ltd. | Humanized antibodies specific for amino acid sequence RGD of an extracellular matrix protein and the uses thereof |
US20090269786A1 (en) * | 2008-04-25 | 2009-10-29 | The Board Of Trustees Of The University Of Illinois | RHO1-Gamma Amino Butyric Acid C Receptor-Specific Antibodies |
PL2282773T3 (en) | 2008-05-02 | 2014-08-29 | Seattle Genetics Inc | Methods and compositions for making antibodies and antibody derivatives with reduced core fucosylation |
ES2605471T3 (en) | 2008-05-06 | 2017-03-14 | Genentech, Inc. | Variants of matured affinity CRIg |
SI2279004T1 (en) * | 2008-05-16 | 2015-05-29 | F. Hoffmann-La Roche Ag | Use of biomarkers for assessing treatment of gastrointestinal inflammatory disorders with beta7integrin antagonists |
US8093018B2 (en) | 2008-05-20 | 2012-01-10 | Otsuka Pharmaceutical Co., Ltd. | Antibody identifying an antigen-bound antibody and an antigen-unbound antibody, and method for preparing the same |
WO2009148896A2 (en) | 2008-05-29 | 2009-12-10 | Nuclea Biotechnologies, LLC | Anti-phospho-akt antibodies |
WO2010033279A2 (en) | 2008-06-04 | 2010-03-25 | Macrogenics, Inc. | Antibodies with altered binding to fcrn and methods of using same |
WO2009150623A1 (en) | 2008-06-13 | 2009-12-17 | Pfizer Inc | Treatment of chronic prostatitis |
JP5560270B2 (en) | 2008-07-08 | 2014-07-23 | オンコメッド ファーマシューティカルズ インコーポレイテッド | NOTCH binding agents and antagonists and methods of use thereof |
NZ591235A (en) * | 2008-07-23 | 2012-07-27 | Ambrx Inc | Modified bovine g-csf polypeptides comprising non natural amino acid and their uses treating infections such as mastitis |
US9182406B2 (en) * | 2008-08-04 | 2015-11-10 | Biodesy, Inc. | Nonlinear optical detection of molecules comprising an unnatural amino acid possessing a hyperpolarizability |
US8652843B2 (en) | 2008-08-12 | 2014-02-18 | Oncomed Pharmaceuticals, Inc. | DDR1-binding agents and methods of use thereof |
EA026110B1 (en) | 2008-08-14 | 2017-03-31 | Сефалон Острэйлиа Пти Лтд. | Anti-il-12/il-23 antibodies |
TWI445716B (en) | 2008-09-12 | 2014-07-21 | Rinat Neuroscience Corp | Pcsk9 antagonists |
US20100081575A1 (en) * | 2008-09-22 | 2010-04-01 | Robert Anthony Williamson | Methods for creating diversity in libraries and libraries, display vectors and methods, and displayed molecules |
AU2009293640A1 (en) * | 2008-09-22 | 2010-03-25 | Calmune Corporation | Methods and vectors for display of 2G12 -derived domain exchanged antibodies |
NO2337846T3 (en) | 2008-09-26 | 2018-06-16 | ||
BRPI0919473A2 (en) | 2008-09-26 | 2017-08-29 | Oncomed Pharm Inc | FRIZZLED BINDING AGENTS AND THEIR USES |
NZ592250A (en) | 2008-09-26 | 2012-11-30 | Lilly Co Eli | Modified animal erythropoietin polypeptides and their uses |
WO2010047515A2 (en) | 2008-10-20 | 2010-04-29 | 광주과학기술원 | Bipodal peptide binder |
US20120251502A1 (en) | 2008-10-24 | 2012-10-04 | The Government of the US as Represented by the Secretary of the Dept. of health | Human Ebola Virus Species and Compositions and Methods Thereof |
JP5848607B2 (en) | 2008-10-31 | 2016-01-27 | ヤンセン バイオテツク,インコーポレーテツド | Scaffold compositions, methods and uses based on fibronectin type 3 domains |
US9221902B2 (en) | 2008-11-07 | 2015-12-29 | Fabrus, Inc. | Combinatorial antibody libraries and uses thereof |
DK2894165T3 (en) | 2008-11-10 | 2023-03-20 | Alexion Pharma Inc | Methods and compositions for treating complement-related disorders |
SI2356462T1 (en) | 2008-11-11 | 2017-05-31 | The Regents Of The University Of Michigan | Anti-cxcr1 compositions and methods |
CN102438652B (en) | 2008-11-12 | 2014-08-13 | 米迪缪尼有限公司 | Antibody formulation |
ATE523603T1 (en) * | 2008-11-21 | 2011-09-15 | Chimera Biotec Gmbh | CONJUGATE COMPLEXES FOR ANALYTE DETECTION |
DK2752189T3 (en) | 2008-11-22 | 2017-01-16 | Hoffmann La Roche | APPLICATION OF ANTI-VEGF ANTIBODY IN COMBINATION WITH CHEMOTHERY TO TREAT CANCER CANCER |
NZ593314A (en) * | 2008-12-04 | 2013-03-28 | Abbott Lab | Dual variable domain immunoglobulins and uses thereof |
CA2740806C (en) | 2008-12-09 | 2021-07-20 | Bryan Irving | Anti-pd-l1 antibodies and their use to enhance t-cell function |
MX2011006416A (en) | 2008-12-19 | 2011-07-12 | Macrogenics Inc | Covalent diabodies and uses thereof. |
BRPI0918211A2 (en) | 2008-12-23 | 2015-12-08 | Genentech Inc | patient identification methods, patient responsiveness prediction methods, monitoring methods, therapeutic efficacy optimization methods, and p1gf expression level detection kit |
AU2009334498A1 (en) | 2008-12-31 | 2011-07-21 | Biogen Idec Ma Inc. | Anti-lymphotoxin antibodies |
GB0900425D0 (en) | 2009-01-12 | 2009-02-11 | Ucb Pharma Sa | Biological products |
WO2010082134A1 (en) | 2009-01-14 | 2010-07-22 | Iq Therapeutics Bv | Combination antibodies for the treatment and prevention of disease caused by bacillus anthracis and related bacteria and their toxins |
WO2010085510A1 (en) | 2009-01-20 | 2010-07-29 | Zadeh Homayoun H | Antibody mediated osseous regeneration |
AU2010207552A1 (en) | 2009-01-21 | 2011-09-01 | Oxford Biotherapeutics Ltd. | PTA089 protein |
WO2010088393A2 (en) * | 2009-01-28 | 2010-08-05 | Antigen Express, Inc. | Li-kay hybrid peptides that modulate the immune response to influenza |
US20110165063A1 (en) * | 2009-01-29 | 2011-07-07 | Abbott Laboratories | Il-1 binding proteins |
WO2010087927A2 (en) | 2009-02-02 | 2010-08-05 | Medimmune, Llc | Antibodies against and methods for producing vaccines for respiratory syncytial virus |
WO2010086828A2 (en) | 2009-02-02 | 2010-08-05 | Rinat Neuroscience Corporation | Agonist anti-trkb monoclonal antibodies |
WO2010093993A2 (en) | 2009-02-12 | 2010-08-19 | Human Genome Sciences, Inc. | Use of b lymphocyte stimulator protein antagonists to promote transplantation tolerance |
CN102596992B (en) | 2009-02-12 | 2015-09-09 | 詹森生物科技公司 | Based on the holder combination thing of III type fibronectin domain, method and purposes |
AR075504A1 (en) | 2009-02-17 | 2011-04-06 | Ucb Pharma Sa | MOLECULES OF ANTIBODIES THAT HAVE SPECIFICITY FOR THE HUMAN OX40 |
EP2398860B1 (en) | 2009-02-18 | 2013-11-20 | Carnegie Mellon University | Quenched dendrimeric dyes for fluorescence detection |
US20110311521A1 (en) | 2009-03-06 | 2011-12-22 | Pico Caroni | Novel therapy for anxiety |
EP2406285B1 (en) | 2009-03-10 | 2016-03-09 | Gene Techno Science Co., Ltd. | Generation, expression and characterization of the humanized k33n monoclonal antibody |
GB0904214D0 (en) | 2009-03-11 | 2009-04-22 | Ucb Pharma Sa | Biological products |
KR101523127B1 (en) | 2009-03-25 | 2015-05-26 | 제넨테크, 인크. | Novel anti-alpha5beta1 antibodies and uses thereof |
EP2241323A1 (en) | 2009-04-14 | 2010-10-20 | Novartis Forschungsstiftung, Zweigniederlassung Friedrich Miescher Institute For Biomedical Research | Tenascin-W and brain cancers |
MX2011011075A (en) | 2009-04-20 | 2011-11-04 | Oxford Biotherapeutics Ltd | Antibodies specific to cadherin-17. |
US9067986B2 (en) | 2009-04-27 | 2015-06-30 | Oncomed Pharmaceuticals, Inc. | Method for making heteromultimeric molecules |
KR101224468B1 (en) | 2009-05-20 | 2013-01-23 | 주식회사 파멥신 | Bispecific antibody having a novel form and use thereof |
CA2762837C (en) * | 2009-05-20 | 2021-08-03 | Novimmune S.A. | Synthetic polypeptide libraries and methods for generating naturally diversified polypeptide variants |
US8680055B2 (en) | 2009-06-03 | 2014-03-25 | University Of Southern California | Methods for decreasing steroidogenesis in prostate cancer cells |
US8748386B2 (en) | 2009-06-10 | 2014-06-10 | New York University | Immunological targeting of pathological Tau proteins |
WO2010146511A1 (en) | 2009-06-17 | 2010-12-23 | Pfizer Limited | Treatment of overactive bladder |
AU2010270979B2 (en) | 2009-06-22 | 2015-04-23 | Medimmune, Llc | Engineered Fc regions for site-specific conjugation |
US20110027275A1 (en) | 2009-07-31 | 2011-02-03 | Napoleone Ferrara | Inhibition of tumor metastasis |
PT2464725T (en) | 2009-08-11 | 2020-05-21 | Hoffmann La Roche | Production of proteins in glutamine-free cell culture media |
WO2011020079A1 (en) * | 2009-08-13 | 2011-02-17 | Calmune Corporation | Antibodies against human respiratory syncytial virus (rsv) and methods of use |
CN102573909A (en) | 2009-08-15 | 2012-07-11 | 霍夫曼-拉罗奇有限公司 | Anti-angiogenesis therapy for the treatment of previously treated breast cancer |
EP2292266A1 (en) | 2009-08-27 | 2011-03-09 | Novartis Forschungsstiftung, Zweigniederlassung | Treating cancer by modulating copine III |
CN102740884A (en) | 2009-08-28 | 2012-10-17 | 瑞纳神经科学公司 | Methods for treating visceral pain by administering antagonist antibodies directed against calcitonin gene-related peptide |
US20110059111A1 (en) | 2009-09-01 | 2011-03-10 | Los Angeles Biomedical Research Institute At Harbor-Ucla Medical Center | Mammalian receptors as targets for antibody and active vaccination therapy against mold infections |
WO2011030107A1 (en) | 2009-09-10 | 2011-03-17 | Ucb Pharma S.A. | Multivalent antibodies |
EP2478136A4 (en) * | 2009-09-14 | 2013-09-25 | Dyax Corp | Libraries of genetic packages comprising novel hc cdr3 designs |
MX2012002909A (en) | 2009-09-17 | 2012-04-19 | Hoffmann La Roche | Methods and compositions for diagnostics use in cancer patients. |
US20120244170A1 (en) | 2009-09-22 | 2012-09-27 | Rafal Ciosk | Treating cancer by modulating mex-3 |
GB201005063D0 (en) | 2010-03-25 | 2010-05-12 | Ucb Pharma Sa | Biological products |
AR078470A1 (en) | 2009-10-02 | 2011-11-09 | Sanofi Aventis | ANTIBODIES THAT SPECIFICALLY JOIN THE EPHA2 RECEIVER |
WO2011047083A1 (en) | 2009-10-13 | 2011-04-21 | Oxford Biotherapeutics Ltd. | Antibodies against epha10 |
WO2011045352A2 (en) | 2009-10-15 | 2011-04-21 | Novartis Forschungsstiftung | Spleen tyrosine kinase and brain cancers |
DK2488204T3 (en) | 2009-10-16 | 2016-06-06 | Oncomed Pharm Inc | Therapeutic combination and use of DLL4 antagonist antibodies and blood pressure lowering agents |
CA2778442A1 (en) | 2009-10-22 | 2011-04-28 | Genentech, Inc. | Methods and compositions for modulating hepsin activation of macrophage-stimulating protein |
GB0922434D0 (en) | 2009-12-22 | 2010-02-03 | Ucb Pharma Sa | antibodies and fragments thereof |
US9234037B2 (en) | 2009-10-27 | 2016-01-12 | Ucb Biopharma Sprl | Method to generate antibodies to ion channels |
GB0922435D0 (en) | 2009-12-22 | 2010-02-03 | Ucb Pharma Sa | Method |
US8734798B2 (en) | 2009-10-27 | 2014-05-27 | Ucb Pharma S.A. | Function modifying NAv 1.7 antibodies |
US20120213801A1 (en) | 2009-10-30 | 2012-08-23 | Ekaterina Gresko | Phosphorylated Twist1 and cancer |
US20120282177A1 (en) | 2009-11-02 | 2012-11-08 | Christian Rohlff | ROR1 as Therapeutic and Diagnostic Target |
US20120277144A1 (en) | 2009-11-04 | 2012-11-01 | Henricus Johannes Duckers | Novel compounds for modulating neovascularisation and methods of treatment using these compounds |
GB0920127D0 (en) | 2009-11-17 | 2009-12-30 | Ucb Pharma Sa | Antibodies |
GB0920324D0 (en) | 2009-11-19 | 2010-01-06 | Ucb Pharma Sa | Antibodies |
MX2012006072A (en) | 2009-11-30 | 2012-07-23 | Genentech Inc | Antibodies for treating and diagnosing tumors expressing slc34a2 (tat211 = seqid2 ). |
WO2011070443A1 (en) | 2009-12-09 | 2011-06-16 | Institut National De La Sante Et De La Recherche Medicale | Monoclonal antibodies that bind b7h6 and uses thereof |
WO2011084496A1 (en) * | 2009-12-16 | 2011-07-14 | Abbott Biotherapeutics Corp. | Anti-her2 antibodies and their uses |
CN104017063A (en) | 2009-12-21 | 2014-09-03 | Ambrx公司 | Modified porcine somatotropin polypeptides and their uses |
CN107674121A (en) | 2009-12-21 | 2018-02-09 | Ambrx 公司 | Bovine somatotropin polypeptide and its purposes by modification |
WO2011079283A1 (en) * | 2009-12-23 | 2011-06-30 | Bioalliance C.V. | Anti-epcam antibodies that induce apoptosis of cancer cells and methods using same |
US9180186B2 (en) | 2010-01-11 | 2015-11-10 | Alexion Pharmaceuticals, Inc. | Biomarkers of immunomodulatory effects in humans treated with anti-CD200 antibodies |
GB201000467D0 (en) | 2010-01-12 | 2010-02-24 | Ucb Pharma Sa | Antibodies |
TWI535445B (en) | 2010-01-12 | 2016-06-01 | 安可美德藥物股份有限公司 | Wnt antagonists and methods of treatment and screening |
CN102958534B (en) | 2010-01-13 | 2014-11-05 | 昂考梅德药品有限公司 | Notch1 binding agents and methods of use thereof |
CA2789629A1 (en) | 2010-02-10 | 2011-08-18 | Immunogen, Inc. | Cd20 antibodies and uses thereof |
US10393754B2 (en) | 2010-02-17 | 2019-08-27 | Cedars-Sinai Medical Center | Methods of diagnosing and treating heart failure |
SG183333A1 (en) | 2010-02-18 | 2012-09-27 | Genentech Inc | Neuregulin antagonists and use thereof in treating cancer |
US20110200595A1 (en) | 2010-02-18 | 2011-08-18 | Roche Glycart | TREATMENT WITH A HUMANIZED IgG CLASS ANTI EGFR ANTIBODY AND AN ANTIBODY AGAINST INSULIN LIKE GROWTH FACTOR 1 RECEPTOR |
BR112012020373A8 (en) | 2010-02-23 | 2018-01-02 | Genentech Inc | isolated antibody, cell, isolated nucleic acid, method of identification, cell proliferation inhibition, therapeutic treatment, determination of the presence of a tat419 protein, diagnosis of the presence of cancer and distribution of cytotoxic agent |
KR101839161B1 (en) | 2010-02-23 | 2018-03-16 | 제넨테크, 인크. | Anti-angiogenesis therapy for the treatment of ovarian cancer |
SA114360064B1 (en) | 2010-02-24 | 2016-01-05 | رينات نيوروساينس كوربوريشن | Antagonist anti-il-7 receptor antibodies and methods |
TWI672318B (en) | 2010-02-24 | 2019-09-21 | 美商免疫遺傳股份有限公司 | Folate receptor 1 antibodies and immunoconjugates and uses thereof |
US20130004519A1 (en) | 2010-03-05 | 2013-01-03 | Ruth Chiquet-Ehrismann | Smoci, tenascin-c and brain cancers |
AU2011225716A1 (en) | 2010-03-11 | 2012-09-27 | Pfizer Inc. | Antibodies with pH dependent antigen binding |
EP2544719B1 (en) | 2010-03-12 | 2019-07-03 | Debiopharm International S.A. | Cd37-binding molecules and immunoconjugates thereof |
EP2547359B1 (en) | 2010-03-15 | 2016-03-09 | The Board of Trustees of the University of Illionis | Inhibitors of beta integrin-g protein alpha subunit binding interactions |
EP2548030B1 (en) * | 2010-03-18 | 2015-05-27 | Cornell University | Engineering correctly folded antibodies using inner membrane display of twin-arginine translocation intermediates |
BR112012022044A2 (en) | 2010-03-24 | 2020-08-25 | Genentech Inc | ''antibody, immunoconjugate, pharmaceutical formulation, antibody use, treatment method, isolated bispecific antibody and host cell''. |
WO2011117653A1 (en) | 2010-03-25 | 2011-09-29 | Ucb Pharma S.A. | Disulfide stabilized dvd-lg molecules |
GB201005064D0 (en) | 2010-03-25 | 2010-05-12 | Ucb Pharma Sa | Biological products |
CA2793959C (en) | 2010-03-25 | 2019-06-04 | Oregon Health & Science University | Cmv glycoproteins and recombinant vectors |
CA2794674A1 (en) | 2010-04-01 | 2011-10-06 | Oncomed Pharmaceuticals, Inc. | Frizzled-binding agents and uses thereof |
EP2561076A1 (en) | 2010-04-19 | 2013-02-27 | Novartis Forschungsstiftung, Zweigniederlassung Friedrich Miescher Institute For Biomedical Research | Modulating xrn1 |
EP2380909A1 (en) | 2010-04-26 | 2011-10-26 | Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. | PTK-7 protein involved in breast cancer |
ES2552954T3 (en) | 2010-04-30 | 2015-12-03 | Alexion Pharmaceuticals, Inc. | Anti-C5a antibodies and methods for the use of antibodies |
CN102958941A (en) | 2010-05-03 | 2013-03-06 | 霍夫曼-拉罗奇有限公司 | Compositions and methods for the diagnosis and treatment of tumor |
ES2606017T3 (en) | 2010-05-03 | 2017-03-17 | University Of Rochester | Passive anti-glucosaminidase immunization for Staphylococcus aureus infections |
EP2569335B1 (en) | 2010-05-14 | 2018-08-22 | Orega Biotech | Methods of treating and/or preventing cell proliferation disorders with il-17 antagonists |
EP2577309B1 (en) | 2010-05-25 | 2016-11-23 | Carnegie Mellon University | Targeted probes of cellular physiology |
WO2011153243A2 (en) | 2010-06-02 | 2011-12-08 | Genentech, Inc. | Anti-angiogenesis therapy for treating gastric cancer |
US20130089538A1 (en) | 2010-06-10 | 2013-04-11 | Novartis Forschungsstiftung, Zweigniederlassung Friedrich Miescher Institute forBiomedical Researh | Treating cancer by modulating mammalian sterile 20-like kinase 3 |
CA2794731C (en) | 2010-06-18 | 2019-03-19 | Genentech, Inc. | Anti-axl antibodies and methods of use |
NZ603488A (en) | 2010-07-09 | 2015-02-27 | Crucell Holland Bv | Anti-human respiratory syncytial virus (rsv) antibodies and methods of use |
WO2012006633A1 (en) | 2010-07-09 | 2012-01-12 | Biogen Idec Hemophilia Inc. | Chimeric clotting factors |
KR20130120439A (en) | 2010-07-09 | 2013-11-04 | 제넨테크, 인크. | Anti-neuropilin antibodies and methods of use |
WO2012009705A1 (en) | 2010-07-15 | 2012-01-19 | Zyngenia, Inc. | Ang-2 binding complexes and uses thereof |
US9354228B2 (en) | 2010-07-16 | 2016-05-31 | Adimab, Llc | Antibody libraries |
WO2012012469A2 (en) | 2010-07-19 | 2012-01-26 | Otago Innovation Limited | Signal biomarkers |
WO2012010582A1 (en) | 2010-07-21 | 2012-01-26 | Roche Glycart Ag | Anti-cxcr5 antibodies and methods of use |
WO2012012750A1 (en) | 2010-07-23 | 2012-01-26 | Trustees Of Boston University | ANTI-DEsupR INHIBITORS AS THERAPEUTICS FOR INHIBITION OF PATHOLOGICAL ANGIOGENESIS AND TUMOR CELL INVASIVENESS AND FOR MOLECULAR IMAGING AND TARGETED DELIVERY |
WO2012015758A2 (en) | 2010-07-30 | 2012-02-02 | Saint Louis University | Methods of treating pain |
CN103153341B (en) | 2010-08-03 | 2015-05-27 | 霍夫曼-拉罗奇有限公司 | Chronic lymphocytic leukemia (Cll) biomarkers |
WO2012019024A2 (en) | 2010-08-04 | 2012-02-09 | Immunogen, Inc. | Her3-binding molecules and immunoconjugates thereof |
KR20130049196A (en) | 2010-08-05 | 2013-05-13 | 에프. 호프만-라 로슈 아게 | Anti-mhc antibody anti-viral cytokine fusion protein |
MX2013001336A (en) | 2010-08-13 | 2013-03-08 | Roche Glycart Ag | Anti-tenascin-c a2 antibodies and methods of use. |
US9011847B2 (en) | 2010-08-13 | 2015-04-21 | Roche Glycart, AG | Anti-FAP antibodies and methods of use |
WO2012024452A2 (en) | 2010-08-17 | 2012-02-23 | Ambrx, Inc. | Modified relaxin polypeptides and their uses |
US9567386B2 (en) | 2010-08-17 | 2017-02-14 | Ambrx, Inc. | Therapeutic uses of modified relaxin polypeptides |
ES2555864T3 (en) | 2010-08-19 | 2016-01-11 | F. Hoffmann-La Roche Ag | Assay for measuring antibody binding to a therapeutic monoclonal antibody |
GB201014033D0 (en) | 2010-08-20 | 2010-10-06 | Ucb Pharma Sa | Biological products |
KR20130103734A (en) | 2010-08-31 | 2013-09-24 | 제넨테크, 인크. | Biomarkers and methods of treatment |
WO2012032143A1 (en) | 2010-09-10 | 2012-03-15 | Novartis Forschungsstiftung, Zweigniederlassung, Friedrich Miescher Institute For Biomedical Research | Phosphorylated twist1 and metastasis |
US8551479B2 (en) | 2010-09-10 | 2013-10-08 | Oncomed Pharmaceuticals, Inc. | Methods for treating melanoma |
TWI480288B (en) | 2010-09-23 | 2015-04-11 | Lilly Co Eli | Formulations for bovine granulocyte colony stimulating factor and variants thereof |
KR20140008308A (en) | 2010-10-29 | 2014-01-21 | 이뮤노젠 아이엔씨 | Novel egfr-binding molecules and immunoconjugates thereof |
CN105399831A (en) | 2010-10-29 | 2016-03-16 | 伊缪诺金公司 | Non-antagonistic egfr-binding molecules and immunoconjugates thereof |
WO2012064836A1 (en) | 2010-11-10 | 2012-05-18 | Genentech, Inc. | Methods and compositions for neural disease immunotherapy |
US20140093506A1 (en) | 2010-11-15 | 2014-04-03 | Marc Buehler | Anti-fungal-agents |
EP2640831A1 (en) | 2010-11-17 | 2013-09-25 | Sea Lane Biotechnologies,llc. | Influenza virus neutralizing agents that mimic the binding site of an influenza neutralizing antibody |
WO2012071436A1 (en) | 2010-11-24 | 2012-05-31 | Genentech, Inc. | Method of treating autoimmune inflammatory disorders using il-23r loss-of-function mutants |
CN103619879A (en) | 2010-12-01 | 2014-03-05 | 奥尔德生物控股有限责任公司 | Anti-ngf compositions and use thereof |
US9067988B2 (en) | 2010-12-01 | 2015-06-30 | Alderbio Holdings Llc | Methods of preventing or treating pain using anti-NGF antibodies |
US9539324B2 (en) | 2010-12-01 | 2017-01-10 | Alderbio Holdings, Llc | Methods of preventing inflammation and treating pain using anti-NGF compositions |
US9884909B2 (en) | 2010-12-01 | 2018-02-06 | Alderbio Holdings Llc | Anti-NGF compositions and use thereof |
US11214610B2 (en) | 2010-12-01 | 2022-01-04 | H. Lundbeck A/S | High-purity production of multi-subunit proteins such as antibodies in transformed microbes such as Pichia pastoris |
US9078878B2 (en) | 2010-12-01 | 2015-07-14 | Alderbio Holdings Llc | Anti-NGF antibodies that selectively inhibit the association of NGF with TrkA, without affecting the association of NGF with p75 |
MX371228B (en) | 2010-12-16 | 2020-01-10 | Genentech Inc | Diagnosis and treatments relating to th2 inhibition. |
EP2655418B1 (en) | 2010-12-20 | 2017-10-04 | F. Hoffmann-La Roche AG | Anti-mesothelin antibodies and immunoconjugates |
WO2012087943A2 (en) | 2010-12-20 | 2012-06-28 | The Regents Of The University Of Michigan | Inhibitors of the epidermal growth factor receptor-heat shock protein 90 binding interaction |
CN103429261A (en) | 2010-12-22 | 2013-12-04 | 塞法隆澳大利亚股份有限公司 | Modified antibody with improved half-life |
BR112013015687A2 (en) | 2010-12-22 | 2016-10-11 | Genentech Inc | anti-pcsk9 antibody or an antibody fragment that binds to pcsk9, isolated nucleic acid, vector, host cell, method for making an anti-pcsk9 antibody, pharmaceutical composition, method of lowering ldl cholesterol level in a subject and method of treatment of hypercholesterolemia in a subject |
EP2661282A1 (en) | 2011-01-03 | 2013-11-13 | F.Hoffmann-La Roche Ag | A pharmaceutical composition of a complex of an anti-dig antibody and digoxigenin that is conjugated to a peptide |
GB201100282D0 (en) | 2011-01-07 | 2011-02-23 | Ucb Pharma Sa | Biological methods |
US10208349B2 (en) | 2011-01-07 | 2019-02-19 | Ucb Biopharma Sprl | Lipocalin 2 as a biomarker for IL-17 inhibitor therapy efficacy |
AU2012206431B2 (en) | 2011-01-14 | 2015-04-30 | UCB Biopharma SRL | Antibody molecules which bind IL-17A and IL-17F |
WO2012103165A2 (en) | 2011-01-26 | 2012-08-02 | Kolltan Pharmaceuticals, Inc. | Anti-kit antibodies and uses thereof |
WO2012106634A1 (en) | 2011-02-03 | 2012-08-09 | Alexion Pharmaceuticals, Inc. | Use of an anti-cd200 antibody for prolonging the survival of allografts |
WO2012129347A1 (en) | 2011-03-21 | 2012-09-27 | Biodesy, Llc | Classification of kinase inhibitors using nonlinear optical techniques |
SG10201602394QA (en) | 2011-03-29 | 2016-05-30 | Roche Glycart Ag | Antibody FC Variants |
MX342240B (en) | 2011-04-07 | 2016-09-21 | Genentech Inc | Anti-fgfr4 antibodies and methods of use. |
US10352936B2 (en) | 2011-04-14 | 2019-07-16 | Apoplogic Pharmaceuticals, Inc. | Use of tumor Fas expression to determine response to anti-cancer therapy |
EP2699264B1 (en) | 2011-04-20 | 2018-03-14 | Medlmmune, LLC | Antibodies and other molecules that bind b7-h1 and pd-1 |
JP6038121B2 (en) | 2011-04-21 | 2016-12-07 | ガーバン インスティテュート オブ メディカル リサーチ | Modified variable domain molecules and methods for their production and use B |
JP2014518624A (en) | 2011-05-12 | 2014-08-07 | ザ・ジョンズ・ホプキンス・ユニバーシティー | Assay reagent for neurogranin diagnostic kit |
US8679767B2 (en) | 2011-05-12 | 2014-03-25 | Genentech, Inc. | Multiple reaction monitoring LC-MS/MS method to detect therapeutic antibodies in animal samples using framework signature peptides |
EA030462B1 (en) | 2011-05-16 | 2018-08-31 | Дженентек, Инк. | Fgfr1 agonists and methods of use thereof |
NZ618016A (en) | 2011-05-21 | 2015-05-29 | Macrogenics Inc | Deimmunized serum-binding domains and their use for extending serum half-life |
DK2714738T3 (en) | 2011-05-24 | 2019-01-28 | Zyngenia Inc | MULTIVALENT AND MONOVALENT MULTISPECIFIC COMPLEXES AND THEIR APPLICATIONS |
WO2012168259A1 (en) | 2011-06-06 | 2012-12-13 | Novartis Forschungsstiftung, Zweigniederlassung | Protein tyrosine phosphatase, non-receptor type 11 (ptpn11) and triple-negative breast cancer |
WO2012170740A2 (en) | 2011-06-07 | 2012-12-13 | University Of Hawaii | Biomarker of asbestos exposure and mesothelioma |
WO2012170742A2 (en) | 2011-06-07 | 2012-12-13 | University Of Hawaii | Treatment and prevention of cancer with hmgb1 antagonists |
JP6058645B2 (en) | 2011-06-10 | 2017-01-11 | メディミューン,エルエルシー | Anti-Pseudomonas Psl binding molecules and uses thereof |
AU2012267786B2 (en) | 2011-06-10 | 2017-08-03 | Oregon Health & Science University | CMV glycoproteins and recombinant vectors |
MY166974A (en) | 2011-06-15 | 2018-07-27 | Hoffmann La Roche | Anti-human epo receptor antibodies and method of use |
MY160826A (en) | 2011-06-28 | 2017-03-31 | Berlin-Chemie Ag | Antibodies to bone marrow stromal antigen 1 |
PT2726094T (en) | 2011-06-28 | 2017-02-10 | Oxford Biotherapeutics Ltd | Therapeutic and diagnostic target |
CN103781493A (en) | 2011-06-30 | 2014-05-07 | 霍夫曼-拉罗奇有限公司 | Anti-c-met antibody formulations |
GB201112056D0 (en) | 2011-07-14 | 2011-08-31 | Univ Leuven Kath | Antibodies |
MX2014000578A (en) | 2011-07-14 | 2014-04-30 | Pfizer | Treatment with anti-pcsk9 antibodies. |
WO2013012733A1 (en) | 2011-07-15 | 2013-01-24 | Biogen Idec Ma Inc. | Heterodimeric fc regions, binding molecules comprising same, and methods relating thereto |
CN106167526A (en) | 2011-07-15 | 2016-11-30 | 昂考梅德药品有限公司 | RSPO bonding agent and its application |
US20130022551A1 (en) | 2011-07-22 | 2013-01-24 | Trustees Of Boston University | DEspR ANTAGONISTS AND AGONISTS AS THERAPEUTICS |
CN103842030B (en) | 2011-08-01 | 2018-07-31 | 霍夫曼-拉罗奇有限公司 | Use the method for PD-1 axis binding antagonists and mek inhibitor treating cancer |
CA2845536A1 (en) | 2011-08-15 | 2013-02-21 | Amplimmune, Inc. | Anti-b7-h4 antibodies and their uses |
CN103890007A (en) | 2011-08-17 | 2014-06-25 | 霍夫曼-拉罗奇有限公司 | Neuregulin antibodies and uses thereof |
EP2747781B1 (en) | 2011-08-23 | 2017-11-15 | Roche Glycart AG | Bispecific antibodies specific for t-cell activating antigens and a tumor antigen and methods of use |
RU2014109038A (en) | 2011-08-23 | 2015-09-27 | Рош Гликарт Аг | ANTIBODIES TO CHONDROITINSULFATE PROTEOGLYCAN MELANOMA |
RU2617970C2 (en) | 2011-08-23 | 2017-04-28 | Рош Гликарт Аг | ANTIBODIES WITHOUT Fc-FRAGMENT INCLUDING TWO FAB-FRAGMENT AND METHODS OF APPLICATION |
EP2753697A1 (en) | 2011-09-05 | 2014-07-16 | ETH Zürich | Biosynthetic gene cluster for the production of peptide/protein analogues |
ES2908046T3 (en) | 2011-09-09 | 2022-04-27 | Medimmune Ltd | Anti-siglec-15 antibodies and uses thereof. |
EP2568289A3 (en) | 2011-09-12 | 2013-04-03 | International AIDS Vaccine Initiative | Immunoselection of recombinant vesicular stomatitis virus expressing hiv-1 proteins by broadly neutralizing antibodies |
CN103930781A (en) | 2011-09-15 | 2014-07-16 | 霍夫曼-拉罗奇有限公司 | Methods of promoting differentiation |
KR20140064971A (en) | 2011-09-19 | 2014-05-28 | 제넨테크, 인크. | Combination treatments comprising c-met antagonists and b-raf antagonists |
PL3485903T3 (en) | 2011-09-23 | 2023-06-12 | Mereo Biopharma 5, Inc. | Vegf/dll4 binding agents and uses thereof |
CA2849011A1 (en) | 2011-10-05 | 2013-04-11 | Genentech, Inc. | Methods of treating liver conditions using notch2 antagonists |
CA2851261A1 (en) | 2011-10-06 | 2013-04-11 | The Board Of Trustees Of The University Of Illinois | Myosin binding protein-c for use in methods relating to diastolic heart failure |
WO2013054320A1 (en) | 2011-10-11 | 2013-04-18 | Tel Hashomer Medical Research Infrastructure And Services Ltd. | Antibodies to carcinoembryonic antigen-related cell adhesion molecule (ceacam) |
JP6190813B2 (en) | 2011-10-14 | 2017-08-30 | ジェネンテック, インコーポレイテッド | Zymogen activator |
EP2766028B1 (en) | 2011-10-14 | 2017-08-16 | F. Hoffmann-La Roche AG | Peptide inhibitors of bace1 |
MX2014004022A (en) | 2011-10-14 | 2014-04-30 | Genentech Inc | ANTI-HtrA1 ANTIBODIES AND METHODS OF USE. |
RU2014119426A (en) | 2011-10-15 | 2015-11-20 | Дженентек, Инк. | WAYS OF APPLICATION OF SCD1 ANTAGONISTS |
WO2013059531A1 (en) | 2011-10-20 | 2013-04-25 | Genentech, Inc. | Anti-gcgr antibodies and uses thereof |
EP2586461A1 (en) | 2011-10-27 | 2013-05-01 | Christopher L. Parks | Viral particles derived from an enveloped virus |
BR112014009953A2 (en) | 2011-10-28 | 2017-12-05 | Genentech Inc | tumor growth inhibition method, melanoma treatment, industrialized article and use |
AU2012332593B2 (en) | 2011-11-01 | 2016-11-17 | Bionomics, Inc. | Anti-GPR49 antibodies |
WO2013067057A1 (en) | 2011-11-01 | 2013-05-10 | Bionomics, Inc. | Anti-gpr49 antibodies |
EP2773373B1 (en) | 2011-11-01 | 2018-08-22 | Bionomics, Inc. | Methods of blocking cancer stem cell growth |
CN104053671A (en) | 2011-11-01 | 2014-09-17 | 生态学有限公司 | Antibodies and methods of treating cancer |
CA2853943C (en) | 2011-11-02 | 2015-12-08 | University Of Rochester | Anti-glucosaminidase passive immunization for staphylococcus aureus infections |
AU2012336028A1 (en) | 2011-11-07 | 2014-06-26 | Medimmune, Llc | Combination therapies using anti- Pseudomonas Psl and PcrV binding molecules |
US20140294732A1 (en) | 2011-11-08 | 2014-10-02 | Novartis Forschungsstiftung, Zweigniederlassung, Friedrich Miescher Institute | Early diagnostic of neurodegenerative diseases |
US20140314787A1 (en) | 2011-11-08 | 2014-10-23 | Novartis Forschungsstiftung, Zweigniederlassung, Friedrich Miescher Institute | Treatment for neurodegenerative diseases |
WO2013071233A1 (en) | 2011-11-10 | 2013-05-16 | The United States Of America, As Represented By The Secretary, Department Of Health & Human Services | Methods for detecting infectious agents and a novel virus detected thereby |
LT2776466T (en) | 2011-11-11 | 2017-11-27 | Ucb Biopharma Sprl | Albumin binding antibodies and binding fragments thereof |
JP5936702B2 (en) | 2011-11-11 | 2016-06-22 | ライナット ニューロサイエンス コーポレイション | Antibodies specific for TROP-2 and uses thereof |
KR20140105765A (en) | 2011-11-21 | 2014-09-02 | 이뮤노젠 아이엔씨 | Method of treatment of tumors that are resistant to egfr therapies by egfr antibody cytotoxic agent conjugate |
RU2014124842A (en) | 2011-11-21 | 2015-12-27 | Дженентек, Инк. | CLEANING ANTI-C-MET ANTIBODIES |
DK2797957T3 (en) | 2011-11-23 | 2019-09-23 | Medimmune Llc | BINDING MOLECULES SPECIFIC TO HER3 AND APPLICATIONS THEREOF |
EP2788024A1 (en) | 2011-12-06 | 2014-10-15 | F.Hoffmann-La Roche Ag | Antibody formulation |
SG11201403223PA (en) | 2011-12-22 | 2014-07-30 | Hoffmann La Roche | Expression vector organization, novel production cell generation methods and their use for the recombinant production of polypeptides |
CN107119073A (en) | 2011-12-22 | 2017-09-01 | 弗·哈夫曼-拉罗切有限公司 | The combination of expression vector element, new Cells for production production method and its purposes in restructuring produces polypeptide |
RU2625033C2 (en) | 2011-12-22 | 2017-07-11 | Ф. Хоффманн-Ля Рош Аг | Display system based on full length antibody for eukaryotic cells, and its application |
WO2013096791A1 (en) | 2011-12-23 | 2013-06-27 | Genentech, Inc. | Process for making high concentration protein formulations |
EP3539982A3 (en) | 2011-12-23 | 2020-01-15 | Pfizer Inc | Engineered antibody constant regions for site-specific conjugation and methods and uses therefor |
WO2013102825A1 (en) | 2012-01-02 | 2013-07-11 | Novartis Ag | Cdcp1 and breast cancer |
EP2802606B1 (en) | 2012-01-10 | 2018-04-25 | Biogen MA Inc. | Enhancement of transport of therapeutic molecules across the blood brain barrier |
CN104168920A (en) | 2012-01-18 | 2014-11-26 | 霍夫曼-拉罗奇有限公司 | Methods of using FGF19 modulators |
TW201335187A (en) | 2012-01-18 | 2013-09-01 | Genentech Inc | Anti-LRP5 antibodies and methods of use |
GB201201332D0 (en) | 2012-01-26 | 2012-03-14 | Imp Innovations Ltd | Method |
EP3575794A1 (en) | 2012-02-10 | 2019-12-04 | Seattle Genetics, Inc. | Detection and treatment of cd30+ cancers |
JP6545959B2 (en) | 2012-02-11 | 2019-07-17 | ジェネンテック, インコーポレイテッド | R-Spondin rearrangement and method of using the same |
SI2814842T1 (en) | 2012-02-15 | 2018-10-30 | Novo Nordisk A/S | Antibodies that bind peptidoglycan recognition protein 1 |
US9550830B2 (en) | 2012-02-15 | 2017-01-24 | Novo Nordisk A/S | Antibodies that bind and block triggering receptor expressed on myeloid cells-1 (TREM-1) |
EP2814587B1 (en) | 2012-02-15 | 2018-05-02 | F.Hoffmann-La Roche Ag | Fc-receptor based affinity chromatography |
JP6411218B2 (en) | 2012-02-15 | 2018-10-24 | ノヴォ ノルディスク アー/エス | Antibodies that bind to and block trigger receptor 1 (TREM-1) expressed in bone marrow cells |
GB201203051D0 (en) | 2012-02-22 | 2012-04-04 | Ucb Pharma Sa | Biological products |
GB201203071D0 (en) | 2012-02-22 | 2012-04-04 | Ucb Pharma Sa | Biological products |
PE20141909A1 (en) | 2012-03-13 | 2014-11-29 | Hoffmann La Roche | COMBINED THERAPY FOR THE TREATMENT OF OVARIAN CANCER |
RU2014141018A (en) | 2012-03-16 | 2016-05-10 | Ф. Хоффманн-Ля Рош Аг | METHODS OF TREATING MELANOMA WITH CANCER INHIBITORS |
KR20140142293A (en) | 2012-03-16 | 2014-12-11 | 제넨테크, 인크. | Engineered conformationally-stabilized proteins |
US9139863B2 (en) | 2012-03-16 | 2015-09-22 | Genentech, Inc. | Engineered conformationally-stabilized proteins |
DK2828282T3 (en) | 2012-03-20 | 2018-03-05 | Otago Innovation Ltd | Biomarkers |
WO2013139956A1 (en) | 2012-03-22 | 2013-09-26 | Thrombogenics Nv | Antibodies abrogating cell binding to lactadherin |
WO2013142808A1 (en) | 2012-03-23 | 2013-09-26 | The Government Of The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services | Pathogenic phlebovirus isolates and compositions and methods of use |
MX2014011500A (en) | 2012-03-27 | 2014-12-05 | Genentech Inc | Diagnosis and treatments relating to her3 inhibitors. |
US20150266961A1 (en) | 2012-03-29 | 2015-09-24 | Novartis Forschungsstiftung, Zweigniederlassung, Fridrich Miescher Institute | Inhibition of interleukin-8 and/or its receptor cxcr1 in the treatment of her2/her3-overexpressing breast cancer |
AR090549A1 (en) | 2012-03-30 | 2014-11-19 | Genentech Inc | ANTI-LGR5 AND IMMUNOCATE PLAYERS |
WO2013151649A1 (en) | 2012-04-04 | 2013-10-10 | Sialix Inc | Glycan-interacting compounds |
MX2014012843A (en) | 2012-04-24 | 2017-01-23 | Thrombogenics Nv | Anti-pdgf-c antibodies. |
EP2841951B1 (en) | 2012-04-25 | 2019-12-11 | Biodesy, Inc. | Methods for detecting allosteric modulators of proteins |
TW201402609A (en) | 2012-05-01 | 2014-01-16 | Genentech Inc | Anti-PMEL17 antibodies and immunoconjugates |
WO2013170191A1 (en) | 2012-05-11 | 2013-11-14 | Genentech, Inc. | Methods of using antagonists of nad biosynthesis from nicotinamide |
JP6122948B2 (en) | 2012-05-15 | 2017-04-26 | モルフォテック, インコーポレイテッド | Methods for the treatment of gastric cancer |
EP2852840B1 (en) | 2012-05-23 | 2019-10-09 | F.Hoffmann-La Roche Ag | Selection method for therapeutic agents |
KR102129636B1 (en) | 2012-05-31 | 2020-07-03 | 제넨테크, 인크. | Methods of treating cancer using pd-l1 axis binding antagonists and vegf antagonists |
CA2875980A1 (en) | 2012-06-06 | 2013-12-12 | Oncomed Pharmaceuticals, Inc. | Binding agents that modulate the hippo pathway and uses thereof |
JP2015530867A (en) | 2012-06-15 | 2015-10-29 | ジェネンテック, インコーポレイテッド | Anti-PCSK9 antibodies, formulations, dosing and methods of use |
ES2631608T3 (en) | 2012-06-27 | 2017-09-01 | International Aids Vaccine Initiative | Env-glycoprotein variant of HIV-1 |
EP2867674B1 (en) | 2012-06-28 | 2018-10-10 | UCB Biopharma SPRL | A method for identifying compounds of therapeutic interest |
WO2014001482A1 (en) | 2012-06-29 | 2014-01-03 | Novartis Forschungsstiftung, Zweigniererlassung, Friedrich Miescher Institute For Biomedical Research | Treating diseases by modulating a specific isoform of mkl1 |
PL2869837T3 (en) | 2012-07-04 | 2017-03-31 | F.Hoffmann-La Roche Ag | Anti-theophylline antibodies and methods of use |
KR20150030755A (en) | 2012-07-04 | 2015-03-20 | 에프. 호프만-라 로슈 아게 | Anti-biotin antibodies and methods of use |
PL2869848T3 (en) | 2012-07-04 | 2017-04-28 | F.Hoffmann-La Roche Ag | Covalently linked antigen-antibody conjugates |
CN110042114A (en) | 2012-07-05 | 2019-07-23 | 弗·哈夫曼-拉罗切有限公司 | Expression and excretory system |
WO2014006114A1 (en) | 2012-07-05 | 2014-01-09 | Novartis Forschungsstiftung, Zweigniederlassung Friedrich Miescher Institute For Biomedical Research | New treatment for neurodegenerative diseases |
US20150224190A1 (en) | 2012-07-06 | 2015-08-13 | Mohamed Bentires-Alj | Combination of a phosphoinositide 3-kinase inhibitor and an inhibitor of the IL-8/CXCR interaction |
CN104540524A (en) | 2012-07-09 | 2015-04-22 | 基因泰克公司 | Immunoconjugates comprising anti-CD22 antibodies |
AU2013288932A1 (en) | 2012-07-09 | 2014-12-11 | Genentech, Inc. | Immunoconjugates comprising anti - CD79b antibodies |
CA2874904A1 (en) | 2012-07-09 | 2014-01-16 | Genentech, Inc. | Immunoconjugates comprising anti-cd22 antibodies |
IN2014DN10652A (en) | 2012-07-09 | 2015-09-11 | Genentech Inc | |
MA37794B1 (en) | 2012-07-13 | 2017-07-31 | Roche Glycart Ag | Anti-vegf / anti-ang-2 bispecific antibodies and their use in the treatment of ocular vascular pathologies |
US9297806B2 (en) | 2012-08-01 | 2016-03-29 | The Johns Hopkins University | 5-hydroxymethylcytosine in human cancer |
GB201213652D0 (en) | 2012-08-01 | 2012-09-12 | Oxford Biotherapeutics Ltd | Therapeutic and diagnostic target |
WO2014025813A1 (en) | 2012-08-07 | 2014-02-13 | Genentech, Inc. | Combination therapy for the treatment of glioblastoma |
CN104755498B (en) | 2012-08-31 | 2019-06-18 | 伊缪诺金公司 | For detecting the diagnostic assay and kit of folacin receptor 1 |
AR092745A1 (en) | 2012-10-01 | 2015-04-29 | Univ Pennsylvania | COMPOSITIONS THAT INCLUDE AN ANTI-FAP UNION DOMAIN AND METHODS TO MAKE WHITE IN STROMAL CELLS FOR THE TREATMENT OF CANCER |
MX2015003616A (en) | 2012-10-08 | 2015-06-05 | Roche Glycart Ag | Fc-free antibodies comprising two fab-fragments and methods of use. |
BR112015008118A2 (en) | 2012-10-12 | 2017-12-05 | Brigham & Womens Hospital Inc | immune response booster |
JP2015536933A (en) | 2012-10-23 | 2015-12-24 | オンコメッド ファーマシューティカルズ インコーポレイテッド | Methods of treating neuroendocrine tumors using Wnt pathway binding agents |
WO2014071018A1 (en) | 2012-10-31 | 2014-05-08 | Oncomed Pharmaceuticals, Inc. | Methods and monitoring of treatment with a dll4 antagonist |
SG11201502989XA (en) | 2012-11-05 | 2015-05-28 | Genzyme Corp | Compositions and methods for treating proteinopathies |
US9725512B2 (en) | 2012-11-08 | 2017-08-08 | Hoffmann-La Roche Inc. | HER3 antibodies binding to the beta-hairpin of HER3 |
CN104968367B (en) | 2012-11-13 | 2018-04-13 | 弗·哈夫曼-拉罗切有限公司 | Antihemagglutinin antibody and application method |
WO2014085821A2 (en) | 2012-11-30 | 2014-06-05 | The Regents Of The University Of California | Fully human antibodies and fragments recognizing human c-met |
RU2691428C2 (en) | 2012-12-21 | 2019-06-13 | МЕДИММЬЮН, ЭлЭлСи | Antibodies to h7cr |
AU2013364065B2 (en) | 2012-12-21 | 2018-10-04 | Altrubio Inc. | Hydrophilic self-immolative linkers and conjugates thereof |
GB201223276D0 (en) | 2012-12-21 | 2013-02-06 | Ucb Pharma Sa | Antibodies and methods of producing same |
AU2013202668B2 (en) | 2012-12-24 | 2014-12-18 | Adelaide Research & Innovation Pty Ltd | Inhibition of cancer growth and metastasis |
WO2014107739A1 (en) | 2013-01-07 | 2014-07-10 | Eleven Biotherapeutics, Inc. | Antibodies against pcsk9 |
WO2014116749A1 (en) | 2013-01-23 | 2014-07-31 | Genentech, Inc. | Anti-hcv antibodies and methods of using thereof |
CN105073195A (en) | 2013-02-04 | 2015-11-18 | 昂科梅德制药有限公司 | Methods and monitoring of treatment with a Wnt pathway inhibitor |
GB201302447D0 (en) | 2013-02-12 | 2013-03-27 | Oxford Biotherapeutics Ltd | Therapeutic and diagnostic target |
WO2014129895A1 (en) | 2013-02-19 | 2014-08-28 | Stichting Vu-Vumc | Means and method for increasing the sensitivity of cancers for radiotherapy |
JP2016509045A (en) | 2013-02-22 | 2016-03-24 | エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト | How to treat cancer and prevent drug resistance |
CN105247072B (en) | 2013-02-25 | 2019-10-15 | 基因泰克公司 | The method and composition of detection and treatment drug resistance AKT mutant |
RU2015140921A (en) | 2013-02-26 | 2017-04-03 | Роше Гликарт Аг | ANTIBODIES TO MCSP |
CA2902263A1 (en) | 2013-03-06 | 2014-09-12 | Genentech, Inc. | Methods of treating and preventing cancer drug resistance |
EP2968565A2 (en) | 2013-03-14 | 2016-01-20 | Genentech, Inc. | Methods of treating cancer and preventing cancer drug resistance |
US9562099B2 (en) | 2013-03-14 | 2017-02-07 | Genentech, Inc. | Anti-B7-H4 antibodies and immunoconjugates |
KR20150127199A (en) | 2013-03-14 | 2015-11-16 | 제넨테크, 인크. | Anti-b7-h4 antibodies and immunoconjugates |
CA2903480A1 (en) | 2013-03-14 | 2014-09-25 | Genentech, Inc. | Combinations of a mek inhibitor compound with an her3/egfr inhibitor compound and methods of use |
US9168300B2 (en) | 2013-03-14 | 2015-10-27 | Oncomed Pharmaceuticals, Inc. | MET-binding agents and uses thereof |
JP6456356B2 (en) | 2013-03-15 | 2019-01-23 | ジェネンテック, インコーポレイテッド | IL-22 polypeptides and IL-22 Fc fusion proteins and methods of use |
RU2661111C2 (en) | 2013-03-15 | 2018-07-11 | Ац Иммуне С.А. | Anti-tau antibodies and methods of use |
EP2970471A2 (en) | 2013-03-15 | 2016-01-20 | F. Hoffmann-La Roche AG | Anti-crth2 antibodies and their use |
EP2972373B1 (en) | 2013-03-15 | 2019-10-09 | F.Hoffmann-La Roche Ag | Biomarkers and methods of treating pd-1 and pd-l1 related conditions |
SG11201507432XA (en) | 2013-03-15 | 2015-10-29 | Abbvie Inc | Antibody drug conjugate (adc) purification |
EA201890895A1 (en) | 2013-03-15 | 2019-02-28 | Зинджения, Инк. | MULTIVALENT AND MONOVALENT MULTIS-SPECIFIC COMPLEXES AND THEIR APPLICATION |
CN105339001A (en) | 2013-03-15 | 2016-02-17 | 基因泰克公司 | Methods of treating cancer and preventing cancer drug resistance |
JP6382935B2 (en) | 2013-03-15 | 2018-08-29 | アッヴィ・ドイチュラント・ゲー・エム・ベー・ハー・ウント・コー・カー・ゲー | Anti-EGFR antibody drug complex preparation |
AR095527A1 (en) | 2013-03-15 | 2015-10-21 | Biogen Idec Inc | FC-FACTOR IX POLYPEPTIDE FORMULATIONS IX |
WO2014151866A1 (en) | 2013-03-15 | 2014-09-25 | Genentech, Inc. | Compositions and methods for diagnosis and treatment of hepatic cancers |
SG11201508910WA (en) | 2013-04-29 | 2015-11-27 | Hoffmann La Roche | Fcrn-binding abolished anti-igf-1r antibodies and their use in the treatment of vascular eye diseases |
EA201501063A1 (en) | 2013-04-29 | 2016-05-31 | Ф. Хоффманн-Ля Рош Аг | CONNECTING HUMAN FcRn MODIFIED ANTIBODIES AND METHODS OF THEIR APPLICATION |
JP6618893B2 (en) | 2013-04-29 | 2019-12-11 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | Asymmetric antibodies with altered FC receptor binding and methods of use |
US10501802B2 (en) | 2013-04-30 | 2019-12-10 | Universite De Montreal | Biomarkers for acute myeloid leukemia |
SG10201913751RA (en) | 2013-05-06 | 2020-03-30 | Scholar Rock Inc | Compositions and methods for growth factor modulation |
KR102293064B1 (en) | 2013-05-20 | 2021-08-23 | 제넨테크, 인크. | Anti-transferrin receptor antibodies and methods of use |
BR112015029395A2 (en) | 2013-05-24 | 2017-09-19 | Medimmune Llc | ANTI-B7-H5 ANTIBODIES AND THEIR USES |
ES2891755T3 (en) | 2013-06-06 | 2022-01-31 | Pf Medicament | Anti-C10orf54 antibodies and uses thereof |
CN105636984A (en) | 2013-06-13 | 2016-06-01 | 法斯特弗沃德制药有限公司 | CD40 signalling inhibitor and a further compound, wherein the further compound is a bile acid, a bile acid derivative, an TGR5-receptor agonist, an FXR agonist or a combination thereof, for the treatment of chronic inflammation, and the prevention of gastrointestinal cancer or fibrosis. |
BR112016000853A2 (en) | 2013-07-16 | 2017-12-12 | Genentech Inc | methods for treating or delaying, reducing or inhibiting cancer relapse or progression and the progression of an immune-related disease in an individual, to increase, improve or stimulate an immune response or function in an individual and kit. |
KR101809072B1 (en) | 2013-08-02 | 2017-12-14 | 화이자 인코포레이티드 | Anti-cxcr4 antibodies and antibody-drug conjugates |
ES2761587T3 (en) | 2013-08-07 | 2020-05-20 | Friedrich Miescher Institute For Biomedical Res | New screening method for the treatment of Friedreich's ataxia |
KR102553717B1 (en) | 2013-08-26 | 2023-07-11 | 바이오엔테크 리서치 앤드 디벨롭먼트 인코포레이티드 | Nucleic acids encoding human antibodies to sialyl-lewis a |
AU2014312086B2 (en) | 2013-08-30 | 2020-03-12 | Immunogen, Inc. | Antibodies and assays for detection of folate receptor 1 |
US10617755B2 (en) | 2013-08-30 | 2020-04-14 | Genentech, Inc. | Combination therapy for the treatment of glioblastoma |
US10456470B2 (en) | 2013-08-30 | 2019-10-29 | Genentech, Inc. | Diagnostic methods and compositions for treatment of glioblastoma |
US20150065381A1 (en) | 2013-09-05 | 2015-03-05 | International Aids Vaccine Initiative | Methods of identifying novel hiv-1 immunogens |
WO2015042108A1 (en) | 2013-09-17 | 2015-03-26 | Genentech, Inc. | Methods of using anti-lgr5 antibodies |
US10414818B2 (en) | 2013-09-27 | 2019-09-17 | Roche Diagnostics Operations, Inc. | Thermus thermophilus SlyD FKBP domain specific antibodies |
US10058604B2 (en) | 2013-10-07 | 2018-08-28 | International Aids Vaccine Initiative | Soluble HIV-1 envelope glycoprotein trimers |
US20150132323A1 (en) | 2013-10-08 | 2015-05-14 | Immunogen, Inc. | Anti-FOLR1 Immunoconjugate Dosing Regimens |
KR20160068855A (en) | 2013-10-11 | 2016-06-15 | 제넨테크, 인크. | Nsp4 inhibitors and methods of use |
BR112016008477A2 (en) | 2013-10-18 | 2017-10-03 | Genentech Inc | BODIES, NUCLEIC ACID, HOST CELL, METHOD OF PRODUCING AN ANTIBODY, IMMUNOCONJUGATE, PHARMACEUTICAL FORMULATION AND USES OF THE ANTIBODY |
CN105849280B (en) | 2013-10-23 | 2020-11-06 | 豪夫迈·罗氏有限公司 | Methods of diagnosing and treating eosinophilic disorders |
WO2015066027A2 (en) | 2013-10-28 | 2015-05-07 | Dots Devices, Inc. | Allergen detection |
LT3071597T (en) | 2013-11-21 | 2020-10-12 | F. Hoffmann-La Roche Ag | Anti-alpha-synuclein antibodies and methods of use |
EP3074035B1 (en) | 2013-11-25 | 2020-05-13 | FameWave Ltd. | Compositions comprising anti-ceacam1 and anti-pd antibodies for cancer therapy |
WO2015085311A1 (en) | 2013-12-07 | 2015-06-11 | Case Western Reserve University | Compositions and methods of treating thrombosis |
BR112016013514B1 (en) | 2013-12-13 | 2022-04-19 | Stora Enso Oyj (Fi) | MULTI-LAYER CARDBOARD |
EP3080611B1 (en) | 2013-12-13 | 2018-11-14 | The General Hospital Corporation | Soluble high molecular weight (hmw) tau species and applications thereof |
WO2015089344A1 (en) | 2013-12-13 | 2015-06-18 | Genentech, Inc. | Anti-cd33 antibodies and immunoconjugates |
US20150190506A1 (en) | 2013-12-17 | 2015-07-09 | Genentech, Inc. | Combination therapy comprising ox40 binding agonists and pd-1 axis binding antagonists |
US9067998B1 (en) | 2014-07-15 | 2015-06-30 | Kymab Limited | Targeting PD-1 variants for treatment of cancer |
HUE050159T2 (en) | 2013-12-17 | 2020-11-30 | Genentech Inc | Anti-cd3 antibodies and methods of use |
MX2016007885A (en) | 2013-12-17 | 2017-01-11 | Genentech Inc | Methods of treating cancer using pd-1 axis binding antagonists and an anti-cd20 antibody. |
US9914769B2 (en) | 2014-07-15 | 2018-03-13 | Kymab Limited | Precision medicine for cholesterol treatment |
US9045545B1 (en) | 2014-07-15 | 2015-06-02 | Kymab Limited | Precision medicine by targeting PD-L1 variants for treatment of cancer |
US8992927B1 (en) | 2014-07-15 | 2015-03-31 | Kymab Limited | Targeting human NAV1.7 variants for treatment of pain |
US8986694B1 (en) | 2014-07-15 | 2015-03-24 | Kymab Limited | Targeting human nav1.7 variants for treatment of pain |
AU2014364601A1 (en) | 2013-12-17 | 2016-07-07 | Genentech, Inc. | Methods of treating HER2-positive cancers using PD-1 axis binding antagonists and anti-HER2 antibodies |
TWI670283B (en) | 2013-12-23 | 2019-09-01 | 美商建南德克公司 | Antibodies and methods of use |
KR102344991B1 (en) | 2013-12-24 | 2021-12-28 | 잔센파마슈티카엔.브이. | Anti-vista antibodies and fragments |
WO2015103549A1 (en) | 2014-01-03 | 2015-07-09 | The United States Of America, As Represented By The Secretary Department Of Health And Human Services | Neutralizing antibodies to hiv-1 env and their use |
RU2694981C2 (en) | 2014-01-03 | 2019-07-18 | Ф. Хоффманн-Ля Рош Аг | Covalently linked conjugates chelicar-antibody against chelicar and use thereof |
CA2933384A1 (en) | 2014-01-03 | 2015-07-09 | F. Hoffmann-La Roche Ag | Bispecific anti-hapten/anti-blood brain barrier receptor antibodies, complexes thereof and their use as blood brain barrier shuttles |
BR112016014945A2 (en) | 2014-01-03 | 2018-01-23 | F. Hoffmann-La Roche Ag | conjugate, pharmaceutical formulation and use |
KR102381685B1 (en) | 2014-01-06 | 2022-04-01 | 에프. 호프만-라 로슈 아게 | Monovalent blood brain barrier shuttle modules |
MX2016008539A (en) | 2014-01-15 | 2016-09-26 | Hoffmann La Roche | Fc-region variants with modified fcrn- and maintained protein a-binding properties. |
MX2016009515A (en) | 2014-01-24 | 2016-10-26 | Genentech Inc | Methods of using anti-steap1 antibodies and immunoconjugates. |
WO2015116902A1 (en) | 2014-01-31 | 2015-08-06 | Genentech, Inc. | G-protein coupled receptors in hedgehog signaling |
US11648335B2 (en) | 2014-01-31 | 2023-05-16 | Wake Forest University Health Sciences | Organ/tissue decellularization, framework maintenance and recellularization |
WO2015120187A1 (en) | 2014-02-05 | 2015-08-13 | The University Of Chicago | Chimeric antigen receptors recognizing cancer-spevific tn glycopeptide variants |
JP6685912B2 (en) | 2014-02-08 | 2020-04-22 | ジェネンテック, インコーポレイテッド | Alzheimer's disease treatment method |
SG10201901076WA (en) | 2014-02-08 | 2019-03-28 | Genentech Inc | Methods of treating alzheimer's disease |
KR102030891B1 (en) | 2014-02-12 | 2019-10-11 | 제넨테크, 인크. | Anti-jagged1 antibodies and methods of use |
KR20160124165A (en) | 2014-02-21 | 2016-10-26 | 제넨테크, 인크. | Anti-il-13/il-17 bispecific antibodies and uses thereof |
GB201403775D0 (en) | 2014-03-04 | 2014-04-16 | Kymab Ltd | Antibodies, uses & methods |
AU2015229035B2 (en) | 2014-03-14 | 2021-08-05 | Genentech, Inc. | Methods and compositions for secretion of heterologous polypeptides |
US9738702B2 (en) | 2014-03-14 | 2017-08-22 | Janssen Biotech, Inc. | Antibodies with improved half-life in ferrets |
US20170107294A1 (en) | 2014-03-21 | 2017-04-20 | Nordlandssykehuset Hf | Anti-cd14 antibodies and uses thereof |
EP4324481A2 (en) | 2014-03-21 | 2024-02-21 | Teva Pharmaceuticals International GmbH | Antagonist antibodies directed against calcitonin gene-related peptide and methods using same |
US10556945B2 (en) | 2014-03-21 | 2020-02-11 | Teva Pharmaceuticals International Gmbh | Antagonist antibodies directed against calcitonin gene-related peptide and methods using same |
JP2017516458A (en) | 2014-03-24 | 2017-06-22 | ジェネンテック, インコーポレイテッド | Cancer treatment with c-met antagonist and correlation with HGF expression of c-met antagonist |
AU2015241037B2 (en) | 2014-03-31 | 2020-10-15 | Genentech, Inc. | Anti-OX40 antibodies and methods of use |
RU2016142476A (en) | 2014-03-31 | 2018-05-07 | Дженентек, Инк. | COMBINED THERAPY, INCLUDING ANTI-ANGIOGENESIS AGENTS AND AGONISTS BINDING OX40 |
SG10202107077QA (en) | 2014-04-02 | 2021-07-29 | Hoffmann La Roche | Method for detecting multispecific antibody light chain mispairing |
US9546214B2 (en) | 2014-04-04 | 2017-01-17 | Bionomics, Inc. | Humanized antibodies that bind LGR5 |
MA50678A (en) | 2014-04-08 | 2020-08-05 | Boston Pharmaceuticals Inc | IL-21 SPECIFIC BINDING MOLECULES AND THEIR USES |
US10160812B2 (en) | 2014-04-11 | 2018-12-25 | Medimmune, Llc | Bispecific HER2 antibodies |
MX2016013635A (en) | 2014-04-18 | 2017-02-02 | Acceleron Pharma Inc | Methods for increasing red blood cell levels and treating sickle-cell disease. |
WO2015164615A1 (en) | 2014-04-24 | 2015-10-29 | University Of Oslo | Anti-gluten antibodies and uses thereof |
MX366359B (en) | 2014-04-27 | 2019-07-05 | Ccam Biotherapeutics Ltd | Humanized antibodies against ceacam1. |
US11427647B2 (en) | 2014-04-27 | 2022-08-30 | Famewave Ltd. | Polynucleotides encoding humanized antibodies against CEACAM1 |
US9753036B2 (en) | 2014-04-29 | 2017-09-05 | Edp Biotech Corporation | Methods and compositions for screening and detecting biomarkers |
SG11201608953WA (en) | 2014-04-30 | 2016-11-29 | Pfizer | Anti-ptk7 antibody-drug conjugates |
MA51519A (en) | 2014-05-05 | 2020-11-11 | Regeneron Pharma | HUMANIZED C5 AND C3 ANIMALS |
WO2015175874A2 (en) | 2014-05-16 | 2015-11-19 | Medimmune, Llc | Molecules with altered neonate fc receptor binding having enhanced therapeutic and diagnostic properties |
EP3145952A2 (en) | 2014-05-22 | 2017-03-29 | Genentech, Inc. | Anti-gpc3 antibodies and immunoconjugates |
RU2016144405A (en) | 2014-05-23 | 2018-06-26 | Дженентек, Инк. | MiT BIOMARKERS AND WAYS OF THEIR APPLICATION |
SG10201912986PA (en) | 2014-05-28 | 2020-02-27 | Agenus Inc | Anti-gitr antibodies and methods of use thereof |
GB201409558D0 (en) | 2014-05-29 | 2014-07-16 | Ucb Biopharma Sprl | Method |
WO2015187811A2 (en) | 2014-06-04 | 2015-12-10 | MabVax Therapeutics, Inc. | Human monoclonal antibodies to ganglioside gd2 |
CA2949982A1 (en) | 2014-06-11 | 2015-12-17 | Genentech, Inc. | Anti-lgr5 antibodies and uses thereof |
WO2015189816A1 (en) | 2014-06-13 | 2015-12-17 | Friedrich Miescher Institute For Biomedical Research | New treatment against influenza virus |
WO2015191986A1 (en) | 2014-06-13 | 2015-12-17 | Genentech, Inc. | Methods of treating and preventing cancer drug resistance |
WO2015192111A1 (en) | 2014-06-13 | 2015-12-17 | Acceleron Pharma, Inc. | Methods and compositions for treating ulcers |
CN106661124A (en) | 2014-06-20 | 2017-05-10 | 荷商台医(有限合伙)公司 | Anti-folate receptor aplha (FRA) antibody-drug conjugates and methods of using thereof |
EP3157535A1 (en) | 2014-06-23 | 2017-04-26 | Friedrich Miescher Institute for Biomedical Research | Methods for triggering de novo formation of heterochromatin and or epigenetic silencing with small rnas |
GB201411320D0 (en) | 2014-06-25 | 2014-08-06 | Ucb Biopharma Sprl | Antibody construct |
TW201623329A (en) | 2014-06-30 | 2016-07-01 | 亞佛瑞司股份有限公司 | Vaccines and monoclonal antibodies targeting truncated variants of osteopontin and uses thereof |
WO2016001830A1 (en) | 2014-07-01 | 2016-01-07 | Friedrich Miescher Institute For Biomedical Research | Combination of a brafv600e inhibitor and mertk inhibitor to treat melanoma |
CA2954687A1 (en) | 2014-07-10 | 2016-01-14 | Affiris Ag | Substances and methods for the use in prevention and/or treatment in huntington's disease |
BR112017000130A2 (en) | 2014-07-11 | 2018-01-09 | Genentech Inc | method for mitigating toxicity associated with notch pathway inhibition and cancer treatment method |
CN106460067A (en) | 2014-07-14 | 2017-02-22 | 豪夫迈·罗氏有限公司 | Diagnostic methods and compositions for treatment of glioblastoma |
EP3169361B1 (en) | 2014-07-15 | 2019-06-19 | F.Hoffmann-La Roche Ag | Compositions for treating cancer using pd-1 axis binding antagonists and mek inhibitors |
US9139648B1 (en) | 2014-07-15 | 2015-09-22 | Kymab Limited | Precision medicine by targeting human NAV1.9 variants for treatment of pain |
GB201412658D0 (en) | 2014-07-16 | 2014-08-27 | Ucb Biopharma Sprl | Molecules |
GB201412659D0 (en) | 2014-07-16 | 2014-08-27 | Ucb Biopharma Sprl | Molecules |
PE20170192A1 (en) | 2014-07-17 | 2017-03-16 | Novo Nordisk As | MUTAGENESIS TARGETED TO THE TRIGGERING RECEPTOR ANTIBODY SITE EXPRESSED IN TYPE 1 MELOID (TREM-1) TO REDUCE VISCOSITY |
CA2956991A1 (en) | 2014-08-06 | 2016-02-11 | Rinat Neuroscience Corp. | Methods for reducing ldl-cholesterol |
WO2016020799A1 (en) | 2014-08-06 | 2016-02-11 | Rinat Neuroscience Corp. | Methods for reducing ldl-cholesterol |
US11219670B2 (en) | 2014-09-05 | 2022-01-11 | The Johns Hopkins University | Targeting CAPN9/CAPNS2 activity as a therapeutic strategy for the treatment of myofibroblast differentiation and associated pathologies |
SG10201804931QA (en) | 2014-09-12 | 2018-07-30 | Genentech Inc | Anti-cll-1 antibodies and immunoconjugates |
CN114106185A (en) | 2014-09-12 | 2022-03-01 | 基因泰克公司 | anti-HER 2 antibodies and immunoconjugates |
EP3191518B1 (en) | 2014-09-12 | 2020-01-15 | Genentech, Inc. | Anti-b7-h4 antibodies and immunoconjugates |
EP3197500A1 (en) | 2014-09-17 | 2017-08-02 | Genentech, Inc. | Immunoconjugates comprising anti-her2 antibodies and pyrrolobenzodiazepines |
WO2016044697A1 (en) | 2014-09-19 | 2016-03-24 | The Johns Hopkins University | Biomarkers of cognitive dysfunction |
AU2015320678B2 (en) | 2014-09-23 | 2021-07-22 | Genentech, Inc. | Method of using anti-CD79b immunoconjugates |
US10472424B2 (en) | 2014-09-23 | 2019-11-12 | Pfizer Inc. | Treatment with anti-PCSK9 antibodies |
US20170298360A1 (en) | 2014-09-24 | 2017-10-19 | Friedrich Miescher Institute For Biomedical Research | Lats and breast cancer |
RU2021125449A (en) | 2014-10-01 | 2021-09-16 | Медиммьюн Лимитед | ANTIBODIES TO TICAGRELOR AND METHODS OF APPLICATION |
WO2016061389A2 (en) | 2014-10-16 | 2016-04-21 | Genentech, Inc. | Anti-alpha-synuclein antibodies and methods of use |
WO2016061460A1 (en) | 2014-10-17 | 2016-04-21 | Carnegie Mellon University | Enhanced biomolecule detection assays based on tyramide signal amplification and gammapna probes |
EP3209697A4 (en) | 2014-10-23 | 2018-05-30 | La Trobe University | Fn14-binding proteins and uses thereof |
UY36370A (en) | 2014-10-24 | 2016-04-29 | Bristol Myers Squibb Company Una Corporación Del Estado De Delaware | MODIFIED FGF-21 POLIPEPTIDES AND ITS USES |
US10626176B2 (en) | 2014-10-31 | 2020-04-21 | Jounce Therapeutics, Inc. | Methods of treating conditions with antibodies that bind B7-H4 |
EP3212233B1 (en) | 2014-10-31 | 2020-06-24 | Oncomed Pharmaceuticals, Inc. | Combination therapy for treatment of disease |
SG11201703521UA (en) | 2014-11-03 | 2017-05-30 | Genentech Inc | Methods and biomarkers for predicting efficacy and evaluation of an ox40 agonist treatment |
EP3215850B1 (en) | 2014-11-03 | 2019-07-03 | F. Hoffmann-La Roche AG | Assays for detecting t cell immune subsets and methods of use thereof |
WO2016073791A1 (en) | 2014-11-05 | 2016-05-12 | Genentech, Inc. | Methods of producing two chain proteins in bacteria |
KR102544705B1 (en) | 2014-11-05 | 2023-06-15 | 제넨테크, 인크. | Methods of producing two chain proteins in bacteria |
EP3611188B1 (en) | 2014-11-06 | 2022-05-04 | F. Hoffmann-La Roche AG | Fc-region variants with modified fcrn-binding and methods of use |
MX2017005150A (en) | 2014-11-06 | 2017-08-08 | Hoffmann La Roche | Fc-region variants with modified fcrn- and protein a-binding properties. |
RU2017119428A (en) | 2014-11-06 | 2018-12-06 | Дженентек, Инк. | COMBINED THERAPY, INCLUDING THE USE OF OX40-CONNECTING AGONISTS AND TIGIT INHIBITORS |
WO2016073157A1 (en) | 2014-11-06 | 2016-05-12 | Genentech, Inc. | Anti-ang2 antibodies and methods of use thereof |
BR112017009728A2 (en) | 2014-11-10 | 2018-02-06 | Genentech, Inc. | isolated antibodies, isolated nucleic acid, vector, host cell, method for producing antibody, composition, uses of an antibody and methods of treating a disorder |
EP3552488A1 (en) | 2014-11-10 | 2019-10-16 | F. Hoffmann-La Roche AG | Animal model for nephropathy and agents for treating the same |
HUE054339T2 (en) | 2014-11-10 | 2021-08-30 | Medimmune Ltd | Binding molecules specific for cd73 and uses thereof |
GB2538120A (en) | 2014-11-11 | 2016-11-09 | Medimmune Ltd | Therapeutic combinations comprising anti-CD73 antibodies and uses thereof |
US20170306046A1 (en) | 2014-11-12 | 2017-10-26 | Siamab Therapeutics, Inc. | Glycan-interacting compounds and methods of use |
US9879087B2 (en) | 2014-11-12 | 2018-01-30 | Siamab Therapeutics, Inc. | Glycan-interacting compounds and methods of use |
US10160795B2 (en) | 2014-11-14 | 2018-12-25 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Neutralizing antibodies to Ebola virus glycoprotein and their use |
US10434177B2 (en) | 2014-11-17 | 2019-10-08 | Carnegie Mellon University | Activatable two-component photosensitizers |
CA2967368A1 (en) | 2014-11-17 | 2016-05-26 | Genentech, Inc. | Combination therapy comprising ox40 binding agonists and pd-1 axis binding antagonists |
WO2016081643A1 (en) | 2014-11-19 | 2016-05-26 | Genentech, Inc. | Anti-transferrin receptor antibodies and methods of use |
WO2016081640A1 (en) | 2014-11-19 | 2016-05-26 | Genentech, Inc. | Anti-transferrin receptor / anti-bace1 multispecific antibodies and methods of use |
EP3845565A3 (en) | 2014-11-19 | 2021-09-08 | Genentech, Inc. | Antibodies against bace1 and use thereof for neural disease immunotherapy |
LT3789402T (en) | 2014-11-20 | 2022-09-26 | F. Hoffmann-La Roche Ag | Combination therapy of t cell activating bispecific antigen binding molecules and pd-1 axis binding antagonists |
MA41119A (en) | 2014-12-03 | 2017-10-10 | Acceleron Pharma Inc | METHODS OF TREATMENT OF MYELODYSPLASIC SYNDROMES AND SIDEROBLASTIC ANEMIA |
CN107206088A (en) | 2014-12-05 | 2017-09-26 | 豪夫迈·罗氏有限公司 | It is used for the method and composition for the treatment of cancer using the axle antagonists of PD 1 and HPK1 antagonists |
CA2966362A1 (en) | 2014-12-05 | 2016-06-09 | Genentech, Inc. | Anti-cd79b antibodies and methods of use |
BR112017011234A2 (en) | 2014-12-10 | 2018-03-27 | Genentech Inc | antibodies to the blood-brain barrier receptor and methods of use |
ES2934940T3 (en) | 2014-12-11 | 2023-02-28 | Pf Medicament | Anti-C10orf54 antibodies and uses thereof |
EP3233921B1 (en) | 2014-12-19 | 2021-09-29 | Chugai Seiyaku Kabushiki Kaisha | Anti-c5 antibodies and methods of use |
CA2972048C (en) | 2014-12-22 | 2023-03-07 | The Rockefeller University | Anti-mertk agonistic antibodies and uses thereof |
WO2016106286A1 (en) | 2014-12-23 | 2016-06-30 | Biodesy, Inc. | Attachment of proteins to interfaces for use in nonlinear optical detection |
US20160200815A1 (en) | 2015-01-05 | 2016-07-14 | Jounce Therapeutics, Inc. | Antibodies that inhibit tim-3:lilrb2 interactions and uses thereof |
SG11201705583XA (en) | 2015-01-09 | 2017-08-30 | Adalta Pty Ltd | Cxcr4 binding molecules |
JP2018511557A (en) | 2015-01-22 | 2018-04-26 | 中外製薬株式会社 | Combination and use of two or more anti-C5 antibodies |
JP6912386B2 (en) | 2015-01-26 | 2021-08-04 | ザ ユニバーシティー オブ シカゴ | CAR T cells that recognize cancer-specific IL13Rα2 |
WO2016123142A1 (en) | 2015-01-26 | 2016-08-04 | The University Of Chicago | IL13RAα2 BINDING AGENTS AND USE THEREOF IN CANCER TREATMENT |
EP3253793A4 (en) | 2015-02-02 | 2018-11-14 | i2 Pharmaceuticals, Inc. | Anti-surrogate light chain antibodies |
AU2016215155A1 (en) | 2015-02-04 | 2017-08-17 | F. Hoffmann-La Roche Ag | Tau antisense oligomers and uses thereof |
WO2016127000A1 (en) | 2015-02-04 | 2016-08-11 | Bristol-Myers Squibb Company | Methods of selecting therapeutic molecules |
KR102605798B1 (en) | 2015-02-05 | 2023-11-23 | 추가이 세이야쿠 가부시키가이샤 | Antibodies comprising an ion concentration dependent antigen-binding domain, fc region variants, il-8-binding antibodies, and uses therof |
HUE061070T2 (en) | 2015-03-03 | 2023-05-28 | Kymab Ltd | Antibodies, uses & methods |
CN107430117A (en) | 2015-03-16 | 2017-12-01 | 豪夫迈·罗氏有限公司 | Detection and quantitative IL 13 method and the purposes in diagnosing and treating Th2 relevant diseases |
WO2016146833A1 (en) | 2015-03-19 | 2016-09-22 | F. Hoffmann-La Roche Ag | Biomarkers for nad(+)-diphthamide adp ribosyltransferase resistance |
US10174292B2 (en) | 2015-03-20 | 2019-01-08 | International Aids Vaccine Initiative | Soluble HIV-1 envelope glycoprotein trimers |
EP3271389B8 (en) | 2015-03-20 | 2020-04-22 | The United States of America, as represented by the Secretary, Department of Health and Human Services | Neutralizing antibodies to gp120 and their use |
SI3273992T1 (en) | 2015-03-23 | 2020-09-30 | Jounce Therapeutics, Inc. | Antibodies to icos |
US9931394B2 (en) | 2015-03-23 | 2018-04-03 | International Aids Vaccine Initiative | Soluble HIV-1 envelope glycoprotein trimers |
WO2016154629A1 (en) | 2015-03-26 | 2016-09-29 | Woman & Infants' Hospital Of Rhode Island | Therapy for malignant disease |
EP3273994B1 (en) | 2015-03-27 | 2021-12-01 | University of Southern California | Car t-cell therapy directed to lhr for the treatment of solid tumors |
RU2754041C2 (en) | 2015-04-03 | 2021-08-25 | Еурека Терапьютикс, Инк. | Structures aimed at afp/mhc peptide complexes and types of their use |
MA41919A (en) | 2015-04-06 | 2018-02-13 | Acceleron Pharma Inc | ALK4 HETEROMULTIMERS: ACTRIIB AND THEIR USES |
EP3828199A1 (en) | 2015-04-06 | 2021-06-02 | Acceleron Pharma Inc. | Alk7: actriib heteromultimers and uses thereof |
CA2982115A1 (en) | 2015-04-06 | 2016-10-13 | President And Fellows Of Harvard College | Compositions and methods for non-myeloablative conditioning |
IL254887B2 (en) | 2015-04-07 | 2023-11-01 | Alector Llc | Anti-sortilin antibodies and methods of use thereof |
CN107709364A (en) | 2015-04-07 | 2018-02-16 | 豪夫迈·罗氏有限公司 | Antigen binding complex and application method with agonist activity |
KR102528825B1 (en) | 2015-04-13 | 2023-05-08 | 화이자 인코포레이티드 | Chimeric antigen receptors targeting b-cell maturation antigen |
CN108136002B (en) | 2015-04-13 | 2022-05-31 | 辉瑞公司 | Therapeutic antibodies and their use |
ES2870991T3 (en) | 2015-04-17 | 2021-10-28 | Alpine Immune Sciences Inc | Immunomodulatory proteins with adjustable affinities |
GB201506870D0 (en) | 2015-04-22 | 2015-06-03 | Ucb Biopharma Sprl | Method |
GB201506869D0 (en) | 2015-04-22 | 2015-06-03 | Ucb Biopharma Sprl | Method |
PL3286315T3 (en) | 2015-04-24 | 2021-11-02 | F. Hoffmann-La Roche Ag | Methods of identifying bacteria comprising binding polypeptides |
US10814012B2 (en) | 2015-04-29 | 2020-10-27 | University Of South Australia | Compositions and methods for administering antibodies |
CN107709363A (en) | 2015-05-01 | 2018-02-16 | 基因泰克公司 | Shelter anti-cd 3 antibodies and application method |
WO2016179194A1 (en) | 2015-05-04 | 2016-11-10 | Jounce Therapeutics, Inc. | Lilra3 and method of using the same |
CN107847594B (en) | 2015-05-06 | 2022-04-15 | 詹森生物科技公司 | Prostate Specific Membrane Antigen (PSMA) bispecific binding agents and uses thereof |
US10259882B2 (en) | 2015-05-07 | 2019-04-16 | Agenus Inc. | Anti-OX40 antibodies |
EP3736287A1 (en) | 2015-05-11 | 2020-11-11 | The Johns Hopkins University | Autoimmune antibodies for use in inhibiting cancer cell growth |
EP3936524A3 (en) | 2015-05-11 | 2022-06-15 | F. Hoffmann-La Roche AG | Compositions and methods of treating lupus nephritis |
MX2017014381A (en) | 2015-05-12 | 2018-03-02 | Genentech Inc | Therapeutic and diagnostic methods for cancer. |
EP3718569B1 (en) | 2015-05-22 | 2023-05-03 | Translational Drug Development, LLC | Benzamide and active compound compositions and methods of use |
EA039951B1 (en) | 2015-05-27 | 2022-03-31 | Юсб Биофарма Спрл | Inhibitor of csf-1r activity for use in the treatment or prophylaxis of epilepsy or parkinson's disease and pharmaceutical composition thereof |
MX2017015046A (en) | 2015-05-29 | 2018-05-17 | Agenus Inc | Anti-ctla-4 antibodies and methods of use thereof. |
ES2789500T5 (en) | 2015-05-29 | 2023-09-20 | Hoffmann La Roche | Therapeutic and diagnostic procedures for cancer |
WO2016196343A1 (en) | 2015-05-29 | 2016-12-08 | Genentech, Inc. | Humanized anti-ebola virus glycoprotein antibodies and methods of use |
AR105618A1 (en) | 2015-05-29 | 2017-10-25 | Genentech Inc | METHODATION OF THE PROMOTER OF THE BINDING TO THE PROGRAMMED DEATH RECEIVER (PD-L1) IN CANCER |
JP2018516933A (en) | 2015-06-02 | 2018-06-28 | ジェネンテック, インコーポレイテッド | Compositions and methods for treating neurological disorders using anti-IL-34 antibodies |
WO2016196975A1 (en) | 2015-06-03 | 2016-12-08 | The United States Of America, As Represented By The Secretary Department Of Health & Human Services | Neutralizing antibodies to hiv-1 env and their use |
US10711064B2 (en) | 2015-06-04 | 2020-07-14 | University Of Southern California | Lym-1 and Lym-2 targeted CAR cell immunotherapy |
AU2016270858B2 (en) | 2015-06-05 | 2022-04-28 | Ac Immune Sa | Anti-Tau antibodies and methods of use |
JP2018518483A (en) | 2015-06-08 | 2018-07-12 | ジェネンテック, インコーポレイテッド | Methods of treating cancer using anti-OX40 antibodies and PD-1 axis binding antagonists |
JP2018521019A (en) | 2015-06-08 | 2018-08-02 | ジェネンテック, インコーポレイテッド | Method of treating cancer using anti-OX40 antibody |
JP2018518491A (en) | 2015-06-12 | 2018-07-12 | アレクトル エルエルシー | Anti-CD33 antibody and method of use thereof |
CN116063499A (en) | 2015-06-12 | 2023-05-05 | 艾利妥 | anti-CD 33 antibodies and methods of use thereof |
AR104987A1 (en) | 2015-06-15 | 2017-08-30 | Genentech Inc | ANTIBODY-DRUG IMMUNOCUJADOS UNITED BY NON-PEPTIDIC LINKERS |
WO2016205520A1 (en) | 2015-06-16 | 2016-12-22 | Genentech, Inc. | Humanized and affinity matured antibodies to fcrh5 and methods of use |
US10501545B2 (en) | 2015-06-16 | 2019-12-10 | Genentech, Inc. | Anti-CLL-1 antibodies and methods of use |
EP3310811B1 (en) | 2015-06-16 | 2021-06-16 | Genentech, Inc. | Anti-cd3 antibodies and methods of use |
CA2986263A1 (en) | 2015-06-17 | 2016-12-22 | Genentech, Inc. | Methods of treating locally advanced or metastatic breast cancers using pd-1 axis binding antagonists and taxanes |
AU2016280159A1 (en) | 2015-06-17 | 2017-12-07 | Genentech, Inc. | Anti-HER2 antibodies and methods of use |
GB201510758D0 (en) | 2015-06-18 | 2015-08-05 | Ucb Biopharma Sprl | Novel TNFa structure for use in therapy |
US20180188257A1 (en) | 2015-06-19 | 2018-07-05 | University Of Rochester | Septin proteins as novel biomarkers for detection and treatment of müllerian cancers |
CA2990360C (en) | 2015-06-24 | 2024-02-13 | Janssen Pharmaceutica Nv | Anti-vista antibodies and fragments |
MX2017016645A (en) | 2015-06-29 | 2018-11-09 | Genentech Inc | Type ii anti-cd20 antibody for use in organ transplantation. |
HUE053619T2 (en) | 2015-06-29 | 2021-07-28 | Immunogen Inc | Anti-cd123 antibodies and conjugates and derivatives thereof |
GB201601077D0 (en) | 2016-01-20 | 2016-03-02 | Ucb Biopharma Sprl | Antibody molecule |
GB201601075D0 (en) | 2016-01-20 | 2016-03-02 | Ucb Biopharma Sprl | Antibodies molecules |
GB201601073D0 (en) | 2016-01-20 | 2016-03-02 | Ucb Biopharma Sprl | Antibodies |
WO2017015334A1 (en) | 2015-07-21 | 2017-01-26 | Saint Louis University | Compositions and methods for diagnosing and treating endometriosis-related infertility |
EP4218792A1 (en) | 2015-08-04 | 2023-08-02 | Acceleron Pharma Inc. | Composition for treating myeloproliferative disorders |
CN105384825B (en) | 2015-08-11 | 2018-06-01 | 南京传奇生物科技有限公司 | A kind of bispecific chimeric antigen receptor and its application based on single domain antibody |
CN114605548A (en) | 2015-09-01 | 2022-06-10 | 艾吉纳斯公司 | anti-PD-1 antibodies and methods of use thereof |
EP3349796A4 (en) | 2015-09-17 | 2019-05-29 | ImmunoGen, Inc. | Therapeutic combinations comprising anti-folr1 immunoconjugates |
CN108271372B (en) | 2015-09-18 | 2021-07-09 | 中外制药株式会社 | IL-8-binding antibodies and uses thereof |
BR112018005737A2 (en) | 2015-09-23 | 2018-10-09 | Genentech Inc | antibodies, polynucleotide, vector, host cell, method for producing antibody, for reducing or inhibiting angiogenesis, for treating a disorder associated with angiogenesis, for inhibiting vascular permeability, composition, antibody conjugate, fusion protein, for identifying a change residues, antibody use, conjugate use and protein use |
EP3569244A1 (en) | 2015-09-23 | 2019-11-20 | CytoImmune Therapeutics, LLC | Flt3 directed car cells for immunotherapy |
AU2016326609B2 (en) | 2015-09-23 | 2023-03-09 | Mereo Biopharma 5, Inc. | Methods and compositions for treatment of cancer |
EP3352791B1 (en) | 2015-09-24 | 2019-10-30 | AbVitro LLC | Hiv antibody compositions and methods of use |
CA3000386A1 (en) | 2015-09-30 | 2017-04-06 | Merck Patent Gmbh | Combination of a pd-1 axis binding antagonist and an alk inhibitor for treating alk-negative cancer |
MA43345A (en) | 2015-10-02 | 2018-08-08 | Hoffmann La Roche | PYRROLOBENZODIAZEPINE ANTIBODY-DRUG CONJUGATES AND METHODS OF USE |
JP6654694B2 (en) | 2015-10-02 | 2020-02-26 | エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト | Anti-PD1 antibody and method of use |
US11161912B2 (en) | 2015-10-13 | 2021-11-02 | Technion Research & Development Foundation Limited | Heparanase-neutralizing monoclonal antibodies |
MA43354A (en) | 2015-10-16 | 2018-08-22 | Genentech Inc | CONJUGATE DRUG CONJUGATES WITH CLOUDY DISULPHIDE |
MA45326A (en) | 2015-10-20 | 2018-08-29 | Genentech Inc | CALICHEAMICIN-ANTIBODY-DRUG CONJUGATES AND METHODS OF USE |
CN108350505A (en) | 2015-10-22 | 2018-07-31 | 震动疗法股份有限公司 | Genetic marker for measuring ICOS expression |
SG11201802895QA (en) | 2015-10-23 | 2018-05-30 | Eureka Therapeutics Inc | Antibody/t-cell receptor chimeric constructs and uses thereof |
SG11201802887PA (en) | 2015-10-27 | 2018-05-30 | Ucb Biopharma Sprl | Methods of treatment using anti-il-17a/f antibodies |
US20180348224A1 (en) | 2015-10-28 | 2018-12-06 | Friedrich Miescher Institute For Biomedical Resear Ch | Tenascin-w and biliary tract cancers |
EP3184547A1 (en) | 2015-10-29 | 2017-06-28 | F. Hoffmann-La Roche AG | Anti-tpbg antibodies and methods of use |
WO2017075173A2 (en) | 2015-10-30 | 2017-05-04 | Genentech, Inc. | Anti-factor d antibodies and conjugates |
AU2016344399B2 (en) | 2015-10-30 | 2019-03-28 | Genentech, Inc. | Anti-HtrA1 antibodies and methods of use thereof |
US11273151B2 (en) | 2015-11-04 | 2022-03-15 | Icahn School Of Medicine At Mount Sinai | Methods of treating tumors and cancer, and identifying candidate subjects for such treatment |
EP3371217A1 (en) | 2015-11-08 | 2018-09-12 | H. Hoffnabb-La Roche Ag | Methods of screening for multispecific antibodies |
EP3374398B1 (en) | 2015-11-10 | 2020-03-18 | MedImmune, LLC | Binding molecules specific for asct2 and uses thereof |
IL302822A (en) | 2015-11-12 | 2023-07-01 | Seagen Inc | Glycan-interacting compounds and methods of use |
US10550170B2 (en) | 2015-11-23 | 2020-02-04 | Acceleron Pharma Inc. | Methods for treating vascular eye disorders with actrii antagonists |
MX2018006613A (en) | 2015-12-02 | 2019-01-30 | Stcube & Co Inc | Antibodies and molecules that immunospecifically bind to btn1a1 and the therapeutic uses thereof. |
KR20180100122A (en) | 2015-12-02 | 2018-09-07 | 주식회사 에스티사이언스 | Antibodies specific for glycated BTLA (B- and T-lymphocyte weakening factor) |
GB201521389D0 (en) | 2015-12-03 | 2016-01-20 | Ucb Biopharma Sprl | Method |
GB201521391D0 (en) | 2015-12-03 | 2016-01-20 | Ucb Biopharma Sprl | Antibodies |
GB201521383D0 (en) | 2015-12-03 | 2016-01-20 | Ucb Biopharma Sprl And Ucb Celltech | Method |
GB201521393D0 (en) | 2015-12-03 | 2016-01-20 | Ucb Biopharma Sprl | Antibodies |
GB201521382D0 (en) | 2015-12-03 | 2016-01-20 | Ucb Biopharma Sprl | Antibodies |
EP3178848A1 (en) | 2015-12-09 | 2017-06-14 | F. Hoffmann-La Roche AG | Type ii anti-cd20 antibody for reducing formation of anti-drug antibodies |
MX2018005229A (en) | 2015-12-09 | 2019-04-29 | F HoffmannLa Roche Ag | Type ii anti-cd20 antibody for reducing formation of anti-drug antibodies. |
WO2017097889A1 (en) | 2015-12-10 | 2017-06-15 | Katholieke Universiteit Leuven | Anti adamts13 antibodies and their use for treatment or prevention of haemorrhagic disorders due to ventricular assist device |
CN108401431B (en) | 2015-12-18 | 2022-01-25 | 中外制药株式会社 | anti-C5 antibodies and methods of use |
EP3405478A4 (en) | 2015-12-23 | 2019-10-30 | Moonshot Pharma LLC | Methods for inducing an immune response by inhibition of nonsense mediated decay |
WO2017118307A1 (en) | 2016-01-05 | 2017-07-13 | 江苏恒瑞医药股份有限公司 | Pcsk9 antibody, antigen-binding fragment thereof, and medical uses thereof |
SG11201805557SA (en) | 2016-01-08 | 2018-07-30 | Bioalliance Cv | Tetravalent anti-psgl-1 antibodies and uses thereof |
CN108368179B (en) | 2016-01-08 | 2022-08-23 | 豪夫迈·罗氏有限公司 | Methods of treating CEA positive cancers using PD-1 axis binding antagonists and anti-CEA/anti-CD 3 bispecific antibodies |
CA3011739A1 (en) | 2016-01-20 | 2017-07-27 | Genentech, Inc. | High dose treatments for alzheimer's disease |
SG11201805872SA (en) | 2016-01-21 | 2018-08-30 | Pfizer | Chimeric antigen receptors targeting epidermal growth factor receptor variant iii |
DK3405490T3 (en) | 2016-01-21 | 2022-01-10 | Pfizer | MONO- AND BISPECIFIC ANTIBODIES AGAINST EPIDERMAL GROWTH FACTOR RECEPTOR VARIANT III AND CD3 AND USES THEREOF |
GB201602413D0 (en) | 2016-02-10 | 2016-03-23 | Nascient Ltd | Method |
TWI756204B (en) | 2016-02-12 | 2022-03-01 | 比利時商楊森製藥公司 | Anti-vista antibodies and fragments, uses thereof, and methods of identifying same |
CA3015528A1 (en) | 2016-02-29 | 2017-09-08 | Genentech, Inc. | Therapeutic and diagnostic methods for cancer |
JP6987072B2 (en) | 2016-03-10 | 2021-12-22 | アクセレロン ファーマ インコーポレーテッド | Activin type 2 receptor binding protein and its use |
BR112018067951A2 (en) | 2016-03-10 | 2019-02-05 | Viela Bio Inc | ilt7-binding molecules and methods of using these |
AU2017235097B2 (en) | 2016-03-15 | 2023-08-31 | Chugai Seiyaku Kabushiki Kaisha | Methods of treating cancers using PD-1 axis binding antagonists and anti-GPC3 antibodies |
CA3018081A1 (en) | 2016-03-22 | 2017-09-28 | Bionomics Limited | Administration of an anti-lgr5 monoclonal antibody |
US20170315132A1 (en) | 2016-03-25 | 2017-11-02 | Genentech, Inc. | Multiplexed total antibody and antibody-conjugated drug quantification assay |
CA3019164A1 (en) | 2016-03-29 | 2017-10-05 | Janssen Biotech, Inc. | Method of treating psoriasis with increased interval dosing of anti-il12/23 antibody |
WO2017175058A1 (en) | 2016-04-07 | 2017-10-12 | Janssen Pharmaceutica Nv | Anti-vista antibodies and fragments, uses thereof, and methods of identifying same |
WO2017180864A1 (en) | 2016-04-14 | 2017-10-19 | Genentech, Inc. | Anti-rspo3 antibodies and methods of use |
PL3443350T3 (en) | 2016-04-15 | 2021-05-31 | F. Hoffmann-La Roche Ag | Methods for monitoring and treating cancer |
JP2019515670A (en) | 2016-04-15 | 2019-06-13 | ジェネンテック, インコーポレイテッド | Methods for monitoring and treating cancer |
EP3448881B1 (en) | 2016-04-26 | 2023-06-07 | Icahn School of Medicine at Mount Sinai | Treatment of hippo pathway mutant tumors and methods of identifying subjects as candidates for treatment |
PE20181890A1 (en) | 2016-05-02 | 2018-12-11 | Hoffmann La Roche | CONTORSBODY - A MONOCATENARIO DIANA LEAGUE |
WO2017194441A1 (en) | 2016-05-11 | 2017-11-16 | F. Hoffmann-La Roche Ag | Modified anti-tenascin antibodies and methods of use |
JP7084878B2 (en) | 2016-05-16 | 2022-06-15 | 武田薬品工業株式会社 | Anti-factor IX Padua antibody |
EP3458101B1 (en) | 2016-05-20 | 2020-12-30 | H. Hoffnabb-La Roche Ag | Protac antibody conjugates and methods of use |
WO2017205465A2 (en) | 2016-05-24 | 2017-11-30 | Griswold Karl Edwin | Antibodies and methods of making same |
CN109313200B (en) | 2016-05-27 | 2022-10-04 | 豪夫迈·罗氏有限公司 | Bioanalytical methods for characterizing site-specific antibody-drug conjugates |
CA3024508A1 (en) | 2016-05-27 | 2017-11-30 | Agenus Inc. | Anti-tim-3 antibodies and methods of use thereof |
TW201902512A (en) | 2016-06-02 | 2019-01-16 | 瑞士商赫孚孟拉羅股份公司 | treatment method |
EP3252078A1 (en) | 2016-06-02 | 2017-12-06 | F. Hoffmann-La Roche AG | Type ii anti-cd20 antibody and anti-cd20/cd3 bispecific antibody for treatment of cancer |
MY194619A (en) | 2016-06-02 | 2022-12-07 | Abbvie Inc | Glucocorticoid receptor agonist and immunoconjugates thereof |
US10639378B2 (en) | 2016-06-06 | 2020-05-05 | Genentech, Inc. | Silvestrol antibody-drug conjugates and methods of use |
EP3464345A1 (en) | 2016-06-06 | 2019-04-10 | F. Hoffmann-La Roche AG | Fusion proteins for ophthalmology with increased eye retention |
CN116143918A (en) | 2016-06-24 | 2023-05-23 | 豪夫迈·罗氏有限公司 | Anti-polyubiquitin multispecific antibodies |
JP6983824B2 (en) | 2016-07-04 | 2021-12-17 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | New antibody format |
EP3481835A4 (en) | 2016-07-05 | 2020-02-26 | Blade Therapeutics, Inc. | Calpain modulators and therapeutic uses thereof |
CN109689685A (en) | 2016-07-08 | 2019-04-26 | 斯塔滕生物技术有限公司 | Anti- APOC3 antibody and its application method |
AU2017296237A1 (en) | 2016-07-15 | 2019-01-03 | Poseida Therapeutics, Inc. | Chimeric antigen receptors (CARS) specific for MUC1 and methods for their use |
US10722558B2 (en) | 2016-07-15 | 2020-07-28 | Acceleron Pharma Inc. | Compositions and methods for treating pulmonary hypertension |
AU2017296236A1 (en) | 2016-07-15 | 2019-01-03 | Poseida Therapeutics, Inc. | Chimeric antigen receptors and methods for use |
WO2018014260A1 (en) | 2016-07-20 | 2018-01-25 | Nanjing Legend Biotech Co., Ltd. | Multispecific antigen binding proteins and methods of use thereof |
MA45811A (en) | 2016-07-27 | 2019-06-05 | Acceleron Pharma Inc | METHODS AND COMPOSITIONS OF TREATMENT OF DISEASE. |
KR102591955B1 (en) | 2016-07-29 | 2023-10-19 | 추가이 세이야쿠 가부시키가이샤 | Bispecific Antibody with Enhanced FVIII Carrier Function Replacement Activity |
WO2018027204A1 (en) | 2016-08-05 | 2018-02-08 | Genentech, Inc. | Multivalent and multiepitopic anitibodies having agonistic activity and methods of use |
CN109689090B (en) | 2016-08-05 | 2023-12-26 | 免疫医疗有限责任公司 | anti-O2 antibodies and uses thereof |
US11053308B2 (en) | 2016-08-05 | 2021-07-06 | Chugai Seiyaku Kabushiki Kaisha | Method for treating IL-8-related diseases |
JP7250674B2 (en) | 2016-08-08 | 2023-04-03 | エフ・ホフマン-ラ・ロシュ・アクチェンゲゼルシャフト | CANCER TREATMENT AND DIAGNOSTIC METHOD |
WO2018031662A1 (en) | 2016-08-11 | 2018-02-15 | Genentech, Inc. | Pyrrolobenzodiazepine prodrugs and antibody conjugates thereof |
SG10201607778XA (en) | 2016-09-16 | 2018-04-27 | Chugai Pharmaceutical Co Ltd | Anti-Dengue Virus Antibodies, Polypeptides Containing Variant Fc Regions, And Methods Of Use |
JP6976315B2 (en) | 2016-09-19 | 2021-12-08 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | Affinity chromatography based on complement factors |
WO2018055574A1 (en) | 2016-09-23 | 2018-03-29 | Teva Pharmaceuticals International Gmbh | Treating refractory migraine |
AU2017331592A1 (en) | 2016-09-23 | 2019-04-11 | Teva Pharmaceuticals International Gmbh | Treating cluster headache |
PT3528838T (en) | 2016-09-23 | 2023-09-04 | Hoffmann La Roche | Uses of il-13 antagonists for treating atopic dermatitis |
AU2017336523B2 (en) | 2016-09-28 | 2022-07-21 | Blade Therapeutics, Inc. | Calpain modulators and therapeutic uses thereof |
GB201616596D0 (en) | 2016-09-29 | 2016-11-16 | Nascient Limited | Epitope and antibodies |
MX2019003703A (en) | 2016-09-30 | 2020-08-13 | Janssen Biotech Inc | Safe and effective method of treating psoriasis with anti-il23 specific antibody. |
CN110198743B (en) | 2016-10-05 | 2023-07-18 | 艾科赛扬制药股份有限公司 | Compositions and methods for treating kidney disease |
EP3522933B1 (en) | 2016-10-05 | 2021-12-15 | F. Hoffmann-La Roche AG | Methods for preparing antibody drug conjugates |
EP3523451A1 (en) | 2016-10-06 | 2019-08-14 | Genentech, Inc. | Therapeutic and diagnostic methods for cancer |
WO2018068201A1 (en) | 2016-10-11 | 2018-04-19 | Nanjing Legend Biotech Co., Ltd. | Single-domain antibodies and variants thereof against ctla-4 |
AU2017343621B2 (en) | 2016-10-11 | 2021-12-02 | Agenus Inc. | Anti-LAG-3 antibodies and methods of use thereof |
WO2018075408A1 (en) | 2016-10-17 | 2018-04-26 | Alexion Pharmaceuticals, Inc. | Methods of treating acute myeloid leukemia (aml) with combinations of anti-cd200 antibodies, cytarabine, and daunorubicin |
JP7160484B2 (en) | 2016-10-19 | 2022-10-25 | メディミューン,エルエルシー | ANTI-O1 ANTIBODY AND USES THEREOF |
US11249082B2 (en) | 2016-10-29 | 2022-02-15 | University Of Miami | Zika virus assay systems |
CN110267678A (en) | 2016-10-29 | 2019-09-20 | 霍夫曼-拉罗奇有限公司 | Anti- MIC antibody and application method |
SG11201903842YA (en) | 2016-11-02 | 2019-05-30 | Immunogen Inc | Combination treatment with antibody-drug conjugates and parp inhibitors |
RS62589B1 (en) | 2016-11-02 | 2021-12-31 | Jounce Therapeutics Inc | Antibodies to pd-1 and uses thereof |
WO2018083248A1 (en) | 2016-11-03 | 2018-05-11 | Kymab Limited | Antibodies, combinations comprising antibodies, biomarkers, uses & methods |
CA3042989A1 (en) | 2016-11-07 | 2018-05-11 | Junho Chung | Anti-family with sequence similarity 19, member a5 antibodies and method of use thereof |
AU2017362222A1 (en) | 2016-11-16 | 2019-05-30 | Janssen Biotech, Inc. | Method of treating psoriasis with anti-IL-23 specific antibody |
WO2018094143A1 (en) | 2016-11-17 | 2018-05-24 | Siamab Therapeutics, Inc. | Glycan-interacting compounds and methods of use |
TW201829463A (en) | 2016-11-18 | 2018-08-16 | 瑞士商赫孚孟拉羅股份公司 | Anti-hla-g antibodies and use thereof |
JP7080234B2 (en) | 2016-11-23 | 2022-06-03 | トランスレイショナル・ドラッグ・ディベロップメント・エルエルシー | Benzamide and active compound compositions and methods of use |
KR20190080949A (en) | 2016-11-23 | 2019-07-08 | 바이오버라티브 테라퓨틱스 인크. | A bispecific antibody that binds to coagulation factor IX and coagulation factor X |
WO2018102594A1 (en) | 2016-12-01 | 2018-06-07 | Alexion Pharmaceuticals, Inc. | Methods of treating solid tumors with anti-cd200 antibodies |
SG10201911351SA (en) | 2016-12-07 | 2020-02-27 | Genentech Inc | Anti-tau antibodies and methods of use |
EP3551660B1 (en) | 2016-12-07 | 2023-09-13 | Agenus Inc. | Anti-ctla-4 antibodies and methods of use thereof |
JP7106538B2 (en) | 2016-12-07 | 2022-07-26 | アジェナス インコーポレイテッド | Antibodies and methods of their use |
JP2020511937A (en) | 2016-12-07 | 2020-04-23 | ジェネンテック, インコーポレイテッド | Anti-TAU antibody and method of use |
GB201621635D0 (en) | 2016-12-19 | 2017-02-01 | Ucb Biopharma Sprl | Crystal structure |
AU2017381656B2 (en) | 2016-12-21 | 2020-07-02 | F. Hoffmann-La Roche Ag | Re-use of enzymes in in vitro glycoengineering of antibodies |
EP3559249A1 (en) | 2016-12-21 | 2019-10-30 | H. Hoffnabb-La Roche Ag | Method for in vitro glycoengineering of antibodies |
AU2017384276B9 (en) | 2016-12-21 | 2020-11-26 | F. Hoffmann-La Roche Ag | In vitro glycoengineering of antibodies |
US11274157B2 (en) | 2017-01-12 | 2022-03-15 | Eureka Therapeutics, Inc. | Constructs targeting histone H3 peptide/MHC complexes and uses thereof |
MA47362A (en) | 2017-01-30 | 2019-12-04 | Janssen Biotech Inc | ANTI-TNF ANTIBODIES, COMPOSITIONS AND METHODS FOR THE TREATMENT OF ACTIVE PSORIASIC RHEUMATISM |
WO2018147915A1 (en) | 2017-02-07 | 2018-08-16 | Janssen Biotech, Inc. | Anti-tnf antibodies, compositions, and methods for the treatment of active ankylosing spondylitis |
AU2018219283B2 (en) | 2017-02-08 | 2022-05-19 | Bristol-Myers Squibb Company | Modified relaxin polypeptides comprising a pharmacokinetic enhancer and uses thereof |
TWI778018B (en) | 2017-02-10 | 2022-09-21 | 美商建南德克公司 | Anti-tryptase antibodies, compositions thereof, and uses thereof |
US11021535B2 (en) | 2017-02-10 | 2021-06-01 | The United States Of America As Represented By The Secretary, Department Of Health And Human Services | Neutralizing antibodies to plasmodium falciparum circumsporozoite protein and their use |
WO2018152496A1 (en) | 2017-02-17 | 2018-08-23 | The Usa, As Represented By The Secretary, Dept. Of Health And Human Services | Compositions and methods for the diagnosis and treatment of zika virus infection |
WO2018157027A1 (en) | 2017-02-27 | 2018-08-30 | Regeneron Pharmaceuticals, Inc. | Humanized model of kidney and liver disorders |
MX2019010295A (en) | 2017-03-01 | 2019-11-21 | Genentech Inc | Diagnostic and therapeutic methods for cancer. |
US20190071490A1 (en) | 2017-03-02 | 2019-03-07 | Beth Israel Deaconess Medical Center, Inc. | Preventing Post-Ictal Headaches |
JP2020510671A (en) | 2017-03-03 | 2020-04-09 | シアトル ジェネティックス, インコーポレイテッド | Glycan interacting compounds and methods of use |
SG11201908418RA (en) | 2017-03-13 | 2019-10-30 | Poseida Therapeutics Inc | Compositions and methods for selective elimination and replacement of hematopoietic stem cells |
AU2018240375C1 (en) | 2017-03-22 | 2024-02-01 | Ascendis Pharma A/S | Hydrogel cross-linked hyaluronic acid prodrug compositions and methods |
CR20190481A (en) | 2017-03-22 | 2020-01-06 | Genentech Inc | Optimized antibody compositions for treatment of ocular disorders |
AU2018241625A1 (en) | 2017-03-27 | 2019-09-05 | F. Hoffmann-La Roche Ag | Improved antigen binding receptor formats |
JP2020515256A (en) | 2017-03-27 | 2020-05-28 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | Improved antigen binding receptor |
CN110494452B (en) | 2017-04-03 | 2023-08-25 | 豪夫迈·罗氏有限公司 | Antibodies that bind STEAP-1 |
WO2018184965A1 (en) | 2017-04-03 | 2018-10-11 | F. Hoffmann-La Roche Ag | Immunoconjugates of il-2 with an anti-pd-1 and tim-3 bispecific antibody |
PE20191494A1 (en) | 2017-04-03 | 2019-10-21 | Hoffmann La Roche | IMMUNOCONJUGATES OF AN ANTI-PD-1 ANTIBODY WITH A MUTANT IL-2 OR IL-15 |
EP3606955A1 (en) | 2017-04-05 | 2020-02-12 | H. Hoffnabb-La Roche Ag | Bispecific antibodies specifically binding to pd1 and lag3 |
DK3606954T3 (en) | 2017-04-05 | 2022-09-26 | Hoffmann La Roche | Anti-LAG3-antistoffer |
AU2018253176B2 (en) | 2017-04-13 | 2023-02-02 | Agenus Inc. | Anti-CD137 antibodies and methods of use thereof |
WO2018189379A1 (en) | 2017-04-14 | 2018-10-18 | Gamamabs Pharma | Amhrii-binding compounds for preventing or treating cancers |
MX2019012136A (en) | 2017-04-14 | 2020-07-20 | Gamamabs Pharma | Amhrii-binding compounds for preventing or treating lung cancers. |
TW201841656A (en) | 2017-04-21 | 2018-12-01 | 美商建南德克公司 | Use of klk5 antagonists for treatment of a disease |
JP2020517242A (en) | 2017-04-21 | 2020-06-18 | スターテン・バイオテクノロジー・ベー・フェー | Anti-ApoC3 antibody and method of using the same |
US11236151B2 (en) | 2017-04-25 | 2022-02-01 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Antibodies and methods for the diagnosis and treatment of Epstein Barr virus infection |
WO2018200586A1 (en) | 2017-04-26 | 2018-11-01 | Eureka Therapeutics, Inc. | Constructs specifically recognizing glypican 3 and uses thereof |
WO2018200583A1 (en) | 2017-04-26 | 2018-11-01 | Eureka Therapeutics, Inc. | Cells expressing chimeric activating receptors and chimeric stimulating receptors and uses thereof |
US20220135670A1 (en) | 2017-04-27 | 2022-05-05 | Tesaro, Inc. | Antibody agents directed against lymphocyte activation gene-3 (lag-3) and uses thereof |
HUE062927T2 (en) | 2017-05-01 | 2023-12-28 | Agenus Inc | Anti-tigit antibodies and methods of use thereof |
JOP20190256A1 (en) | 2017-05-12 | 2019-10-28 | Icahn School Med Mount Sinai | Newcastle disease viruses and uses thereof |
EP3625251A1 (en) | 2017-05-15 | 2020-03-25 | University Of Rochester | Broadly neutralizing anti-influenza monoclonal antibody and uses thereof |
EP3630835A1 (en) | 2017-05-31 | 2020-04-08 | STCube & Co., Inc. | Antibodies and molecules that immunospecifically bind to btn1a1 and the therapeutic uses thereof |
KR20200024158A (en) | 2017-05-31 | 2020-03-06 | 주식회사 에스티큐브앤컴퍼니 | How to treat cancer using antibodies and molecules that immunospecifically bind to BTN1A1 |
RU2758513C2 (en) | 2017-06-02 | 2021-10-29 | Пфайзер Инк. | Antibodies specific to flt3 and their applications |
SG10202108528QA (en) | 2017-06-02 | 2021-09-29 | Pfizer | Chimeric antigen receptors targeting flt3 |
KR20200026209A (en) | 2017-06-06 | 2020-03-10 | 주식회사 에스티큐브앤컴퍼니 | How to treat cancer using antibodies and molecules that bind BTN1A1 or BTN1A1-ligand |
GB201709379D0 (en) | 2017-06-13 | 2017-07-26 | Univ Leuven Kath | Humanised ADAMTS13 binding antibodies |
WO2018236904A1 (en) | 2017-06-19 | 2018-12-27 | Surface Oncology, Inc. | Combination of anti-cd47 antibodies and cell death-inducing agents, and uses thereof |
US11654135B2 (en) | 2017-06-22 | 2023-05-23 | Moonshot Pharma Llc | Methods for treating colon cancer with compositions comprising amlexanox and immune checkpoint inhibitors |
MA49565A (en) | 2017-07-11 | 2020-05-20 | Compass Therapeutics Llc | AGONIST ANTIBODIES THAT BIND HUMAN CD137 AND THEIR USES |
WO2019018629A1 (en) | 2017-07-19 | 2019-01-24 | The Usa, As Represented By The Secretary, Dept. Of Health And Human Services | Antibodies and methods for the diagnosis and treatment of hepatitis b virus infection |
WO2019018647A1 (en) | 2017-07-20 | 2019-01-24 | Pfizer Inc. | Anti-gd3 antibodies and antibody-drug conjugates |
JP2020527351A (en) | 2017-07-21 | 2020-09-10 | ジェネンテック, インコーポレイテッド | Cancer treatment and diagnosis |
LT3661954T (en) | 2017-08-03 | 2022-04-11 | Amgen Inc. | Interleukin-21 muteins and methods of treatment |
MA47691A (en) | 2017-08-03 | 2020-01-08 | Alector Llc | ANTI-CD33 ANTIBODIES AND PROCESSES FOR USE |
EP3684811A2 (en) | 2017-08-17 | 2020-07-29 | Massachusetts Institute of Technology | Multiple specificity binders of cxc chemokines and uses thereof |
SG11202000387YA (en) | 2017-08-25 | 2020-03-30 | Five Prime Therapeutics Inc | B7-h4 antibodies and methods of use thereof |
US20210130845A1 (en) | 2017-09-08 | 2021-05-06 | Poseida Therapeutics, Inc. | Compositions and methods for chimeric ligand receptor (clr)-mediated conditional gene expression |
EP3679040B1 (en) | 2017-09-08 | 2022-08-03 | Amgen Inc. | Inhibitors of kras g12c and methods of using the same |
TW201922780A (en) | 2017-09-25 | 2019-06-16 | 美商健生生物科技公司 | Safe and effective method of treating Lupus with anti-IL12/IL23 antibody |
WO2019067499A1 (en) | 2017-09-27 | 2019-04-04 | Alexion Pharmaceuticals, Inc. | Biomarker signature for predicting tumor response to anti-cd200 therapy |
SG10202007194PA (en) | 2017-09-29 | 2020-08-28 | Chugai Pharmaceutical Co Ltd | Multispecific antigen-binding molecules having blood coagulation factor viii (fviii) cofactor function-substituting activity and pharmaceutical formulations containing such a molecule as an active ing |
WO2019073069A1 (en) | 2017-10-13 | 2019-04-18 | Boehringer Ingelheim International Gmbh | Human antibodies to thomsen-nouvelle (tn) antigen |
TW201922294A (en) | 2017-10-31 | 2019-06-16 | 美商伊繆諾金公司 | Combination treatment with antibody-drug conjugates and cytarabine |
US11718679B2 (en) | 2017-10-31 | 2023-08-08 | Compass Therapeutics Llc | CD137 antibodies and PD-1 antagonists and uses thereof |
US20190125799A1 (en) | 2017-10-31 | 2019-05-02 | Allogene Therapeutics, Inc. | Methods and compositions for dosing of allogeneic chimeric antigen receptor t cells |
AU2018361957B2 (en) | 2017-10-31 | 2023-05-25 | Staten Biotechnology B.V. | Anti-ApoC3 antibodies and methods of use thereof |
EP3704150A1 (en) | 2017-11-01 | 2020-09-09 | F. Hoffmann-La Roche AG | The compbody - a multivalent target binder |
JP7092881B2 (en) | 2017-11-01 | 2022-06-28 | エフ.ホフマン-ラ ロシュ アーゲー | TriFab Contour Body |
MX2020004567A (en) | 2017-11-06 | 2020-08-13 | Genentech Inc | Diagnostic and therapeutic methods for cancer. |
WO2019094595A2 (en) | 2017-11-09 | 2019-05-16 | Pinteon Therapeutics Inc. | Methods and compositions for the generation and use of humanized conformation-specific phosphorylated tau antibodies |
WO2019100052A2 (en) | 2017-11-20 | 2019-05-23 | Compass Therapeutics Llc | Cd137 antibodies and tumor antigen-targeting antibodies and uses thereof |
JP7165193B2 (en) | 2017-11-27 | 2022-11-02 | パーデュー、ファーマ、リミテッド、パートナーシップ | Humanized antibody targeting human tissue factor |
US20210087267A1 (en) | 2017-12-20 | 2021-03-25 | Alexion Pharmaceuticals, Inc. | Liquid formulations of anti-cd200 antibodies |
US11802154B2 (en) | 2017-12-20 | 2023-10-31 | Alexion Pharmaceuticals, Inc. | Humanized anti-CD200 antibodies and uses thereof |
JP2021508246A (en) | 2017-12-21 | 2021-03-04 | エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト | CAR-T cell assay for specificity testing of novel antigen binding moiety |
PE20201149A1 (en) | 2017-12-21 | 2020-10-26 | Hoffmann La Roche | HLA-A2 / WT1 BINDING ANTIBODIES |
CN111247429A (en) | 2017-12-21 | 2020-06-05 | 豪夫迈·罗氏有限公司 | Universal reporter cell assay for specific testing of novel antigen binding modules |
EP3728321A1 (en) | 2017-12-22 | 2020-10-28 | F. Hoffmann-La Roche AG | Use of pilra binding agents for treatment of a disease |
SG11202004806SA (en) | 2017-12-22 | 2020-06-29 | Jounce Therapeutics Inc | Antibodies to lilrb2 |
CN111542543B (en) | 2017-12-28 | 2023-12-22 | 南京传奇生物科技有限公司 | Antibodies to PD-L1 and variants thereof |
JP7369127B2 (en) | 2017-12-28 | 2023-10-25 | ナンジン レジェンド バイオテック カンパニー,リミテッド | Single domain antibodies against TIGIT and variants thereof |
WO2019133512A1 (en) | 2017-12-29 | 2019-07-04 | Alector Llc | Anti-tmem106b antibodies and methods of use thereof |
KR20200110358A (en) | 2018-01-12 | 2020-09-23 | 암젠 인크 | Anti-PD-1 Antibodies and Methods of Treatment |
CN111770936A (en) | 2018-01-12 | 2020-10-13 | 百时美施贵宝公司 | Combination therapy of anti-IL-8 and anti-PD-1 antibodies for the treatment of cancer |
WO2019137541A1 (en) | 2018-01-15 | 2019-07-18 | Nanjing Legend Biotech Co., Ltd. | Single-domain antibodies and variants thereof against pd-1 |
US20200339686A1 (en) | 2018-01-16 | 2020-10-29 | Lakepharma, Inc. | Bispecific antibody that binds cd3 and another target |
WO2019152715A1 (en) | 2018-01-31 | 2019-08-08 | Alector Llc | Anti-ms4a4a antibodies and methods of use thereof |
US11396551B2 (en) | 2018-02-01 | 2022-07-26 | Pfizer Inc. | Chimeric antigen receptors targeting CD70 |
EP3746482A1 (en) | 2018-02-01 | 2020-12-09 | Pfizer Inc | Antibodies specific for cd70 and their uses |
WO2019150309A1 (en) | 2018-02-02 | 2019-08-08 | Hammack Scott | Modulators of gpr68 and uses thereof for treating and preventing diseases |
AU2019218786A1 (en) | 2018-02-07 | 2020-07-30 | Dana-Farber Cancer Institute, Inc. | Cell-permeable stapled peptide modules for cellular delivery |
MA51793A (en) | 2018-02-08 | 2020-12-16 | Hoffmann La Roche | BISPECIFIC ANTIGEN BINDING MOLECULES AND METHODS OF USE |
CR20200341A (en) | 2018-02-09 | 2020-11-02 | Hoffmann La Roche | Antibodies binding to gprc5d |
EP3749362A1 (en) | 2018-02-09 | 2020-12-16 | F. Hoffmann-La Roche AG | Therapeutic and diagnostic methods for mast cell-mediated inflammatory diseases |
WO2019160976A1 (en) | 2018-02-14 | 2019-08-22 | Viela Bio, Inc. | Antibodies to feline mcdonough sarcoma (fms)-like tyrosine kinase 3 receptor ligand (flt3l) and uses thereof for treating autoimmune and inflammatory diseases |
GB201802486D0 (en) | 2018-02-15 | 2018-04-04 | Ucb Biopharma Sprl | Methods |
TW202000702A (en) | 2018-02-26 | 2020-01-01 | 美商建南德克公司 | Dosing for treatment with anti-TIGIT and anti-PD-L1 antagonist antibodies |
CN111742219A (en) | 2018-03-01 | 2020-10-02 | 豪夫迈·罗氏有限公司 | Specific assays for novel target antigen binding modules |
WO2019169212A1 (en) | 2018-03-02 | 2019-09-06 | Five Prime Therapeutics, Inc. | B7-h4 antibodies and methods of use thereof |
CA3092551A1 (en) | 2018-03-05 | 2019-09-12 | Janssen Biotech, Inc. | Methods of treating crohn's disease with anti-il23 specific antibody |
BR112020018480B1 (en) | 2018-03-14 | 2022-09-27 | Surface Oncology, Inc | USES OF ANTIBODIES THAT BIND CD39 IN THE TREATMENT OF CANCER |
US20200040103A1 (en) | 2018-03-14 | 2020-02-06 | Genentech, Inc. | Anti-klk5 antibodies and methods of use |
US11891432B2 (en) | 2018-03-15 | 2024-02-06 | Chugai Seiyaku Kabushiki Kaisha | Anti-dengue virus antibodies having cross-reactivity to Zika virus and methods of use |
MA52094A (en) | 2018-03-22 | 2021-01-27 | Adimab Llc | ANTI-IL-27 ANTIBODIES AND THEIR USES |
WO2019190877A1 (en) | 2018-03-26 | 2019-10-03 | Alexion Pharmaceuticals, Inc. | High throughput method for measuring the protease activity of complement c3 convertase |
TWI790370B (en) | 2018-04-02 | 2023-01-21 | 美商必治妥美雅史谷比公司 | Anti-trem-1 antibodies and uses thereof |
US11840568B2 (en) | 2018-04-02 | 2023-12-12 | Mab-Venture Biopharm Co., Ltd. | Lymphocyte activation gene-3 (LAG-3) binding antibody and use thereof |
TW202011029A (en) | 2018-04-04 | 2020-03-16 | 美商建南德克公司 | Methods for detecting and quantifying FGF21 |
CN112424601A (en) | 2018-04-04 | 2021-02-26 | 豪夫迈·罗氏有限公司 | Diagnostic assay for detecting tumor antigens in cancer patients |
JP7394067B2 (en) | 2018-04-04 | 2023-12-07 | エフ・ホフマン-ラ・ロシュ・アクチェンゲゼルシャフト | Diagnostic assays for detecting tumor antigens in cancer patients |
WO2019200357A1 (en) | 2018-04-12 | 2019-10-17 | Surface Oncology, Inc. | Biomarker for cd47 targeting therapeutics and uses therefor |
AR115052A1 (en) | 2018-04-18 | 2020-11-25 | Hoffmann La Roche | MULTI-SPECIFIC ANTIBODIES AND THE USE OF THEM |
AR114789A1 (en) | 2018-04-18 | 2020-10-14 | Hoffmann La Roche | ANTI-HLA-G ANTIBODIES AND THE USE OF THEM |
EP3784274A1 (en) | 2018-04-27 | 2021-03-03 | Fondazione Ebri Rita Levi-Montalcini | Antibody directed against a tau-derived neurotoxic peptide and uses thereof |
WO2019213384A1 (en) | 2018-05-03 | 2019-11-07 | University Of Rochester | Anti-influenza neuraminidase monoclonal antibodies and uses thereof |
MA52590A (en) | 2018-05-11 | 2021-03-17 | Janssen Biotech Inc | METHODS OF TREATING DEPRESSION USING IL-23 ANTIBODIES |
US20210171647A1 (en) | 2018-05-11 | 2021-06-10 | Wuxi Biologics (Shanghai) Co., Ltd. | Fully human antibodies against ox40, method for preparing the same, and use thereof |
WO2019222130A1 (en) | 2018-05-15 | 2019-11-21 | Immunogen, Inc. | Combination treatment with antibody-drug conjugates and flt3 inhibitors |
WO2019226658A1 (en) | 2018-05-21 | 2019-11-28 | Compass Therapeutics Llc | Multispecific antigen-binding compositions and methods of use |
US20200109195A1 (en) | 2018-05-21 | 2020-04-09 | Compass Therapeutics Llc | Compositions and methods for enhancing the killing of target cells by nk cells |
MX2020012607A (en) | 2018-05-23 | 2021-01-29 | Pfizer | Antibodies specific for gucy2c and uses thereof. |
US11434292B2 (en) | 2018-05-23 | 2022-09-06 | Pfizer Inc. | Antibodies specific for CD3 and uses thereof |
BR112020023844A2 (en) | 2018-05-25 | 2021-04-13 | Alector Llc | ANTIBODIES, CANCER TREATMENT METHODS AND PRODUCTION OF AN ANTIBODY, NUCLEIC ACID, VECTOR, HOST CELLS AND PHARMACEUTICAL COMPOSITION |
US11830582B2 (en) | 2018-06-14 | 2023-11-28 | University Of Miami | Methods of designing novel antibody mimetics for use in detecting antigens and as therapeutic agents |
MX2020013808A (en) | 2018-06-18 | 2021-05-27 | UCB Biopharma SRL | Gremlin-1 antagonist for the prevention and treatment of cancer. |
CN112533629A (en) | 2018-06-19 | 2021-03-19 | 阿尔莫生物科技股份有限公司 | Compositions and methods for combined use of IL-10 agents with chimeric antigen receptor cell therapy |
TW202016144A (en) | 2018-06-21 | 2020-05-01 | 日商第一三共股份有限公司 | Compositions including cd3 antigen binding fragments and uses thereof |
MX2020014091A (en) | 2018-06-23 | 2021-05-27 | Genentech Inc | Methods of treating lung cancer with a pd-1 axis binding antagonist, a platinum agent, and a topoisomerase ii inhibitor. |
WO2020006374A2 (en) | 2018-06-29 | 2020-01-02 | Alector Llc | Anti-sirp-beta1 antibodies and methods of use thereof |
PL3618928T3 (en) | 2018-07-13 | 2023-05-02 | Alector Llc | Anti-sortilin antibodies and methods of use thereof |
BR112021000673A2 (en) | 2018-07-18 | 2021-04-20 | Genentech, Inc. | methods for treating an individual with lung cancer, kits, anti-pd-l1 antibody and compositions |
EP3824295A4 (en) | 2018-07-18 | 2022-04-27 | Janssen Biotech, Inc. | Sustained response predictors after treatment with anti-il23 specific antibody |
JP2021531007A (en) | 2018-07-20 | 2021-11-18 | ピエール、ファーブル、メディカマン | Receptor for VISTA |
EP3833442A2 (en) | 2018-08-09 | 2021-06-16 | Compass Therapeutics LLC | Antibodies that bind cd277 and uses thereof |
EP3833443A1 (en) | 2018-08-09 | 2021-06-16 | Compass Therapeutics LLC | Antigen binding agents that bind cd277 and uses thereof |
WO2020033925A2 (en) | 2018-08-09 | 2020-02-13 | Compass Therapeutics Llc | Antibodies that bind cd277 and uses thereof |
AR114550A1 (en) | 2018-08-10 | 2020-09-16 | Chugai Pharmaceutical Co Ltd | ANTI-CD137 ANTIGEN BINDING MOLECULES AND THEIR USES |
MX2021001672A (en) | 2018-08-10 | 2021-07-15 | Eutilex Co Ltd | Chimeric antigen receptor binding to hla-dr, and car-t cell. |
US11548938B2 (en) | 2018-08-21 | 2023-01-10 | Quidel Corporation | DbpA antibodies and uses thereof |
CN113801229A (en) | 2018-08-31 | 2021-12-17 | 艾利妥 | anti-CD 33 antibodies and methods of use thereof |
GB201814281D0 (en) | 2018-09-03 | 2018-10-17 | Femtogenix Ltd | Cytotoxic agents |
US10899826B1 (en) | 2018-09-13 | 2021-01-26 | Teva Pharmaceuticals International Gmbh | Pharmaceutical compositions for an anti-CGRP antagonist antibody |
WO2020061060A1 (en) | 2018-09-19 | 2020-03-26 | Genentech, Inc. | Therapeutic and diagnostic methods for bladder cancer |
MX2021003213A (en) | 2018-09-21 | 2021-05-12 | Genentech Inc | Diagnostic methods for triple-negative breast cancer. |
KR20230148273A (en) | 2018-09-24 | 2023-10-24 | 얀센 바이오테크 인코포레이티드 | Safe and effective method of treating ulcerative colitis with anti-IL12/IL23 antibody |
AU2019352017A1 (en) | 2018-10-03 | 2021-05-06 | Staten Biotechnology B.V. | Antibodies specific for human and cynomolgus ApoC3 and methods of use thereof |
US20210395391A1 (en) | 2018-10-11 | 2021-12-23 | Pfizer Inc. | Dosage Regimen for TFPI Antagonists |
WO2020081767A1 (en) | 2018-10-18 | 2020-04-23 | Genentech, Inc. | Diagnostic and therapeutic methods for sarcomatoid kidney cancer |
GB201817309D0 (en) | 2018-10-24 | 2018-12-05 | Ucb Biopharma Sprl | Antibodies |
GB201817311D0 (en) | 2018-10-24 | 2018-12-05 | Ucb Biopharma Sprl | Antibodies |
EP3870235A1 (en) | 2018-10-24 | 2021-09-01 | F. Hoffmann-La Roche AG | Conjugated chemical inducers of degradation and methods of use |
SG11202104104VA (en) | 2018-11-05 | 2021-05-28 | Genentech Inc | Methods of producing two chain proteins in prokaryotic host cells |
SG11202105010UA (en) | 2018-11-16 | 2021-06-29 | Memorial Sloan Kettering Cancer Center | Antibodies to mucin-16 and methods of use thereof |
WO2020104943A2 (en) | 2018-11-20 | 2020-05-28 | Janssen Biotech, Inc. | Safe and effective method of treating psoriasis with anti-il-23 specific antibody |
JP2022507836A (en) | 2018-11-20 | 2022-01-18 | タケダ ワクチン,インコーポレイテッド | New anti-Zika virus antibody and its use |
WO2020118011A1 (en) | 2018-12-06 | 2020-06-11 | Alexion Pharmaceuticals, Inc. | Anti-alk2 antibodies and uses thereof |
KR20210100668A (en) | 2018-12-06 | 2021-08-17 | 제넨테크, 인크. | Combination therapy of diffuse large B-cell lymphoma comprising an anti-CD79b immunoconjugate, an alkylating agent and an anti-CD20 antibody |
JP2022513198A (en) | 2018-12-10 | 2022-02-07 | ジェネンテック, インコーポレイテッド | Photocrosslinkable peptide for site-specific conjugation to Fc-containing proteins |
US20200197517A1 (en) | 2018-12-18 | 2020-06-25 | Janssen Biotech, Inc. | Safe and Effective Method of Treating Lupus with Anti-IL12/IL23 Antibody |
US20220089694A1 (en) | 2018-12-20 | 2022-03-24 | The U.S.A., As Represented By The Secretary, Department Of Health And Human Services | Ebola virus glycoprotein-specific monoclonal antibodies and uses thereof |
KR20210105947A (en) | 2018-12-20 | 2021-08-27 | 포세이다 테라퓨틱스, 인크. | Nanotransposon compositions and methods of use |
JP2022514290A (en) | 2018-12-20 | 2022-02-10 | ジェネンテック, インコーポレイテッド | Modified antibody FC and usage |
JP2022514082A (en) | 2018-12-21 | 2022-02-09 | ジェネンテック, インコーポレイテッド | Methods of Producing Polypeptides Using Cell Lines Resistant to Apoptosis |
PE20211294A1 (en) | 2018-12-21 | 2021-07-20 | Hoffmann La Roche | ANTIBODY JOINING VEGF AND IL-1BETA AND METHODS OF USE |
WO2020136060A1 (en) | 2018-12-28 | 2020-07-02 | F. Hoffmann-La Roche Ag | A peptide-mhc-i-antibody fusion protein for therapeutic use in a patient with amplified immune response |
KR20210111792A (en) | 2018-12-28 | 2021-09-13 | 스팍스 테라퓨틱스 인크. | Binding molecules specific for claudin 18.2, compositions and methods thereof for treating cancer and other diseases |
AU2020208828A1 (en) | 2019-01-15 | 2021-08-05 | Janssen Biotech, Inc. | Anti-TNF antibody compositions and methods for the treatment of juvenile idiopathic arthritis |
EP3911679A1 (en) | 2019-01-16 | 2021-11-24 | Compass Therapeutics LLC | Formulations of antibodies that bind human cd137 and uses thereof |
GB201900732D0 (en) | 2019-01-18 | 2019-03-06 | Ucb Biopharma Sprl | Antibodies |
EP3914618A1 (en) | 2019-01-23 | 2021-12-01 | Janssen Biotech, Inc. | Anti-tnf antibody compositions for use in methods for the treatment of psoriatic arthritis |
WO2020154410A1 (en) | 2019-01-23 | 2020-07-30 | Genentech, Inc. | Methods of producing multimeric proteins in eukaryotic host cells |
WO2020153467A1 (en) | 2019-01-24 | 2020-07-30 | 中外製薬株式会社 | Novel cancer antigens and antibodies of said antigens |
US20220073600A1 (en) | 2019-01-28 | 2022-03-10 | Maple Biotech Llc | Methods for treating disease using psmp antagonists |
GB201901197D0 (en) | 2019-01-29 | 2019-03-20 | Femtogenix Ltd | G-A Crosslinking cytotoxic agents |
MA55080A (en) | 2019-02-26 | 2022-01-05 | Inspirna Inc | HIGH AFFINITY ANTI-MERTK ANTIBODIES AND ASSOCIATED USES |
AU2020228383A1 (en) | 2019-02-27 | 2021-09-23 | Genentech, Inc. | Dosing for treatment with anti-tigit and anti-CD20 or anti-CD38 antibodies |
TW202101000A (en) | 2019-03-08 | 2021-01-01 | 美商建南德克公司 | Methods for detecting and quantifying membrane-associated proteins |
US20220144934A1 (en) | 2019-03-14 | 2022-05-12 | Janssen Biotech, Inc. | Methods for Producing Anti-TNF Antibody Compositions |
EA202192508A1 (en) | 2019-03-14 | 2022-03-29 | Янссен Байотек, Инк. | METHODS FOR OBTAINING COMPOSITIONS OF ANTIBODIES TO TNF |
US20220153830A1 (en) | 2019-03-14 | 2022-05-19 | Janssen Biotech, Inc. | Manufacturing Methods for Producing Anti-TNF Antibody Compositions |
EP3938384A4 (en) | 2019-03-14 | 2022-12-28 | Janssen Biotech, Inc. | Manufacturing methods for producing anti-il12/il23 antibody compositions |
WO2020188466A1 (en) | 2019-03-18 | 2020-09-24 | Janssen Biotech, Inc. | Method of treating psoriasis in pediatric subjects with anti-il12/il23 antibody |
US20220169706A1 (en) | 2019-03-28 | 2022-06-02 | Danisco Us Inc | Engineered antibodies |
SG11202109510YA (en) | 2019-03-29 | 2021-10-28 | Genentech Inc | Modulators of cell surface protein interactions and methods and compositions related to same |
CN114364703A (en) | 2019-04-19 | 2022-04-15 | 豪夫迈·罗氏有限公司 | Anti-merk antibodies and methods of use thereof |
US20220227853A1 (en) | 2019-05-03 | 2022-07-21 | The United States Of America,As Represented By The Secretary,Department Of Health And Human Services | Neutralizing antibodies to plasmodium falciparum circumsporozoite protein and their use |
TW202108178A (en) | 2019-05-14 | 2021-03-01 | 美商建南德克公司 | METHODS OF USING ANTI-CD79b IMMUNOCONJUGATES TO TREAT FOLLICULAR LYMPHOMA |
US20230085439A1 (en) | 2019-05-21 | 2023-03-16 | University Of Georgia Research Foundation, Inc. | Antibodies that bind human metapneumovirus fusion protein and their use |
CA3138241A1 (en) | 2019-05-23 | 2020-11-26 | Janssen Biotech, Inc. | Method of treating inflammatory bowel disease with a combination therapy of antibodies to il-23 and tnf alpha |
CA3141531A1 (en) | 2019-05-24 | 2020-12-03 | Pfizer Inc. | Combination therapies using cdk inhibitors |
CN113939531A (en) | 2019-06-03 | 2022-01-14 | 詹森生物科技公司 | anti-TNF antibody compositions and methods for treating psoriatic arthritis |
CA3142580A1 (en) | 2019-06-03 | 2020-12-10 | Janssen Biotech, Inc. | Anti-tnf antibodies, compositions, and methods for the treatment of active ankylosing spondylitis |
US20200392229A1 (en) | 2019-06-11 | 2020-12-17 | Alector Llc | Methods of use of anti-sortilin antibodies |
CN114051500A (en) | 2019-07-02 | 2022-02-15 | 豪夫迈·罗氏有限公司 | Immunoconjugates comprising interleukin-2 mutants and anti-CD 8 antibodies |
AR119393A1 (en) | 2019-07-15 | 2021-12-15 | Hoffmann La Roche | ANTIBODIES THAT BIND NKG2D |
CN114144436A (en) | 2019-07-24 | 2022-03-04 | H.隆德贝克有限公司 | anti-mGluR 5 antibodies and uses thereof |
CN114341181A (en) | 2019-07-31 | 2022-04-12 | 艾莱克特有限责任公司 | anti-MS 4A4A antibodies and methods of use thereof |
JP2022543551A (en) | 2019-07-31 | 2022-10-13 | エフ・ホフマン-ラ・ロシュ・アクチェンゲゼルシャフト | Antibody that binds to GPRC5D |
CR20220019A (en) | 2019-07-31 | 2022-02-11 | Hoffmann La Roche | Antibodies binding to gprc5d |
CN114641490B (en) | 2019-08-06 | 2023-06-06 | 新旭生技股份有限公司 | Antibodies that bind to pathological TAU species and uses thereof |
TW202120551A (en) | 2019-08-12 | 2021-06-01 | 美商普瑞諾生物科技公司 | Methods and compositions for promoting and potentiating t‐cell mediated immune responses through adcc targeting of cd39 expressing cells |
BR112022002761A2 (en) | 2019-08-12 | 2022-08-09 | Aptevo Res & Development Llc | 4-1BB AND OX40 BINDING PROTEINS AND RELATED COMPOSITIONS AND METHODS, 4-1BB ANTIBODIES, OX40 ANTIBODIES |
WO2021028752A1 (en) | 2019-08-15 | 2021-02-18 | Janssen Biotech, Inc. | Anti-tfn antibodies for treating type i diabetes |
JP2022545741A (en) | 2019-08-30 | 2022-10-28 | アジェナス インコーポレイテッド | ANTI-CD96 ANTIBODY AND METHODS OF USE THEREOF |
US20220306736A1 (en) | 2019-09-04 | 2022-09-29 | Y-Biologics Inc. | Anti-vsig4 antibody or antigen binding fragment and uses thereof |
WO2021046261A1 (en) | 2019-09-05 | 2021-03-11 | Poseida Therapeutics, Inc. | Allogeneic cell compositions and methods of use |
MX2022002963A (en) | 2019-09-12 | 2022-04-06 | Genentech Inc | Compositions and methods of treating lupus nephritis. |
BR112022002351A2 (en) | 2019-09-16 | 2022-07-19 | Surface Oncology Inc | ANTI-CD39 ANTIBODY COMPOSITIONS AND METHODS |
CA3150999A1 (en) | 2019-09-18 | 2021-03-25 | James Thomas Koerber | Anti-klk7 antibodies, anti-klk5 antibodies, multispecific anti-klk5/klk7 antibodies, and methods of use |
CR20220149A (en) | 2019-09-20 | 2022-05-23 | Genentech Inc | Dosing for anti-tryptase antibodies |
US20210115127A1 (en) | 2019-09-25 | 2021-04-22 | Surface Oncology, Inc. | Anti-il-27 antibodies and uses thereof |
US20220411511A1 (en) | 2019-09-26 | 2022-12-29 | Stcube & Co. | Antibodies specific to glycosylated ctla-4 and methods of use thereof |
CN114829401A (en) | 2019-09-27 | 2022-07-29 | 南京金斯瑞生物科技有限公司 | anti-VHH domain antibodies and uses thereof |
US11760801B2 (en) | 2019-09-27 | 2023-09-19 | Janssen Biotech, Inc. | Anti-CEACAM antibodies and uses thereof |
CA3151406A1 (en) | 2019-09-27 | 2021-04-01 | Raymond D. Meng | Dosing for treatment with anti-tigit and anti-pd-l1 antagonist antibodies |
US20220356248A1 (en) | 2019-10-09 | 2022-11-10 | Stcube & Co | Antibodies specific to glycosylated lag3 and methods of use thereof |
TW202122114A (en) | 2019-10-18 | 2021-06-16 | 美商建南德克公司 | Methods of using anti-cd79b immunoconjugates to treat diffuse large b-cell lymphoma |
EP3812008A1 (en) | 2019-10-23 | 2021-04-28 | Gamamabs Pharma | Amh-competitive antagonist antibody |
US11459389B2 (en) | 2019-10-24 | 2022-10-04 | Massachusetts Institute Of Technology | Monoclonal antibodies that bind human CD161 |
IL292458A (en) | 2019-11-06 | 2022-06-01 | Genentech Inc | Diagnostic and therapeutic methods for treatment of hematologic cancers |
GB201917480D0 (en) | 2019-11-29 | 2020-01-15 | Univ Oxford Innovation Ltd | Antibodies |
CR20230210A (en) | 2019-12-13 | 2023-06-14 | Genentech Inc | Anti-ly6g6d antibodies and methods of use |
BR112022011570A2 (en) | 2019-12-13 | 2022-12-13 | Alector Llc | ANTI-MERTK ANTIBODIES AND METHODS OF THEIR USE |
EP4076666A1 (en) | 2019-12-18 | 2022-10-26 | F. Hoffmann-La Roche AG | Antibodies binding to hla-a2/mage-a4 |
CA3161024A1 (en) | 2019-12-19 | 2021-06-24 | Quidel Corporation | Monoclonal antibody fusions |
GB201919062D0 (en) | 2019-12-20 | 2020-02-05 | Ucb Biopharma Sprl | Antibody |
JP2023510121A (en) | 2019-12-20 | 2023-03-13 | ポセイダ セラピューティクス,インコーポレイティド | Anti-Muc1 compositions and methods of use |
GB201919058D0 (en) | 2019-12-20 | 2020-02-05 | Ucb Biopharma Sprl | Multi-specific antibodies |
GB201919061D0 (en) | 2019-12-20 | 2020-02-05 | Ucb Biopharma Sprl | Multi-specific antibody |
MX2022007840A (en) | 2019-12-27 | 2022-07-19 | Chugai Pharmaceutical Co Ltd | Anti-ctla-4 antibody and use thereof. |
TW202138388A (en) | 2019-12-30 | 2021-10-16 | 美商西根公司 | Methods of treating cancer with nonfucosylated anti-cd70 antibodies |
CN114929278A (en) | 2020-01-06 | 2022-08-19 | 瓦西尼斯公司 | anti-CCR 8 antibodies and uses thereof |
CN110818795B (en) | 2020-01-10 | 2020-04-24 | 上海复宏汉霖生物技术股份有限公司 | anti-TIGIT antibodies and methods of use |
JP2023511274A (en) | 2020-01-14 | 2023-03-17 | シンセカイン インコーポレイテッド | IL2 orthologs and usage |
WO2022050954A1 (en) | 2020-09-04 | 2022-03-10 | Genentech, Inc. | Dosing for treatment with anti-tigit and anti-pd-l1 antagonist antibodies |
WO2021194481A1 (en) | 2020-03-24 | 2021-09-30 | Genentech, Inc. | Dosing for treatment with anti-tigit and anti-pd-l1 antagonist antibodies |
CN115427453A (en) | 2020-02-10 | 2022-12-02 | 上海诗健生物科技有限公司 | CLDN18.2 antibodies and uses thereof |
AU2021218927A1 (en) | 2020-02-10 | 2022-09-22 | Shanghai Escugen Biotechnology Co., Ltd. | Claudin 18.2 antibody and use thereof |
TW202144395A (en) | 2020-02-12 | 2021-12-01 | 日商中外製藥股份有限公司 | Anti-CD137 antigen-binding molecule for use in cancer treatment |
US20230096030A1 (en) | 2020-02-13 | 2023-03-30 | UCB Biopharma SRL | Bispecific antibodies against cd9 and cd7 |
EP4103612A1 (en) | 2020-02-13 | 2022-12-21 | UCB Biopharma SRL | Bispecific antibodies against cd9 |
US20230192900A1 (en) | 2020-02-13 | 2023-06-22 | UCB Biopharma SRL | Bispecific antibodies binding hvem and cd9 |
US20230151108A1 (en) | 2020-02-13 | 2023-05-18 | UCB Biopharma SRL | Bispecific antibodies against cd9 and cd137 |
US20230125234A1 (en) | 2020-02-13 | 2023-04-27 | UCB Biopharma SRL | Anti cd44-ctla4 bispecific antibodies |
CA3169451A1 (en) | 2020-02-14 | 2021-08-19 | Jounce Therapeutics, Inc. | Antibodies and fusion proteins that bind to ccr8 and uses thereof |
JP2023513834A (en) | 2020-02-18 | 2023-04-03 | アレクトル エルエルシー | PILRA antibody and method of use thereof |
KR20220145859A (en) | 2020-02-28 | 2022-10-31 | 상하이 헨리우스 바이오테크, 인크. | Anti-CD137 constructs, multispecific antibodies and uses thereof |
AU2021225920A1 (en) | 2020-02-28 | 2022-09-15 | Shanghai Henlius Biotech, Inc. | Anti-CD137 construct and use thereof |
WO2021176424A1 (en) | 2020-03-06 | 2021-09-10 | Ona Therapeutics, S.L. | Anti-cd36 antibodies and their use to treat cancer |
US11896619B2 (en) | 2020-03-10 | 2024-02-13 | Massachusetts Institute Of Technology | Compositions and methods for immunotherapy of NPM1c-positive cancer |
US20230121433A1 (en) | 2020-03-11 | 2023-04-20 | Poseida Therapeutics, Inc. | Chimeric stimulatory receptors and methods of use in t cell activation and differentiation |
KR20220152262A (en) | 2020-03-13 | 2022-11-15 | 제넨테크, 인크. | Anti-interleukin-33 antibodies and uses thereof |
CA3169626A1 (en) | 2020-03-19 | 2021-09-23 | Genentech, Inc. | Isoform-selective anti-tgf-beta antibodies and methods of use |
JP2023519213A (en) | 2020-03-24 | 2023-05-10 | ジェネンテック, インコーポレイテッド | TIE2 binding agents and methods of use |
WO2021202473A2 (en) | 2020-03-30 | 2021-10-07 | Danisco Us Inc | Engineered antibodies |
EP4126940A1 (en) | 2020-03-30 | 2023-02-08 | F. Hoffmann-La Roche AG | Antibody that binds to vegf and pdgf-b and methods of use |
CN116075525A (en) | 2020-03-31 | 2023-05-05 | 艾莱克特有限责任公司 | anti-MERTK antibodies and methods of use thereof |
JP2023519930A (en) | 2020-04-01 | 2023-05-15 | ユニバーシティ オブ ロチェスター | Monoclonal Antibodies Against Hemagglutinin (HA) and Neuraminidase (NA) of Influenza H3N2 Virus |
WO2021202959A1 (en) | 2020-04-03 | 2021-10-07 | Genentech, Inc. | Therapeutic and diagnostic methods for cancer |
IL297025A (en) | 2020-04-14 | 2022-12-01 | Poseida Therapeutics Inc | Compositions and methods for use in the treatment of cancer |
BR112022020629A2 (en) | 2020-04-15 | 2022-11-29 | Hoffmann La Roche | INTERLEUKIN-7 (IL-7) POLYPEPTIDE, IMMUNOCONJUGATE, ONE OR MORE POLYNUCLEOTIDES ISOLATED, HOST CELL, METHODS FOR PRODUCING AN IL-7 POLYPEPTIDE MUTANT OR AN IMMUNOCONJUGATE, FOR TREAT A DISEASE, AND FOR STIMULATING THE IMMUNE SYSTEM, IL-7 POLYPEPTIDE OR IMMUNOCONJUGATE 7 MUTANT, PHARMACEUTICAL COMPOSITION, USE OF THE IL-7 MUTANT POLYPEPTIDE AND INVENTION |
TW202206111A (en) | 2020-04-24 | 2022-02-16 | 美商建南德克公司 | Methods of using anti-cd79b immunoconjugates |
EP4143345A1 (en) | 2020-04-28 | 2023-03-08 | Genentech, Inc. | Methods and compositions for non-small cell lung cancer immunotherapy |
SG11202112792WA (en) | 2020-04-28 | 2021-12-30 | Univ Rockefeller | Neutralizing anti-sars-cov-2 antibodies and methods of use thereof |
IL297830A (en) | 2020-05-03 | 2023-01-01 | Levena Suzhou Biopharma Co Ltd | Antibody-drug conjugates (adcs) comprising an anti-trop-2 antibody, compositions comprising such adcs, as well as methods of making and using the same |
WO2021226290A1 (en) | 2020-05-05 | 2021-11-11 | 10X Genomics, Inc. | Methods for identification of antigen-binding molecules |
CN115697491A (en) | 2020-05-17 | 2023-02-03 | 阿斯利康(英国)有限公司 | SARS-COV-2 antibodies and methods of selection and use thereof |
US20230220057A1 (en) | 2020-05-27 | 2023-07-13 | Staidson (Beijing) Biopharmaceuticals Co., Ltd. | Antibodies specifically recognizing nerve growth factor and uses thereof |
WO2021247618A1 (en) | 2020-06-02 | 2021-12-09 | 10X Genomics, Inc. | Enrichment of nucleic acid sequences |
CN116529260A (en) | 2020-06-02 | 2023-08-01 | 当康生物技术有限责任公司 | anti-CD 93 constructs and uses thereof |
KR20230037532A (en) | 2020-06-02 | 2023-03-16 | 다이내믹큐어 바이오테크놀로지 엘엘씨 | Anti-CD93 constructs and uses thereof |
CR20220659A (en) | 2020-06-08 | 2023-08-21 | Hoffmann La Roche | Anti-hbv antibodies and methods of use |
GB202008651D0 (en) | 2020-06-09 | 2020-07-22 | Univ Newcastle | Method of identifying complement modulators |
JP2023529206A (en) | 2020-06-12 | 2023-07-07 | ジェネンテック, インコーポレイテッド | Methods and compositions for cancer immunotherapy |
IL299039A (en) | 2020-06-16 | 2023-02-01 | Genentech Inc | Methods and compositions for treating triple-negative breast cancer |
CA3181672A1 (en) | 2020-06-18 | 2021-12-23 | Shi Li | Treatment with anti-tigit antibodies and pd-1 axis binding antagonists |
AU2021308653A1 (en) | 2020-07-17 | 2023-02-16 | Genentech, Inc. | Anti-Notch2 antibodies and methods of use |
CN116323668A (en) | 2020-07-17 | 2023-06-23 | 辉瑞公司 | Therapeutic antibodies and uses thereof |
EP4182343A2 (en) | 2020-07-20 | 2023-05-24 | AstraZeneca UK Limited | Sars-cov-2 proteins, anti-sars-cov-2 antibodies, and methods of using the same |
WO2022020456A2 (en) | 2020-07-21 | 2022-01-27 | Allogene Therapeutics, Inc. | Chimeric antigen receptors with enhanced signaling and activities and uses thereof |
TW202216215A (en) | 2020-07-21 | 2022-05-01 | 美商建南德克公司 | Antibody-conjugated chemical inducers of degradation of brm and methods thereof |
GB2597532A (en) | 2020-07-28 | 2022-02-02 | Femtogenix Ltd | Cytotoxic compounds |
WO2022026763A1 (en) | 2020-07-29 | 2022-02-03 | Dynamicure Biotechnology Llc | Anti-cd93 constructs and uses thereof |
US11725052B2 (en) | 2020-08-18 | 2023-08-15 | Cephalon Llc | Anti-PAR-2 antibodies and methods of use thereof |
KR20230084497A (en) | 2020-09-11 | 2023-06-13 | 메디뮨 리미티드 | Therapeutic B7-H4 binding molecules |
JP2023542301A (en) | 2020-09-12 | 2023-10-06 | メディミューン リミテッド | Scoring method for anti-B7H4 antibody drug conjugate therapy |
EP3981789A1 (en) | 2020-10-12 | 2022-04-13 | Commissariat À L'Énergie Atomique Et Aux Énergies Alternatives | Anti-lilrb antibodies and uses thereof |
EP4229081A1 (en) | 2020-10-15 | 2023-08-23 | The United States of America, as represented by The Secretary, Department of Health and Human Services | Antibody specific for sars-cov-2 receptor binding domain and therapeutic methods |
AU2021359092A1 (en) | 2020-10-15 | 2023-06-01 | UCB Biopharma SRL | Binding molecules that multimerise cd45 |
WO2022084210A1 (en) | 2020-10-20 | 2022-04-28 | F. Hoffmann-La Roche Ag | Combination therapy of pd-1 axis binding antagonists and lrrk2 inhitibors |
WO2022087274A1 (en) | 2020-10-21 | 2022-04-28 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Antibodies that neutralize type-i interferon (ifn) activity |
JP2023547447A (en) | 2020-10-28 | 2023-11-10 | エフ・ホフマン-ラ・ロシュ・アクチェンゲゼルシャフト | Improved antigen binding receptor |
WO2022098638A2 (en) | 2020-11-04 | 2022-05-12 | Genentech, Inc. | Dosing for treatment with anti-cd20/anti-cd3 bispecific antibodies |
AU2021374590A1 (en) | 2020-11-04 | 2023-06-01 | Genentech, Inc. | Subcutaneous dosing of anti-cd20/anti-cd3 bispecific antibodies |
AU2021374594A1 (en) | 2020-11-04 | 2023-06-01 | Genentech, Inc. | Dosing for treatment with anti-cd20/anti-cd3 bispecific antibodies and anti-cd79b antibody drug conjugates |
US11919945B2 (en) | 2020-11-04 | 2024-03-05 | The Rockefeller University | Neutralizing anti-SARS-CoV-2 antibodies |
JP2023551907A (en) | 2020-12-01 | 2023-12-13 | アプティーボ リサーチ アンド デベロップメント エルエルシー | Tumor-associated antigens and CD3 binding proteins, related compositions, and methods |
WO2022120352A1 (en) | 2020-12-02 | 2022-06-09 | Alector Llc | Methods of use of anti-sortilin antibodies |
WO2022118197A1 (en) | 2020-12-02 | 2022-06-09 | Pfizer Inc. | Time to resolution of axitinib-related adverse events |
AU2021395729A1 (en) | 2020-12-07 | 2023-07-13 | UCB Biopharma SRL | Multi-specific antibodies and antibody combinations |
AU2021398385A1 (en) | 2020-12-07 | 2023-07-13 | UCB Biopharma SRL | Antibodies against interleukin-22 |
WO2022132904A1 (en) | 2020-12-17 | 2022-06-23 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Human monoclonal antibodies targeting sars-cov-2 |
CA3204702A1 (en) | 2020-12-17 | 2022-06-23 | F. Hoffmann-La Roche Ag | Anti-hla-g antibodies and use thereof |
WO2022148853A1 (en) | 2021-01-11 | 2022-07-14 | F. Hoffmann-La Roche Ag | Immunoconjugates |
CA3204731A1 (en) | 2021-01-13 | 2022-07-21 | John T. POIRIER | Anti-dll3 antibody-drug conjugate |
WO2022153194A1 (en) | 2021-01-13 | 2022-07-21 | Memorial Sloan Kettering Cancer Center | Antibody-pyrrolobenzodiazepine derivative conjugate |
WO2022155324A1 (en) | 2021-01-15 | 2022-07-21 | The Rockefeller University | Neutralizing anti-sars-cov-2 antibodies |
WO2022173689A1 (en) | 2021-02-09 | 2022-08-18 | University Of Georgia Research Foundation, Inc. | Human monoclonal antibodies against pneumococcal antigens |
JP2024506315A (en) | 2021-02-09 | 2024-02-13 | ザ ユナイテッド ステイツ オブ アメリカ アズ リプリゼンテッド バイ ザ セクレタリー、デパートメント オブ ヘルス アンド ヒューマン サービシーズ | Antibodies that target the coronavirus spike protein |
JP2024509165A (en) | 2021-03-02 | 2024-02-29 | シージーアールピー ダイアグノスティクス ゲーエムベーハー | Treating and/or reducing the occurrence of migraine |
TW202302645A (en) | 2021-03-03 | 2023-01-16 | 法商皮爾法伯製藥公司 | Anti-vsig4 antibody or antigen binding fragment and uses thereof |
CN117440832A (en) | 2021-03-03 | 2024-01-23 | 索伦托药业有限公司 | Antibody-drug conjugates comprising anti-BCMA antibodies |
WO2022187863A1 (en) | 2021-03-05 | 2022-09-09 | Dynamicure Biotechnology Llc | Anti-vista constructs and uses thereof |
KR20230156764A (en) | 2021-03-12 | 2023-11-14 | 얀센 바이오테크 인코포레이티드 | Method for treating psoriatic arthritis patients with inadequate response to TNF therapy by anti-IL23 specific antibody |
AU2022233792A1 (en) | 2021-03-12 | 2023-10-26 | Janssen Biotech, Inc. | Safe and effective method of treating psoriatic arthritis with anti-il23 specific antibody |
CN117062839A (en) | 2021-03-12 | 2023-11-14 | 基因泰克公司 | anti-KLK 7 antibodies, anti-KLK 5 antibodies, multispecific anti-KLK 5/KLK7 antibodies, and methods of use |
AU2022238526A1 (en) | 2021-03-15 | 2023-09-07 | F. Hoffmann-La Roche Ag | Compositions and methods of treating lupus nephritis |
WO2022195028A2 (en) | 2021-03-18 | 2022-09-22 | Medimmune Limited | Therapeutic binding molecules |
CN116981696A (en) | 2021-03-18 | 2023-10-31 | 艾莱克特有限责任公司 | anti-TMEM 106B antibodies and methods of use thereof |
WO2022197877A1 (en) | 2021-03-19 | 2022-09-22 | Genentech, Inc. | Methods and compositions for time delayed bio-orthogonal release of cytotoxic agents |
EP4314063A1 (en) | 2021-03-23 | 2024-02-07 | Alector LLC | Anti-tmem106b antibodies for treating and preventing coronavirus infections |
CN117616041A (en) | 2021-03-25 | 2024-02-27 | 当康生物技术有限责任公司 | anti-IGFBP 7 constructs and uses thereof |
EP4067381A1 (en) | 2021-04-01 | 2022-10-05 | Julius-Maximilians-Universität Würzburg | Novel tnfr2 binding molecules |
AR125344A1 (en) | 2021-04-15 | 2023-07-05 | Chugai Pharmaceutical Co Ltd | ANTI-C1S ANTIBODY |
JP2024509664A (en) | 2021-04-30 | 2024-03-05 | エフ・ホフマン-ラ・ロシュ・アクチェンゲゼルシャフト | Medication for treatment with anti-CD20/anti-CD3 bispecific antibodies |
CN117321078A (en) | 2021-04-30 | 2023-12-29 | 豪夫迈·罗氏有限公司 | Administration for combination therapy with anti-CD 20/anti-CD 3 bispecific antibody and anti-CD 79B antibody drug conjugates |
EP4334355A1 (en) | 2021-05-03 | 2024-03-13 | UCB Biopharma SRL | Antibodies |
EP4334343A2 (en) | 2021-05-06 | 2024-03-13 | The Rockefeller University | Neutralizing anti-sars- cov-2 antibodies and methods of use thereof |
KR20240005809A (en) | 2021-05-07 | 2024-01-12 | 서피스 온콜로지, 엘엘씨 | Anti-IL-27 antibodies and uses thereof |
CA3218170A1 (en) | 2021-05-12 | 2022-11-17 | Jamie Harue HIRATA | Methods of using anti-cd79b immunoconjugates to treat diffuse large b-cell lymphoma |
CN113278071B (en) | 2021-05-27 | 2021-12-21 | 江苏荃信生物医药股份有限公司 | Anti-human interferon alpha receptor1 monoclonal antibody and application thereof |
CA3220629A1 (en) | 2021-05-28 | 2022-12-01 | Tobin J. CAMMETT | Methods for detecting cm-tma biomarkers |
WO2022256313A1 (en) | 2021-06-01 | 2022-12-08 | 10X Genomics, Inc. | Validation of a unique molecular identifier associated with a nucleic acid sequence of interest |
AR126054A1 (en) | 2021-06-04 | 2023-09-06 | Chugai Pharmaceutical Co Ltd | ANTI-DDR2 ANTIBODIES AND USES OF THESE |
BR112023025738A2 (en) | 2021-06-09 | 2024-02-27 | Hoffmann La Roche | COMBINATION OF A BRAF INHIBITOR AND A PD-1 AXIS BINDING ANTAGONIST, USE OF A COMBINATION OF A BRAF INHIBITOR AND A PD-1 AXIS BINDING ANTAGONIST, METHOD FOR THE TREATMENT OR PROPHYLAXIS OF CANCER, PHARMACEUTICAL COMPOSITION AND INVENTION |
WO2022263357A1 (en) | 2021-06-14 | 2022-12-22 | Argenx Iip Bv | Anti-il-9 antibodies and methods of use thereof |
WO2022266223A1 (en) | 2021-06-16 | 2022-12-22 | Alector Llc | Bispecific anti-mertk and anti-pdl1 antibodies and methods of use thereof |
WO2022266221A1 (en) | 2021-06-16 | 2022-12-22 | Alector Llc | Monovalent anti-mertk antibodies and methods of use thereof |
WO2022266660A1 (en) | 2021-06-17 | 2022-12-22 | Amberstone Biosciences, Inc. | Anti-cd3 constructs and uses thereof |
IL309115A (en) | 2021-06-25 | 2024-02-01 | Chugai Pharmaceutical Co Ltd | Anti–ctla-4 antibody |
CN117545779A (en) | 2021-06-25 | 2024-02-09 | 中外制药株式会社 | Use of anti-CTLA-4 antibodies |
TW202317190A (en) | 2021-06-29 | 2023-05-01 | 美商思進公司 | Methods of treating cancer with a combination of a nonfucosylated anti-cd70 antibody and a cd47 antagonist |
WO2023283611A1 (en) | 2021-07-08 | 2023-01-12 | Staidson Biopharma Inc. | Antibodies specifically recognizing tnfr2 and uses thereof |
WO2023281466A1 (en) | 2021-07-09 | 2023-01-12 | Janssen Biotech, Inc. | Manufacturing methods for producing anti-il12/il23 antibody compositions |
AU2022308201A1 (en) | 2021-07-09 | 2024-02-22 | Janssen Biotech, Inc. | Manufacturing methods for producing anti-tnf antibody compositions |
WO2023281462A1 (en) | 2021-07-09 | 2023-01-12 | Janssen Biotech, Inc. | Manufacturing methods for producing anti-tnf antibody compositions |
WO2023285878A1 (en) | 2021-07-13 | 2023-01-19 | Aviation-Ophthalmology | Methods for detecting, treating, and preventing gpr68-mediated ocular diseases, disorders, and conditions |
CN115812082A (en) | 2021-07-14 | 2023-03-17 | 舒泰神(北京)生物制药股份有限公司 | Antibody specifically recognizing CD40 and application thereof |
WO2023004386A1 (en) | 2021-07-22 | 2023-01-26 | Genentech, Inc. | Brain targeting compositions and methods of use thereof |
WO2023001884A1 (en) | 2021-07-22 | 2023-01-26 | F. Hoffmann-La Roche Ag | Heterodimeric fc domain antibodies |
WO2023007472A1 (en) | 2021-07-30 | 2023-02-02 | ONA Therapeutics S.L. | Anti-cd36 antibodies and their use to treat cancer |
WO2023012147A1 (en) | 2021-08-03 | 2023-02-09 | F. Hoffmann-La Roche Ag | Bispecific antibodies and methods of use |
US11807685B2 (en) | 2021-08-05 | 2023-11-07 | The Uab Research Foundation | Anti-CD47 antibody and uses thereof |
CA3227511A1 (en) | 2021-08-06 | 2023-02-09 | Lætitia LINARES | Methods for the treatment of cancer |
WO2023019239A1 (en) | 2021-08-13 | 2023-02-16 | Genentech, Inc. | Dosing for anti-tryptase antibodies |
GB202111905D0 (en) | 2021-08-19 | 2021-10-06 | UCB Biopharma SRL | Antibodies |
WO2023026205A1 (en) | 2021-08-24 | 2023-03-02 | Cgrp Diagnostics Gmbh | Preventative treatment of migraine |
WO2023034750A1 (en) | 2021-08-30 | 2023-03-09 | Genentech, Inc. | Anti-polyubiquitin multispecific antibodies |
CA3230815A1 (en) | 2021-09-03 | 2023-03-09 | University Of Bern | Compositions and methods for treating long ot syndrome |
WO2023056403A1 (en) | 2021-09-30 | 2023-04-06 | Genentech, Inc. | Methods for treatment of hematologic cancers using anti-tigit antibodies, anti-cd38 antibodies, and pd-1 axis binding antagonists |
WO2023060088A1 (en) | 2021-10-04 | 2023-04-13 | Poseida Therapeutics, Inc. | Transposon compositions and methods of use thereof |
TW202327595A (en) | 2021-10-05 | 2023-07-16 | 美商輝瑞大藥廠 | Combinations of azalactam compounds for the treatment of cancer |
WO2023062048A1 (en) | 2021-10-14 | 2023-04-20 | F. Hoffmann-La Roche Ag | Alternative pd1-il7v immunoconjugates for the treatment of cancer |
WO2023062050A1 (en) | 2021-10-14 | 2023-04-20 | F. Hoffmann-La Roche Ag | New interleukin-7 immunoconjugates |
WO2023069919A1 (en) | 2021-10-19 | 2023-04-27 | Alector Llc | Anti-cd300lb antibodies and methods of use thereof |
WO2023073615A1 (en) | 2021-10-29 | 2023-05-04 | Janssen Biotech, Inc. | Methods of treating crohn's disease with anti-il23 specific antibody |
EP4177266A1 (en) | 2021-11-05 | 2023-05-10 | Katholieke Universiteit Leuven | Neutralizing anti-sars-cov-2 human antibodies |
WO2023086807A1 (en) | 2021-11-10 | 2023-05-19 | Genentech, Inc. | Anti-interleukin-33 antibodies and uses thereof |
WO2023086824A1 (en) | 2021-11-10 | 2023-05-19 | 10X Genomics, Inc. | Methods for identification of antigen-binding molecules |
US20230151087A1 (en) | 2021-11-15 | 2023-05-18 | Janssen Biotech, Inc. | Methods of Treating Crohn's Disease with Anti-IL23 Specific Antibody |
WO2023091887A1 (en) | 2021-11-16 | 2023-05-25 | Genentech, Inc. | Methods and compositions for treating systemic lupus erythematosus (sle) with mosunetuzumab |
US20230159633A1 (en) | 2021-11-23 | 2023-05-25 | Janssen Biotech, Inc. | Method of Treating Ulcerative Colitis with Anti-IL23 Specific Antibody |
TW202340251A (en) | 2022-01-19 | 2023-10-16 | 美商建南德克公司 | Anti-notch2 antibodies and conjugates and methods of use |
WO2023141576A1 (en) | 2022-01-21 | 2023-07-27 | Poseida Therapeutics, Inc. | Compositions and methods for delivery of nucleic acids |
WO2023147399A1 (en) | 2022-01-27 | 2023-08-03 | The Rockefeller University | Broadly neutralizing anti-sars-cov-2 antibodies targeting the n-terminal domain of the spike protein and methods of use thereof |
WO2023154824A1 (en) | 2022-02-10 | 2023-08-17 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Human monoclonal antibodies that broadly target coronaviruses |
TW202348252A (en) | 2022-02-16 | 2023-12-16 | 英商梅迪繆思有限公司 | Combination therapies for treatment of cancer with therapeutic binding molecules |
WO2023169896A1 (en) | 2022-03-09 | 2023-09-14 | Astrazeneca Ab | BINDING MOLECULES AGAINST FRα |
WO2023170216A1 (en) | 2022-03-11 | 2023-09-14 | Astrazeneca Ab | A SCORING METHOD FOR AN ANTI-FRα ANTIBODY-DRUG CONJUGATE THERAPY |
WO2023175614A1 (en) | 2022-03-15 | 2023-09-21 | Yeda Research And Development Co. Ltd. | Anti glucocorticoid-induced tnfr-related (gitr) protein antibodies and uses thereof |
TW202346365A (en) | 2022-03-23 | 2023-12-01 | 瑞士商赫孚孟拉羅股份公司 | Combination treatment of an anti-cd20/anti-cd3 bispecific antibody and chemotherapy |
WO2023180511A1 (en) | 2022-03-25 | 2023-09-28 | F. Hoffmann-La Roche Ag | Improved chimeric receptors |
US20230312703A1 (en) | 2022-03-30 | 2023-10-05 | Janssen Biotech, Inc. | Method of Treating Psoriasis with IL-23 Specific Antibody |
WO2023192436A1 (en) | 2022-03-31 | 2023-10-05 | Alexion Pharmaceuticals, Inc. | Singleplex or multiplexed assay for complement markers in fresh biological samples |
WO2023192478A1 (en) | 2022-04-01 | 2023-10-05 | Bristol-Myers Squibb Company | Combination therapy with anti-il-8 antibodies and anti-pd-1 antibodies for treating cancer |
US20230416361A1 (en) | 2022-04-06 | 2023-12-28 | Mirobio Limited | Engineered cd200r antibodies and uses thereof |
GB202205203D0 (en) | 2022-04-08 | 2022-05-25 | UCB Biopharma SRL | Combination with inhibitor |
GB202205200D0 (en) | 2022-04-08 | 2022-05-25 | Ucb Biopharma Sprl | Combination with chemotherapy |
WO2023198727A1 (en) | 2022-04-13 | 2023-10-19 | F. Hoffmann-La Roche Ag | Pharmaceutical compositions of anti-cd20/anti-cd3 bispecific antibodies and methods of use |
WO2023209177A1 (en) | 2022-04-29 | 2023-11-02 | Astrazeneca Uk Limited | Sars-cov-2 antibodies and methods of using the same |
WO2023215737A1 (en) | 2022-05-03 | 2023-11-09 | Genentech, Inc. | Anti-ly6e antibodies, immunoconjugates, and uses thereof |
US20230374122A1 (en) | 2022-05-18 | 2023-11-23 | Janssen Biotech, Inc. | Method for Evaluating and Treating Psoriatic Arthritis with IL23 Antibody |
WO2023235699A1 (en) | 2022-05-31 | 2023-12-07 | Jounce Therapeutics, Inc. | Antibodies to lilrb4 and uses thereof |
WO2023240124A1 (en) | 2022-06-07 | 2023-12-14 | Regeneron Pharmaceuticals, Inc. | Pseudotyped viral particles for targeting tcr-expressing cells |
WO2023240058A2 (en) | 2022-06-07 | 2023-12-14 | Genentech, Inc. | Prognostic and therapeutic methods for cancer |
WO2023250402A2 (en) | 2022-06-22 | 2023-12-28 | Antlera Therapeutics Inc. | Tetravalent fzd and wnt co-receptor binding antibody molecules and uses thereof |
WO2024015953A1 (en) | 2022-07-15 | 2024-01-18 | Danisco Us Inc. | Methods for producing monoclonal antibodies |
WO2024020407A1 (en) | 2022-07-19 | 2024-01-25 | Staidson Biopharma Inc. | Antibodies specifically recognizing b- and t-lymphocyte attenuator (btla) and uses thereof |
WO2024020564A1 (en) | 2022-07-22 | 2024-01-25 | Genentech, Inc. | Anti-steap1 antigen-binding molecules and uses thereof |
WO2024026472A2 (en) | 2022-07-29 | 2024-02-01 | Alector Llc | Transferrin receptor antigen-binding domains and uses therefor |
WO2024026447A1 (en) | 2022-07-29 | 2024-02-01 | Alector Llc | Anti-gpnmb antibodies and methods of use thereof |
WO2024026471A1 (en) | 2022-07-29 | 2024-02-01 | Alector Llc | Cd98hc antigen-binding domains and uses therefor |
WO2024030829A1 (en) | 2022-08-01 | 2024-02-08 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Monoclonal antibodies that bind to the underside of influenza viral neuraminidase |
WO2024050354A1 (en) | 2022-08-31 | 2024-03-07 | Washington University | Alphavirus antigen binding antibodies and uses thereof |
WO2024050524A1 (en) | 2022-09-01 | 2024-03-07 | University Of Georgia Research Foundation, Inc. | Compositions and methods for directing apolipoprotein l1 to induce mammalian cell death |
WO2024049949A1 (en) | 2022-09-01 | 2024-03-07 | Genentech, Inc. | Therapeutic and diagnostic methods for bladder cancer |
WO2024050526A1 (en) | 2022-09-02 | 2024-03-07 | Biomarin Pharmaceutical Inc. | Compositions and methods for treating long qt syndrome |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1990002809A1 (en) * | 1988-09-02 | 1990-03-22 | Protein Engineering Corporation | Generation and selection of recombinant varied binding proteins |
WO1990004788A1 (en) * | 1988-10-28 | 1990-05-03 | Genentech, Inc. | Method for identifying active domains and amino acid residues in polypeptides and hormone variants |
Family Cites Families (45)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3853832A (en) * | 1971-04-27 | 1974-12-10 | Harmone Res Foundation | Synthetic human pituitary growth hormone and method of producing it |
US3853833A (en) * | 1971-04-27 | 1974-12-10 | Hormone Res Foundation | Synthetic human growth-promoting and lactogenic hormones and method of producing same |
US4880910A (en) * | 1981-09-18 | 1989-11-14 | Genentech, Inc. | Terminal methionyl bovine growth hormone and its use |
US4593002A (en) * | 1982-01-11 | 1986-06-03 | Salk Institute Biotechnology/Industrial Associates, Inc. | Viruses with recombinant surface proteins |
US4446235A (en) * | 1982-03-22 | 1984-05-01 | Genentech, Inc. | Method for cloning human growth hormone varient genes |
US4670393A (en) * | 1982-03-22 | 1987-06-02 | Genentech, Inc. | DNA vectors encoding a novel human growth hormone-variant protein |
US4673641A (en) * | 1982-12-16 | 1987-06-16 | Molecular Genetics Research And Development Limited Partnership | Co-aggregate purification of proteins |
US4699897A (en) * | 1983-06-04 | 1987-10-13 | Amgen | Biologically active peptides structurally related to regions within growth hormones |
US4888286A (en) * | 1984-02-06 | 1989-12-19 | Creative Biomolecules, Inc. | Production of gene and protein analogs through synthetic gene design using double stranded synthetic oligonucleotides |
US4655160A (en) * | 1985-09-10 | 1987-04-07 | David R. Ligh | Deck box |
US5013653A (en) * | 1987-03-20 | 1991-05-07 | Creative Biomolecules, Inc. | Product and process for introduction of a hinge region into a fusion protein to facilitate cleavage |
IT1223577B (en) * | 1987-12-22 | 1990-09-19 | Eniricerche Spa | IMPROVED PROCEDURE FOR THE PREPARATION OF THE NATURAL HUMAN GROWTH HORMONE IN PURE FORM |
US5223409A (en) * | 1988-09-02 | 1993-06-29 | Protein Engineering Corp. | Directed evolution of novel binding proteins |
US5663143A (en) * | 1988-09-02 | 1997-09-02 | Dyax Corp. | Engineered human-derived kunitz domains that inhibit human neutrophil elastase |
US5688666A (en) * | 1988-10-28 | 1997-11-18 | Genentech, Inc. | Growth hormone variants with altered binding properties |
US5534617A (en) * | 1988-10-28 | 1996-07-09 | Genentech, Inc. | Human growth hormone variants having greater affinity for human growth hormone receptor at site 1 |
US5350836A (en) * | 1989-10-12 | 1994-09-27 | Ohio University | Growth hormone antagonists |
US5747334A (en) * | 1990-02-15 | 1998-05-05 | The University Of North Carolina At Chapel Hill | Random peptide library |
US5498538A (en) * | 1990-02-15 | 1996-03-12 | The University Of North Carolina At Chapel Hill | Totally synthetic affinity reagents |
US5427908A (en) * | 1990-05-01 | 1995-06-27 | Affymax Technologies N.V. | Recombinant library screening methods |
US5723286A (en) * | 1990-06-20 | 1998-03-03 | Affymax Technologies N.V. | Peptide library and screening systems |
GB9015198D0 (en) * | 1990-07-10 | 1990-08-29 | Brien Caroline J O | Binding substance |
US5770434A (en) * | 1990-09-28 | 1998-06-23 | Ixsys Incorporated | Soluble peptides having constrained, secondary conformation in solution and method of making same |
US5780279A (en) * | 1990-12-03 | 1998-07-14 | Genentech, Inc. | Method of selection of proteolytic cleavage sites by directed evolution and phagemid display |
ATE164395T1 (en) * | 1990-12-03 | 1998-04-15 | Genentech Inc | METHOD FOR ENRICHMENT OF PROTEIN VARIANTS WITH MODIFIED BINDING PROPERTIES |
US5955341A (en) * | 1991-04-10 | 1999-09-21 | The Scripps Research Institute | Heterodimeric receptor libraries using phagemids |
CA2108147C (en) * | 1991-04-10 | 2009-01-06 | Angray Kang | Heterodimeric receptor libraries using phagemids |
US5733743A (en) * | 1992-03-24 | 1998-03-31 | Cambridge Antibody Technology Limited | Methods for producing members of specific binding pairs |
ES2168277T3 (en) * | 1992-09-04 | 2002-06-16 | Scripps Research Inst | PHAGEMIDS THAT CO-EXPRESS A SURFACE RECEIVER AND A SURFACE HETEROLOGY PROTEIN. |
CA2115811A1 (en) * | 1993-02-17 | 1994-08-18 | Claus Krebber | A method for in vivo selection of ligand-binding proteins |
SE9304060D0 (en) * | 1993-12-06 | 1993-12-06 | Bioinvent Int Ab | Methods to select specific bacteriophages |
US5811093A (en) * | 1994-04-05 | 1998-09-22 | Exponential Biotherapies, Inc. | Bacteriophage genotypically modified to delay inactivations by the host defense system |
EP0760012A4 (en) * | 1994-06-10 | 1997-07-02 | Symbiotech Inc | Method of detecting compounds utilizing genetically modified lambdoid bacteriophage |
US5516637A (en) * | 1994-06-10 | 1996-05-14 | Dade International Inc. | Method involving display of protein binding pairs on the surface of bacterial pili and bacteriophage |
US5627024A (en) * | 1994-08-05 | 1997-05-06 | The Scripps Research Institute | Lambdoid bacteriophage vectors for expression and display of foreign proteins |
GB9500851D0 (en) * | 1995-01-17 | 1995-03-08 | Bionvent International Ab | Method of selecting specific bacteriophages |
US5702892A (en) * | 1995-05-09 | 1997-12-30 | The United States Of America As Represented By The Department Of Health And Human Services | Phage-display of immunoglobulin heavy chain libraries |
EP0854933B1 (en) * | 1995-09-07 | 2003-05-07 | Novozymes A/S | Phage display for detergent enzyme activity |
US5622699A (en) * | 1995-09-11 | 1997-04-22 | La Jolla Cancer Research Foundation | Method of identifying molecules that home to a selected organ in vivo |
EP0904541B1 (en) * | 1996-03-20 | 2004-10-06 | Dyax Corp. | PURIFICATION OF TISSUE PLASMINOGEN ACTIVATOR (tPA) |
WO1997044491A1 (en) * | 1996-05-22 | 1997-11-27 | The Johns Hopkins University | Methods of detection utilizing modified bacteriophage |
AU734638B2 (en) * | 1996-06-06 | 2001-06-21 | Lajolla Pharmaceutical Company | aPL immunoreactive peptides, conjugates thereof and methods of treatment for aPL antibody-mediated pathologies |
DE69731226T2 (en) * | 1996-06-10 | 2006-03-09 | The Scripps Research Institute, La Jolla | USE OF SUBSTRATE SUBTRACTION LIBRARIES FOR THE DISTINCTION OF ENZYME SPECIFICATIONS |
WO1998005344A1 (en) * | 1996-08-05 | 1998-02-12 | Brigham And Women's Hospital, Inc. | Bacteriophage-mediated gene therapy |
ATE230850T1 (en) * | 1996-10-08 | 2003-01-15 | Bisys B V U | METHOD AND MEANS FOR SELECTING PEPTIDES AND PROTEINS WITH SPECIFIC AFFINITY FOR A TARGET MOLECULE |
-
1991
- 1991-12-03 AT AT92902109T patent/ATE164395T1/en not_active IP Right Cessation
- 1991-12-03 US US08/050,058 patent/US5750373A/en not_active Expired - Lifetime
- 1991-12-03 CA CA002405246A patent/CA2405246A1/en not_active Abandoned
- 1991-12-03 DE DE69129154T patent/DE69129154T2/en not_active Expired - Lifetime
- 1991-12-03 EP EP92902109A patent/EP0564531B1/en not_active Expired - Lifetime
- 1991-12-03 DK DK92902109T patent/DK0564531T3/en active
- 1991-12-03 ES ES92902109T patent/ES2113940T3/en not_active Expired - Lifetime
- 1991-12-03 CA CA002095633A patent/CA2095633C/en not_active Expired - Lifetime
- 1991-12-03 WO PCT/US1991/009133 patent/WO1992009690A2/en active IP Right Grant
-
1995
- 1995-06-05 US US08/463,587 patent/US5821047A/en not_active Expired - Lifetime
- 1995-06-05 US US08/463,667 patent/US5834598A/en not_active Expired - Lifetime
-
1997
- 1997-09-03 US US08/923,854 patent/US6040136A/en not_active Expired - Fee Related
-
1998
- 1998-03-27 GR GR980400652T patent/GR3026468T3/en unknown
-
2005
- 2005-08-08 US US11/199,062 patent/US20060115874A1/en not_active Abandoned
-
2007
- 2007-06-11 US US11/761,180 patent/US20080038717A1/en not_active Abandoned
-
2009
- 2009-07-24 US US12/508,859 patent/US20100035236A1/en not_active Abandoned
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1990002809A1 (en) * | 1988-09-02 | 1990-03-22 | Protein Engineering Corporation | Generation and selection of recombinant varied binding proteins |
WO1990004788A1 (en) * | 1988-10-28 | 1990-05-03 | Genentech, Inc. | Method for identifying active domains and amino acid residues in polypeptides and hormone variants |
Non-Patent Citations (2)
Title |
---|
Protein Engineering, editors D.L. Oxender et al.; Alan R. Liss Inc., 1987, (New York, US) W.J. Rutter et al.: "Redesigning proteins via genetic engineering", pages 257-267, see the whole article * |
Science, volume 247, 23 March 1990; B.C. Cunningham et al.: "Engineering human prolactin to bind to the human growth hormone receptor", pages 1461-1465, see the whole article (cited in the application) * |
Cited By (1264)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5854026A (en) * | 1988-10-28 | 1998-12-29 | Genentech, Inc. | Human growth hormone variant having enhanced affinity for human growth hormone receptor at site 1 |
US6022711A (en) * | 1988-10-28 | 2000-02-08 | Genentech, Inc. | Human growth hormone variants having enhanced affinity for human growth hormone receptor at site 1 |
US6143523A (en) * | 1988-10-28 | 2000-11-07 | Genentech, Inc. | Human growth hormone variants |
US5534617A (en) * | 1988-10-28 | 1996-07-09 | Genentech, Inc. | Human growth hormone variants having greater affinity for human growth hormone receptor at site 1 |
US5688666A (en) * | 1988-10-28 | 1997-11-18 | Genentech, Inc. | Growth hormone variants with altered binding properties |
US5681809A (en) * | 1989-10-12 | 1997-10-28 | Ohio University | Growth hormone antagonists |
US7553617B1 (en) | 1990-06-20 | 2009-06-30 | Affymax, Inc. | Peptide library and screening systems |
US5723286A (en) * | 1990-06-20 | 1998-03-03 | Affymax Technologies N.V. | Peptide library and screening systems |
US5432018A (en) * | 1990-06-20 | 1995-07-11 | Affymax Technologies N.V. | Peptide library and screening systems |
US7732377B2 (en) | 1990-07-10 | 2010-06-08 | Medical Research Council | Methods for producing members of specific binding pairs |
US6806079B1 (en) | 1990-07-10 | 2004-10-19 | Medical Research Council | Methods for producing members of specific binding pairs |
US7723270B1 (en) | 1990-07-10 | 2010-05-25 | Medical Research Council | Methods for producing members of specific binding pairs |
US7662557B2 (en) | 1990-07-10 | 2010-02-16 | Medical Research Council | Methods for producing members of specific binding pairs |
US7635666B1 (en) | 1990-07-10 | 2009-12-22 | Medical Research Council | Methods for producing members of specific binding pairs |
US5969108A (en) * | 1990-07-10 | 1999-10-19 | Medical Research Council | Methods for producing members of specific binding pairs |
US7063943B1 (en) | 1990-07-10 | 2006-06-20 | Cambridge Antibody Technology | Methods for producing members of specific binding pairs |
US6916605B1 (en) | 1990-07-10 | 2005-07-12 | Medical Research Council | Methods for producing members of specific binding pairs |
US6936440B1 (en) | 1991-05-10 | 2005-08-30 | Genentech, Inc. | Selecting ligand agonists and antagonists |
US6800740B1 (en) | 1991-05-10 | 2004-10-05 | Genentech, Inc. | Variants of native growth hormones having non naturally occurring amino acid sequences or covalent modifications |
US5871907A (en) * | 1991-05-15 | 1999-02-16 | Medical Research Council | Methods for producing members of specific binding pairs |
US6291650B1 (en) | 1991-05-15 | 2001-09-18 | Cambridge Antibody Technology, Ltd. | Methods for producing members of specific binding pairs |
US6492160B1 (en) | 1991-05-15 | 2002-12-10 | Cambridge Antibody Technology Limited | Methods for producing members of specific binding pairs |
US6225447B1 (en) | 1991-05-15 | 2001-05-01 | Cambridge Antibody Technology Ltd. | Methods for producing members of specific binding pairs |
US6730483B2 (en) | 1991-07-08 | 2004-05-04 | Deutsches Krebsforschungszentrum Stiftung Des Offentlichen Rechts | Phagemid for antibody screening |
US5985588A (en) * | 1991-07-08 | 1999-11-16 | Deutsches Krebsforschungszentrum Stiftung Des Offentlichen Rechts | Phagemid for antibody screening |
US6387627B1 (en) | 1991-07-08 | 2002-05-14 | Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts | Phagemid for antibody screening |
WO1993001288A1 (en) * | 1991-07-08 | 1993-01-21 | Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts | Phagemide for screening antibodies |
EP1065271A1 (en) * | 1991-07-08 | 2001-01-03 | Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts | Phagemide for screening antibodies |
US5849500A (en) * | 1991-07-08 | 1998-12-15 | Deutsches Krebsforschungszentrum Stiftung Des Offentlichen Rechts | Phagemid for antibody screening |
US6127132A (en) * | 1991-07-08 | 2000-10-03 | Deutsches Krebsforschungszentrum Stiftung Des Offentlichen Rechts | Phagemid library for antibody screening |
US6172197B1 (en) | 1991-07-10 | 2001-01-09 | Medical Research Council | Methods for producing members of specific binding pairs |
US5733731A (en) * | 1991-10-16 | 1998-03-31 | Affymax Technologies N.V. | Peptide library and screening method |
US6156511A (en) * | 1991-10-16 | 2000-12-05 | Affymax Technologies N.V. | Peptide library and screening method |
US5498530A (en) * | 1991-10-16 | 1996-03-12 | Affymax Technologies, N.V. | Peptide library and screening method |
US6544731B1 (en) | 1991-12-02 | 2003-04-08 | Medical Research Council | Production of anti-self antibodies from antibody segment repertories and displayed on phage |
US7195866B2 (en) | 1991-12-02 | 2007-03-27 | Medical Research Council | Production of anti-self antibodies from antibody segment repertoires and displayed on phage |
US6521404B1 (en) | 1991-12-02 | 2003-02-18 | Medical Research Council | Production of anti-self antibodies from antibody segment repertoires and displayed on phage |
US6555313B1 (en) | 1991-12-02 | 2003-04-29 | Medical Research Council | Production of anti-self antibodies from antibody segment repertoires and displayed on phage |
US6582915B1 (en) | 1991-12-02 | 2003-06-24 | Medical Research Council | Production of anti-self bodies from antibody segment repertories and displayed on phage |
US6593081B1 (en) | 1991-12-02 | 2003-07-15 | Medical Research Council | Production of anti-self antibodies from antibody segment repertoires and displayed on phage |
US5885793A (en) * | 1991-12-02 | 1999-03-23 | Medical Research Council | Production of anti-self antibodies from antibody segment repertoires and displayed on phage |
US6140471A (en) * | 1992-03-24 | 2000-10-31 | Cambridge Antibody Technology, Ltd. | Methods for producing members of specific binding pairs |
US5733743A (en) * | 1992-03-24 | 1998-03-31 | Cambridge Antibody Technology Limited | Methods for producing members of specific binding pairs |
US5962255A (en) * | 1992-03-24 | 1999-10-05 | Cambridge Antibody Technology Limited | Methods for producing recombinant vectors |
US5858657A (en) * | 1992-05-15 | 1999-01-12 | Medical Research Council | Methods for producing members of specific binding pairs |
US6136563A (en) * | 1993-05-25 | 2000-10-24 | Genentech, Inc. | Human growth hormone variants comprising amino acid substitutions |
US6004931A (en) * | 1993-05-25 | 1999-12-21 | Genentech, Inc. | Method for inhibiting growth hormone action |
US5763575A (en) * | 1993-07-26 | 1998-06-09 | Cor Therapeutics, Inc. | Agonist and antagonist peptides of the C140 receptor |
US7834143B2 (en) | 1993-07-26 | 2010-11-16 | Johan Sundelin | Recombinant C140 receptor, its agonists and antagonists, and nucleic acids encoding the receptor |
US7351792B2 (en) | 1993-07-26 | 2008-04-01 | Millennium Pharmaceuticals, Inc. | Recombinant C140 receptor, its agonists and antagonists, and nucleic acids encoding the receptor |
WO1995018856A1 (en) | 1993-12-30 | 1995-07-13 | President And Fellows Of Harvard College | Vertebrate embryonic pattern-inducing hedgehog-like proteins |
EP1958966A2 (en) | 1994-07-01 | 2008-08-20 | Dana-Farber Cancer Institute | Methods for modulating T cell responses by manipulating a common cytokine receptor gamma chain |
US6335319B1 (en) * | 1994-11-15 | 2002-01-01 | Metabolic Pharmaceuticals, Inc. | Treatment of obesity |
EP1568772A3 (en) * | 1995-09-21 | 2006-05-17 | Genentech, Inc. | Human growth hormone variants |
EP1568771A3 (en) * | 1995-09-21 | 2006-05-17 | Genentech, Inc. | Human growth hormone variants |
EP1568771A2 (en) * | 1995-09-21 | 2005-08-31 | Genentech, Inc. | Human growth hormone variants |
EP1568772A2 (en) * | 1995-09-21 | 2005-08-31 | Genentech, Inc. | Human growth hormone variants |
US6057292A (en) * | 1995-09-21 | 2000-05-02 | Genentech, Inc. | Method for inhibiting growth hormone action |
US5849535A (en) * | 1995-09-21 | 1998-12-15 | Genentech, Inc. | Human growth hormone variants |
AU718439B2 (en) * | 1995-09-21 | 2000-04-13 | Genentech Inc. | Human growth hormone variants |
WO1997011178A1 (en) * | 1995-09-21 | 1997-03-27 | Genentech, Inc. | Human growth hormone variants |
US7368111B2 (en) | 1995-10-06 | 2008-05-06 | Cambridge Antibody Technology Limited | Human antibodies specific for TGFβ2 |
WO1997017613A1 (en) * | 1995-11-10 | 1997-05-15 | Elan Corporation, Plc | Peptides which enhance transport across tissues and methods of identifying and using the same |
EP1281718A2 (en) * | 1995-11-10 | 2003-02-05 | ELAN CORPORATION, Plc | Peptides which enhance transport across tissues |
EP1281718A3 (en) * | 1995-11-10 | 2005-01-19 | ELAN CORPORATION, Plc | Peptides which enhance transport across tissues |
WO1997017614A1 (en) * | 1995-11-10 | 1997-05-15 | Elan Corporation, Plc | Peptides which enhance transport across tissues and methods of identifying and using the same |
EP2305713A1 (en) | 1996-02-09 | 2011-04-06 | Abbott Biotechnology Ltd | Human antibodies that bind human TNFalpha |
EP2397494A1 (en) | 1996-02-09 | 2011-12-21 | Abbott Biotechnology Ltd | Human antibodies that bind human TNFalpha |
EP2305712A1 (en) | 1996-02-09 | 2011-04-06 | Abbott Biotechnology Ltd | Human antibodies that bind human TNFalpha |
EP2357200A1 (en) | 1996-02-09 | 2011-08-17 | Abbott Biotechnology Ltd | Human antibodies that bind human TNFalpha |
EP2930186A1 (en) | 1996-02-09 | 2015-10-14 | AbbVie Biotechnology Ltd | Human antibodies that bind human tnfalpha |
EP2930187A1 (en) | 1996-02-09 | 2015-10-14 | AbbVie Biotechnology Ltd | Human antibodies that bind human tnfalpha |
EP2930185A1 (en) | 1996-02-09 | 2015-10-14 | AbbVie Biotechnology Ltd | Human antibodies that bind human tnfalpha |
EP2933267A1 (en) | 1996-02-09 | 2015-10-21 | AbbVie Biotechnology Ltd | Human antibodies that bind human tnfalpha |
WO1997035194A3 (en) * | 1996-03-21 | 1997-12-18 | Enantiomeric screening process, and compositions therefor | |
WO1997035194A2 (en) * | 1996-03-21 | 1997-09-25 | President And Fellows Of Harvard College | Enantiomeric screening process, and compositions therefor |
US8362084B2 (en) | 1996-03-26 | 2013-01-29 | President And Fellows Of Harvard College | Histone deacetylases, and uses related thereto |
US8426592B2 (en) | 1996-03-26 | 2013-04-23 | President And Fellows Of Harvard College | Histone deacetylases, and uses related thereto |
US8399233B2 (en) | 1996-03-26 | 2013-03-19 | President And Fellows Of Harvard College | Histone deacetylases, and uses related thereto |
US8329945B2 (en) | 1996-03-26 | 2012-12-11 | President And Fellows Of Harvard College | Histone deacetylases, and uses related thereto |
US8329946B2 (en) | 1996-03-26 | 2012-12-11 | President And Fellows Of Harvard College | Histone deacetylases, and uses related thereto |
US7566766B2 (en) | 1996-11-08 | 2009-07-28 | EUSA Pharma Ltd. | Peptides which enhance transport across tissues and methods of identifying and using the same |
US6361938B1 (en) | 1996-11-08 | 2002-03-26 | Elan Corporation, Plc | Peptides which enhance transport across tissues and methods of identifying and using the same |
US6497874B1 (en) | 1997-02-05 | 2002-12-24 | Maardh Sven | Recombinant phages |
EP2298899A2 (en) | 1997-04-16 | 2011-03-23 | Millennium Pharmaceuticals, Inc. | CRSP proteins (cysteine-rich secreted proteins), nucleic acid molecules encoding them and uses therefor |
US6770624B2 (en) | 1997-06-04 | 2004-08-03 | The Regents Of The University Of California | Treatment of heart failure with growth hormone |
US6306826B1 (en) | 1997-06-04 | 2001-10-23 | The Regents Of The University Of California | Treatment of heart failure with growth hormone |
US8563687B2 (en) | 1997-07-21 | 2013-10-22 | Ohio University | Synthetic genes for plant gums and other hydroxyproline rich glycoproteins |
US7378506B2 (en) | 1997-07-21 | 2008-05-27 | Ohio University | Synthetic genes for plant gums and other hydroxyproline-rich glycoproteins |
US8871468B2 (en) | 1997-07-21 | 2014-10-28 | Ohio University | Synthetic genes for plant gums and other hydroxyproline-rich glycoproteins |
US6667150B1 (en) | 1997-08-01 | 2003-12-23 | Morphosys Ag | Method and phage for the identification of nucleic acid sequences encoding members of a multimeric (poly) peptide complex |
US7049135B2 (en) | 1997-08-01 | 2006-05-23 | Morphosys Ag | Method and phage for the identification of nucleic acid sequences encoding members of a multimeric (poly)peptide complex |
GB2375765B (en) * | 1997-11-14 | 2003-02-26 | Kymed Gb Ltd | Tagged growth hormone molecules |
GB2375765A (en) * | 1997-11-14 | 2002-11-27 | Kymed Gb Ltd | Tagged growth hormone molecules |
US6680207B1 (en) | 1997-11-14 | 2004-01-20 | Generic Biologicals Limited | Detection of molecules in samples |
WO1999026069A1 (en) * | 1997-11-14 | 1999-05-27 | Generic Biologicals Limited | Improvements in or relating to detection of molecules in samples |
US7056517B2 (en) | 1998-04-13 | 2006-06-06 | The Forsyth Institute | Glucosyltransferase immunogens |
US7163682B2 (en) | 1998-04-13 | 2007-01-16 | The Forsyth Institute | Glucan binding protein and glucosyltransferase immunogens |
WO2000006717A3 (en) * | 1998-07-27 | 2000-06-29 | Genentech Inc | Improved transformation efficiency in phage display through modification of a coat protein |
WO2000006717A2 (en) * | 1998-07-27 | 2000-02-10 | Genentech, Inc. | Improved transformation efficiency in phage display through modification of a coat protein |
US8685893B2 (en) | 1998-07-27 | 2014-04-01 | Genentech, Inc. | Phage display |
WO2000018933A1 (en) * | 1998-09-30 | 2000-04-06 | American Foundation For Biological Research, Inc. | Immunotherapy of cancer through expression of truncated tumor or tumor-associated antigen |
US6387888B1 (en) | 1998-09-30 | 2002-05-14 | American Foundation For Biological Research, Inc. | Immunotherapy of cancer through expression of truncated tumor or tumor-associated antigen |
US6485972B1 (en) | 1998-10-15 | 2002-11-26 | President And Fellows Of Harvard College | WNT signalling in reproductive organs |
US6420110B1 (en) | 1998-10-19 | 2002-07-16 | Gpc Biotech, Inc. | Methods and reagents for isolating biologically active peptides |
EP2301947A2 (en) | 1999-02-26 | 2011-03-30 | Millennium Pharmaceuticals, Inc. | Secreted proteins and uses thereof |
US6616926B1 (en) | 1999-03-03 | 2003-09-09 | Curis, Inc. | Methods of modulating lipid metabolism and storage |
EP2301970A1 (en) | 1999-03-25 | 2011-03-30 | Abbott GmbH & Co. KG | Human antibodies that bind human IL-12 and methods for producing |
EP2168984A1 (en) | 1999-03-25 | 2010-03-31 | Abbott GmbH & Co. KG | Human antibodies that bind human IL-12 and methods for producing |
US8865174B2 (en) | 1999-03-25 | 2014-10-21 | Abbvie Inc. | Methods of treatment using human antibodies that bind IL-12 |
US7504485B2 (en) | 1999-03-25 | 2009-03-17 | Abbott Gmbh & Co., Kg | Human antibodies that bind human IL-12 |
US6914128B1 (en) | 1999-03-25 | 2005-07-05 | Abbott Gmbh & Co. Kg | Human antibodies that bind human IL-12 and methods for producing |
US9035030B2 (en) | 1999-03-25 | 2015-05-19 | AbbVie Deutschland GmbH & Co. KG | Human antibodies that bind the P40 subunit of human IL-12 and methods for using the same |
EP2319870A2 (en) | 1999-03-25 | 2011-05-11 | Abbott GmbH & Co. KG | Human antibodies that bind human IL-12 and methods for producing |
US7883704B2 (en) | 1999-03-25 | 2011-02-08 | Abbott Gmbh & Co. Kg | Methods for inhibiting the activity of the P40 subunit of human IL-12 |
US8765918B2 (en) | 1999-03-25 | 2014-07-01 | Abbott Gmbh & Co., Kg | Human antibodies that bind human interleukin-12 |
US6777194B1 (en) | 1999-04-01 | 2004-08-17 | Dakocytomation Denmark A/S | Monoclonal antibodies against human protein Mcm3, process for their production, and their use |
US7151169B2 (en) | 1999-04-30 | 2006-12-19 | Cambridge Antibody Technology Limited | Specific binding members for TGFβ1 |
US7396905B1 (en) | 1999-05-21 | 2008-07-08 | Mckeon Frank | Calcipressins: endogenous inhibitors of calcineurin, uses and reagents related thereto |
US8137923B2 (en) | 1999-06-30 | 2012-03-20 | Millennium Pharmaceuticals, Inc. | Glycoprotein VI and uses thereof |
US7597888B2 (en) | 1999-06-30 | 2009-10-06 | Millennium Pharmaceuticals, Inc. | Glycoprotein VI and uses thereof |
WO2001000810A1 (en) | 1999-06-30 | 2001-01-04 | Millennium Pharmaceuticals, Inc. | Glycoprotein vi and uses thereof |
US7101549B2 (en) | 1999-06-30 | 2006-09-05 | Millennium Pharmaceuticals, Inc. | Glycoprotein VI and uses thereof |
EP2322558A1 (en) | 1999-06-30 | 2011-05-18 | Millennium Pharmaceuticals, Inc. | Antibodies directed against glycoprotein VI and uses thereof |
EP2902414A1 (en) | 1999-06-30 | 2015-08-05 | Millennium Pharmaceuticals, Inc. | Antibodies directed against glycoprotein VI and uses thereof |
EP1990409A2 (en) | 1999-07-20 | 2008-11-12 | MorphoSys AG | Bacteriophage |
EP2360254A1 (en) | 1999-08-23 | 2011-08-24 | Dana-Farber Cancer Institute, Inc. | Assays for screening anti-pd-1 antibodies and uses thereof |
US8168178B2 (en) | 1999-11-30 | 2012-05-01 | Curis, Inc. | Methods and compositions for regulating lymphocyte activity |
US6951839B1 (en) | 1999-11-30 | 2005-10-04 | Curis, Inc. | Methods and compositions for regulating lymphocyte activity |
EP1626056A2 (en) | 1999-12-30 | 2006-02-15 | President And Fellows of Harvard College | Methods and compositions relating to modulation of hepatocyte growth, plasma cell differentiation or T cell subset activity by modulation of XBP-1 activity |
US7767207B2 (en) | 2000-02-10 | 2010-08-03 | Abbott Laboratories | Antibodies that bind IL-18 and methods of inhibiting IL-18 activity |
EP2338515A2 (en) | 2000-02-10 | 2011-06-29 | Abbott Laboratories | Antibodies that bind human interleukin-18 and methods of making and using |
EP2332579A2 (en) | 2000-02-10 | 2011-06-15 | Abbott Laboratories | Antibodies that bind human interleukin-18 and methods of making and using |
EP2360184A2 (en) | 2000-02-10 | 2011-08-24 | Abbott Laboratories | Antibodies that bind human interleukin-18 and methods of making and using |
WO2001058956A2 (en) | 2000-02-10 | 2001-08-16 | Abbott Laboratories | Antibodies that bind human interleukin-18 and methods of making and using |
US7094539B2 (en) | 2000-03-02 | 2006-08-22 | Promega Corporation | Bacillus stearothermophilus reverse transcription compositions and kits |
US6632645B1 (en) | 2000-03-02 | 2003-10-14 | Promega Corporation | Thermophilic DNA polymerases from Thermoactinomyces vulgaris |
US6436677B1 (en) | 2000-03-02 | 2002-08-20 | Promega Corporation | Method of reverse transcription |
US7504220B2 (en) | 2000-03-02 | 2009-03-17 | Promega Corporation | Method of reverse transcription |
WO2001064954A1 (en) | 2000-03-02 | 2001-09-07 | Promega Corporation | Method of reverse transcription using bacillus steraothermophilus or thermoactinomyces vulgaris dna polymerase |
US7214522B2 (en) | 2000-03-02 | 2007-05-08 | Promega Corporation | Thermophilic DNA polymerases from Thermoactinomyces vulgaris |
US8895284B2 (en) | 2000-03-03 | 2014-11-25 | President And Fellows Of Harvard College | Class II human histone deacetylases, and uses related thereto |
US8435780B2 (en) | 2000-03-03 | 2013-05-07 | President And Fellows Of Harvard College | Class II human histone deacetylases, and uses related thereto |
EP1714661A2 (en) | 2000-05-19 | 2006-10-25 | The Center for Blood Research, INC. | Methods for diagnosing and treating hemostatic disorders by modulating p-selectin activity |
US6573370B1 (en) | 2000-05-19 | 2003-06-03 | Regents Of The University Of Michigan | PON3 and uses thereof |
US6916472B2 (en) | 2000-05-19 | 2005-07-12 | Regents Of The University Of Michigan | PON3 and uses thereof |
EP2251026A1 (en) | 2000-06-08 | 2010-11-17 | Immune Disease Institute, Inc. | Methods and compositions for inhibiting immunoglobulin-mediated reperfusion injury |
WO2002000730A2 (en) | 2000-06-28 | 2002-01-03 | Genetics Institute, Llc. | Pd-l2 molecules: novel pd-1 ligands and uses therefor |
US8475766B2 (en) | 2000-06-29 | 2013-07-02 | Abbvie Inc. | Dual specificity antibodies and methods of making and using |
EP2386575A2 (en) | 2000-06-29 | 2011-11-16 | Abbott Laboratories | Dual specificity antibodies and methods of making and using |
EP2042518A2 (en) | 2000-06-29 | 2009-04-01 | Abbott Laboratories | Dual specificity antibodies and methods of making and using |
US7491516B2 (en) | 2000-06-29 | 2009-02-17 | Abbott Laboratories | Dual specificity antibodies and methods of making and using |
EP2899210A2 (en) | 2000-06-29 | 2015-07-29 | Abbvie Inc. | Dual specificity antibodies and methods of making and using |
WO2002028893A2 (en) | 2000-07-14 | 2002-04-11 | Cropdesign N.V. | Plant cyclin-dependent kinase inhibitors |
US6878861B2 (en) | 2000-07-21 | 2005-04-12 | Washington State University Research Foundation | Acyl coenzyme A thioesterases |
US7405276B2 (en) | 2000-11-01 | 2008-07-29 | Elusys Therapeutics, Inc. | Method of producing bispecific molecules by protein trans-splicing |
EP2316976A1 (en) | 2000-11-28 | 2011-05-04 | Wyeth LLC | Expression analysis of FKBP nucleic acids and polypeptides useful in the diagnosis and treatment of prostate cancer |
EP2295606A1 (en) | 2000-11-28 | 2011-03-16 | Wyeth LLC | Expression analysis of KIAA nucleic acids and polypeptides useful in the diagnosis and treatment of prostate cancer |
US7815907B2 (en) | 2001-01-05 | 2010-10-19 | Amgen Fremont Inc. | Antibodies to insulin-like growth factor I receptor |
EP2796468A2 (en) | 2001-01-05 | 2014-10-29 | Pfizer Inc | Antibodies to insulin-like growth factor I receptor |
US8642037B2 (en) | 2001-01-05 | 2014-02-04 | Amgen Fremont Inc. | Antibodies to insulin-like growth factor I receptor |
US7700742B2 (en) | 2001-01-05 | 2010-04-20 | Amgen Fremont | Antibodies to insulin-like growth factor I receptor |
US9234041B2 (en) | 2001-01-05 | 2016-01-12 | Pfizer Inc. | Antibodies to insulin-like growth factor I receptor |
EP2194067A2 (en) | 2001-01-05 | 2010-06-09 | Pfizer Inc. | Antibodies to insulin-like growth factor I receptor (IGF-IR) |
US7037498B2 (en) | 2001-01-05 | 2006-05-02 | Abgenix, Inc. | Antibodies to insulin-like growth factor I receptor |
US7982024B2 (en) | 2001-01-05 | 2011-07-19 | Amgen Fremont Inc. | Antibodies to insulin-like growth factor I receptor |
EP2292301A2 (en) | 2001-02-22 | 2011-03-09 | Genentech, Inc. | Anti-interferon-alpha antibodies |
EP2065467A2 (en) | 2001-02-22 | 2009-06-03 | Genentech, Inc. | Anti-interferon-alpha antibodies |
EP2077324A2 (en) | 2001-02-23 | 2009-07-08 | DSM IP Assets B.V. | Genes encoding proteolytic enzymes from aspargilli |
EP2123749A2 (en) | 2001-02-23 | 2009-11-25 | DSM IP Assets B.V. | Novel genes encoding novel proteolytic enzymes |
EP1975620A2 (en) | 2001-03-02 | 2008-10-01 | GPC Biotech AG | Three hybrid assay system |
EP2294917A1 (en) | 2001-03-22 | 2011-03-16 | Abbott GmbH & Co. KG | Transgenic animals expressing antibodies specific for genes of interest and uses thereof |
US7795494B2 (en) | 2001-03-22 | 2010-09-14 | Abbott Laboratories | Transgenic mice expressing antibodies specific for genes of interest and uses thereof |
EP2388590A1 (en) | 2001-04-02 | 2011-11-23 | Dana Farber Cancer Institute | PD-1, a receptor for B7-4, and uses thereof |
EP2278013A1 (en) | 2001-04-16 | 2011-01-26 | Wyeth Holdings Corporation | Streptococcus pneumoniae open reading frames encoding polypeptide antigens and uses thereof |
EP2258718A1 (en) | 2001-04-16 | 2010-12-08 | Wyeth Holdings Corporation | Streptococcus pneumoniae open reading frames encoding polypeptide antigens and uses thereof |
EP2258842A1 (en) | 2001-04-16 | 2010-12-08 | Wyeth Holdings Corporation | Streptococcus pneumoniae open reading frames encoding polypeptide antigens and uses thereof |
EP2261241A1 (en) | 2001-04-16 | 2010-12-15 | Wyeth Holdings Corporation | Streptococcus pneumoniae open reading frames encoding polypeptide antigens and uses thereof |
EP2277897A1 (en) | 2001-04-16 | 2011-01-26 | Wyeth Holdings Corporation | Streptococcus pneumoniae open reading frames encoding polypeptide antigens and uses thereof |
US8178579B2 (en) | 2001-05-09 | 2012-05-15 | President And Fellows Of Harvard College | Dioxanes and uses thereof |
EP2940044A1 (en) | 2001-06-08 | 2015-11-04 | AbbVie Biotechnology Ltd | Methods of administering anti-tnfalpha antibodies |
EP2364731A2 (en) | 2001-06-08 | 2011-09-14 | Abbott Biotechnology Ltd | Methods of administering anti-TNFalpha antibodies |
EP3190124A1 (en) | 2001-06-08 | 2017-07-12 | AbbVie Biotechnology Ltd | Adalimumab for use in therapy of rheumatoid arthritis |
WO2002100330A2 (en) | 2001-06-08 | 2002-12-19 | Abbott Biotechnology Ltd | METHODS OF ADMINISTERING ANTI-TNFα ANTIBODIES |
EP2324851A1 (en) | 2001-06-08 | 2011-05-25 | Abbott Biotechnology Ltd | Methods of administering anti-TNFalpha antibodies |
EP2359855A2 (en) | 2001-06-08 | 2011-08-24 | Abbott Biotechnology Ltd | Methods of administering anti-TNFalpha antibodies |
EP2270187A2 (en) | 2001-06-22 | 2011-01-05 | Pioneer Hi-Bred International, Inc. | Defensin polynucleotides and methods of use |
EP2270186A2 (en) | 2001-06-22 | 2011-01-05 | Pioneer Hi-Bred International, Inc. | Defensin polynucleotides and methods of use |
EP2270185A2 (en) | 2001-06-22 | 2011-01-05 | Pioneer Hi-Bred International, Inc. | Defensin polynucleotides and methods of use |
EP2270165A2 (en) | 2001-06-22 | 2011-01-05 | Pioneer Hi-Bred International, Inc. | Defensin polynucleotides and methods of use |
EP2270188A2 (en) | 2001-06-22 | 2011-01-05 | Pioneer Hi-Bred International, Inc. | Defensin polynucleotides and methods of use |
EP2270184A2 (en) | 2001-06-22 | 2011-01-05 | Pioneer Hi-Bred International, Inc. | Defensin polynucleotides and methods of use |
EP2333070A2 (en) | 2001-06-22 | 2011-06-15 | Pioneer Hi-Bred International, Inc. | Defensin polynucleotides and methods of use |
US7745391B2 (en) | 2001-09-14 | 2010-06-29 | Compugen Ltd. | Human thrombospondin polypeptide |
US7288251B2 (en) | 2001-11-09 | 2007-10-30 | Abgenix, Inc. | Antibodies to CD40 |
US7626012B2 (en) | 2001-11-09 | 2009-12-01 | Amgen Fremont Inc. | Nucleic acid molecules which encode antibodies that bind CD40 |
EP2343086A2 (en) | 2001-11-09 | 2011-07-13 | Pfizer Products Inc. | Antibodies to CD40 |
US7618633B2 (en) | 2001-11-09 | 2009-11-17 | Amgen Fremont Inc. | Antibodies that bind CD40 and methods of treating cancer and enhancing immune responses |
WO2003040170A2 (en) | 2001-11-09 | 2003-05-15 | Pfizer Products Inc. | Antibodies to cd40 |
US7338660B2 (en) | 2001-11-09 | 2008-03-04 | Abgenix, Inc. | Methods of treating cancer and enhancing immune responses with antibodies that bind CD40 |
US8388971B2 (en) | 2001-11-09 | 2013-03-05 | Amgen Fremont Inc. | Antibodies that bind CD40 and methods of treating cancer and enhancing immune responses |
US7563442B2 (en) | 2001-11-09 | 2009-07-21 | Abgenix, Inc. | Antibodies to CD40 and methods of treating cancer and enhancing immune responses |
US7572886B2 (en) | 2001-12-18 | 2009-08-11 | Centre National De La Recherche Scientifique | Death associated proteins, and THAP1 and PAR4 pathways in apoptosis control |
US7892727B2 (en) | 2001-12-18 | 2011-02-22 | Centre National De La Recherche Scientifique Cnrs | Chemokine-binding protein and methods of use |
US7858297B2 (en) | 2001-12-18 | 2010-12-28 | Centre National De La Recherche Scientifique Cnrs | Chemokine-binding protein and methods of use |
US7087418B2 (en) | 2001-12-19 | 2006-08-08 | Bristol-Myers Squibb Company | Pichia pastoris formate dehydrogenase and uses therefor |
EP2060628A1 (en) | 2002-02-13 | 2009-05-20 | XOMA Technology Ltd. | Eukaryotic signal sequences for polypeptide expression and polypeptide display libraries |
US7323175B2 (en) | 2002-03-07 | 2008-01-29 | The Forsyth Institute | Immunogenicity of glucan binding protein |
WO2003082914A1 (en) | 2002-04-03 | 2003-10-09 | The University Of Queensland | Prothrombin activating protein |
EP2347766A1 (en) | 2002-04-26 | 2011-07-27 | Abbott Biotechnology Ltd | Use of TNFalpha antibodies and another drug |
EP2196218A2 (en) | 2002-04-26 | 2010-06-16 | Abbott Biotechnology Ltd | Use of anti-TNFalpha antibodies and another drug |
US7588925B2 (en) | 2002-05-21 | 2009-09-15 | Dsm Ip Assets B.V. | Phospholipases and uses thereof |
US7838274B2 (en) | 2002-05-21 | 2010-11-23 | Dsm Ip Assets B.V. | Phospholipases and uses thereof |
US7667099B2 (en) | 2002-06-20 | 2010-02-23 | Board Of Trustees Of Michigan State University | Plastid division and related genes and proteins, and methods of use |
US9303081B2 (en) | 2002-07-18 | 2016-04-05 | Merus B.V. | Recombinant production of mixtures of antibodies |
US7932360B2 (en) | 2002-07-18 | 2011-04-26 | Merus B.V. | Recombinant production of mixtures of antibodies |
US10934571B2 (en) | 2002-07-18 | 2021-03-02 | Merus N.V. | Recombinant production of mixtures of antibodies |
US7927834B2 (en) | 2002-07-18 | 2011-04-19 | Merus B.V. | Recombinant production of mixtures of antibodies |
USRE47770E1 (en) | 2002-07-18 | 2019-12-17 | Merus N.V. | Recombinant production of mixtures of antibodies |
EP2371859A2 (en) | 2002-07-19 | 2011-10-05 | Abbott Biotechnology Ltd | Treatment of TNF alpha related disorders |
EP2336182A1 (en) | 2002-07-19 | 2011-06-22 | Abbott Biotechnology Ltd | Treatment of TNF alpha related disorders |
EP1944322A2 (en) | 2002-07-19 | 2008-07-16 | Abbott Biotechnology Ltd. | Treatment of TNF alpha related disorders |
EP2298810A2 (en) | 2002-07-19 | 2011-03-23 | Abbott Biotechnology Ltd | Treatment of TNF alpha related disorders |
EP2942359A1 (en) | 2002-07-19 | 2015-11-11 | AbbVie Biotechnology Ltd | Treatment of TNF alpha related disorders |
US7250551B2 (en) | 2002-07-24 | 2007-07-31 | President And Fellows Of Harvard College | Transgenic mice expressing inducible human p25 |
US8030456B2 (en) | 2002-08-10 | 2011-10-04 | Yale University | Nogo receptor antagonists |
US7465705B2 (en) | 2002-08-10 | 2008-12-16 | Yale University | Nogo receptor antagonists |
US8216586B2 (en) | 2002-08-19 | 2012-07-10 | Dsm Ip Assets B.V. | Lipases and uses thereof |
EP2338986A1 (en) | 2002-08-19 | 2011-06-29 | DSM IP Assets B.V. | Novel lipases and uses thereof |
US7550280B2 (en) | 2002-08-19 | 2009-06-23 | Dsm Ip Assets B.V. | Lipases and uses thereof |
EP2311979A1 (en) | 2002-08-20 | 2011-04-20 | Millennium Pharmaceuticals, Inc. | Compositions, kits and methods for identification, assessment, prevention and therapy of cervical cancer |
EP2311978A1 (en) | 2002-08-20 | 2011-04-20 | Millennium Pharmaceuticals, Inc. | Compositions, kits, and methods for identification, assessment, prevention, and therapy of cervical cancer |
EP2314716A1 (en) | 2002-08-20 | 2011-04-27 | Millennium Pharmaceuticals, Inc. | Compositions, kits, and methods for identification, assessment, prevention, and therapy of cervical cancer |
EP2305836A1 (en) | 2002-08-20 | 2011-04-06 | Millennium Pharmaceuticals, Inc. | Compositions, kits and methods for identification, assessment, prevention and therapy of cervical cancer |
US7455989B2 (en) | 2002-08-20 | 2008-11-25 | Yeda Research And Development Co. Ltd. | AKAP84 and its use for visualization of biological structures |
EP2311980A1 (en) | 2002-08-20 | 2011-04-20 | Millennium Pharmaceuticals, Inc. | Compositions, kits, and methods for identification, assessment, prevention, and therapy of cervical cancer |
EP2181711A1 (en) | 2002-09-04 | 2010-05-05 | Biopolymer Engineering, Inc. | Cancer therapy using whole glucan particles and antibodies |
EP2290107A1 (en) | 2003-01-07 | 2011-03-02 | Dyax Corporation | Kunitz domain library |
EP2336160A2 (en) | 2003-01-31 | 2011-06-22 | Abbott GmbH & Co. KG | Amyloid-beta(1-42) oligomers, derivatives thereof, antibodies for the same, method for production and use thereof. |
EP2336159A2 (en) | 2003-01-31 | 2011-06-22 | Abbott GmbH & Co. KG | Amyloid-beta(1-42) oligomers, derivatives thereof, antibodies for the same, method for production and use thereof. |
EP2336161A2 (en) | 2003-01-31 | 2011-06-22 | Abbott GmbH & Co. KG | Amyloid-beta(1-42) oligomers, derivatives thereof, antibodies for the same, method for production and use thereof. |
US10464976B2 (en) | 2003-01-31 | 2019-11-05 | AbbVie Deutschland GmbH & Co. KG | Amyloid β(1-42) oligomers, derivatives thereof and antibodies thereto, methods of preparation thereof and use thereof |
EP1592777A2 (en) * | 2003-02-01 | 2005-11-09 | Tanox, Inc. | A method for generating high affinity antibodies |
EP1592777A4 (en) * | 2003-02-01 | 2008-06-04 | Tanox Inc | A method for generating high affinity antibodies |
EP2316969A1 (en) | 2003-03-13 | 2011-05-04 | Fujirebio America, Inc. | Detection of urinary mesothelin-/megakaryocyte potentiating factor-related peptides for assessment of ovarian cancer |
AU2004232962B2 (en) * | 2003-04-16 | 2012-02-02 | Genentech, Inc. | Compositions and methods relating to STOP-1 |
US7799899B2 (en) | 2003-04-16 | 2010-09-21 | Genentech, Inc. | Compositions and methods relating to STOP-1 |
WO2004094476A3 (en) * | 2003-04-16 | 2005-06-16 | Genentech Inc | Compositions and methods relating to stop-1 |
EP2386318A1 (en) | 2003-05-15 | 2011-11-16 | Iogenetics, Inc. | Targeted biocides |
US9738701B2 (en) | 2003-05-30 | 2017-08-22 | Merus N.V. | Method for selecting a single cell expressing a heterogeneous combination of antibodies |
US10605808B2 (en) | 2003-05-30 | 2020-03-31 | Merus N.V. | Antibody producing non-human animals |
US7919257B2 (en) | 2003-05-30 | 2011-04-05 | Merus Biopharmaceuticals, B.V.I.O. | Method for selecting a single cell expressing a heterogeneous combination of antibodies |
US10670599B2 (en) | 2003-05-30 | 2020-06-02 | Merus N.V. | Method for selecting a single cell expressing a heterogeneous combination of antibodies |
EP2508608A1 (en) | 2003-06-09 | 2012-10-10 | Alnylam Pharmaceuticals Inc. | Method of treating neurodegenerative disease |
US8562985B2 (en) | 2003-08-04 | 2013-10-22 | Amgen Fremont Inc. | Antibodies to c-Met |
US7498420B2 (en) | 2003-08-04 | 2009-03-03 | Amgen Fremont Inc. | Antibodies to c-Met |
US8163280B2 (en) | 2003-08-04 | 2012-04-24 | Amgen Fremont Inc. | Antibodies to c-Met |
US8821869B2 (en) | 2003-08-04 | 2014-09-02 | Amgen Fremont Inc. | Treatment methods using c-Met antibodies |
US7326414B2 (en) | 2003-09-10 | 2008-02-05 | Warner-Lambert Company Llc | Antibodies to M-CSF |
US10280219B2 (en) | 2003-09-10 | 2019-05-07 | Amgen Fremont Inc. | Antibodies to M-CSF |
US9718883B2 (en) | 2003-09-10 | 2017-08-01 | Amgen Fremont Inc. | Antibodies to M-CSF |
EP3170840A1 (en) | 2003-09-10 | 2017-05-24 | Warner-Lambert Company LLC | Antibodies to m-csf |
EP2051077A2 (en) | 2003-10-07 | 2009-04-22 | Millennium Pharmaceuticals, Inc. | Nucleic acid molecules and proteins for the identification, assessment, prevention, and therapy of ovarian cancer |
EP2261667A2 (en) | 2003-10-07 | 2010-12-15 | Millennium Pharmaceuticals, Inc. | Nucleic acid molecules and proteins for the identification, assessment, prevention, and their therapy of ovarian cancer |
EP2441474A1 (en) | 2003-10-17 | 2012-04-18 | Joslin Diabetes Center, Inc. | Methods and compositions for modulating adipocyte function |
EP2460830A2 (en) | 2003-11-12 | 2012-06-06 | Abbott Laboratories | IL-18 binding proteins |
EP2385070A1 (en) | 2003-11-12 | 2011-11-09 | Abbott Laboratories | Il-18 binding proteins |
EP2395020A2 (en) | 2003-11-12 | 2011-12-14 | Abbott Laboratories | IL-18 binding proteins |
EP2460829A2 (en) | 2003-11-12 | 2012-06-06 | Abbott Laboratories | IL-18 binding proteins |
US10259872B2 (en) | 2004-01-09 | 2019-04-16 | Pfizer, Inc. | Antibodies to MAdCAM |
USRE45847E1 (en) | 2004-01-09 | 2016-01-19 | Pfizer Inc. | Antibodies to MAdCAM |
US7932372B2 (en) | 2004-01-09 | 2011-04-26 | Amgen Fremont Inc. | Antibodies to MAdCAM |
EP2177537A2 (en) | 2004-01-09 | 2010-04-21 | Pfizer Inc. | Antibodies to MAdCAM |
US9328169B2 (en) | 2004-01-09 | 2016-05-03 | Pfizer Inc. | Human antibodies that bind human MAdCAM |
EP2133427A1 (en) | 2004-01-14 | 2009-12-16 | Ohio University | Methods of producing peptides/proteins in plants and peptides/proteins produced thereby |
US9006410B2 (en) | 2004-01-14 | 2015-04-14 | Ohio University | Nucleic acid for plant expression of a fusion protein comprising hydroxyproline O-glycosylation glycomodule |
US9012371B2 (en) | 2004-01-20 | 2015-04-21 | Merus B.V. | Mixtures of binding proteins |
US8268756B2 (en) | 2004-01-20 | 2012-09-18 | Merus B.V. | Mixture of binding proteins |
EP2444805A2 (en) | 2004-01-21 | 2012-04-25 | Fujirebio America, Inc. | Detection of mesothelin-/megakaryocyte potentiating factor-related peptides in peritoneal fluid for assessment of the peritoneum and the peritoneal cavity |
EP2368579A1 (en) | 2004-01-21 | 2011-09-28 | Novo Nordisk Health Care AG | Transglutaminase mediated conjugation of peptides |
EP2033662A1 (en) | 2004-01-21 | 2009-03-11 | Novo Nordisk Health Care AG | Transglutaminase mediated conjugation of peptides |
EP2290077A2 (en) | 2004-03-01 | 2011-03-02 | Immune Disease Institute, Inc. | Natural IGM antibodies and inhibitors thereof |
EP2293069A2 (en) | 2004-03-24 | 2011-03-09 | Tripath Imaging, Inc. | Methods and compositions for the detection of cervical disease |
EP2335732A2 (en) | 2004-04-09 | 2011-06-22 | Abbott Biotechnology Ltd | Multiple-variable dose regimen for treating TNF-alpha-related disorders |
EP2338516A2 (en) | 2004-04-09 | 2011-06-29 | Abbott Biotechnology Ltd | Multiple-variable dose regimen for treating TNF-alpha-related disorders |
EP2335731A2 (en) | 2004-04-09 | 2011-06-22 | Abbott Biotechnology Ltd | Multiple-variable dose regimen for treating TNF-alpha-related disorders |
US8623812B2 (en) | 2004-04-19 | 2014-01-07 | Ohio University | Cross-linkable glycoproteins and methods of making the same |
EP2270034A2 (en) | 2004-06-03 | 2011-01-05 | Athlomics Pty Ltd | Agents and methods for diagnosing stress |
EP2527447A1 (en) | 2004-06-03 | 2012-11-28 | Athlomics Pty Ltd | Agents and methods for diagnosing stress |
EP2527446A1 (en) | 2004-06-03 | 2012-11-28 | Athlomics Pty Ltd | Agents and methods for diagnosing stress |
US9017287B2 (en) | 2004-06-23 | 2015-04-28 | Abbvie Biotechnology Ltd | Automatic injection devices |
US7618626B2 (en) | 2004-07-16 | 2009-11-17 | Pfizer Inc | Combination treatment for non-hematologic malignancies |
WO2006014744A2 (en) | 2004-07-23 | 2006-02-09 | University Of Massachusetts | Compounds that inhibit hsp90 protein-protein interactions with iap proteins |
EP2290086A2 (en) | 2004-12-22 | 2011-03-02 | Genentech, Inc. | Methods for producing soluble multi-membrane-spanning proteins |
EP2290088A1 (en) | 2004-12-22 | 2011-03-02 | Genentech, Inc. | Methods for producing soluble multi-menbrane-spanning proteins |
EP2290087A2 (en) | 2004-12-22 | 2011-03-02 | Genentech, Inc. | Methods for producing soluble multi-membrane-spanning proteins |
US9856311B2 (en) | 2005-01-05 | 2018-01-02 | F-Star Biotechnologische Forschungs- Und Entwicklungsges.M.B.H | Synthetic immunoglobulin domains with binding properties engineered in regions of the molecule different from the complementarity determining regions |
US10385118B2 (en) | 2005-01-05 | 2019-08-20 | F-Star Biotechnologische Forschungs- Und Entwicklungsges.M.B.H | Synthetic immunoglobulin domains with binding properties engineered in regions of the molecule different from the complementarity determining regions |
EP2392353A1 (en) | 2005-01-28 | 2011-12-07 | Janssen Alzheimer Immunotherapy | Anti A beta antibody formulation |
US9572854B2 (en) | 2005-03-22 | 2017-02-21 | President And Fellows Of Harvard College | Treatment of protein degradation disorders |
US10172905B1 (en) | 2005-03-22 | 2019-01-08 | President And Fellows Of Harvard College | Treatment of protein degradation disorders |
US8999289B2 (en) | 2005-03-22 | 2015-04-07 | President And Fellows Of Harvard College | Treatment of protein degradation disorders |
EP3312196A1 (en) | 2005-03-23 | 2018-04-25 | Genmab A/S | Antibodies against cd38 for treatment of multiple myeloma |
EP2551282A2 (en) | 2005-03-23 | 2013-01-30 | Genmab A/S | Antibodies against CD38 for treatment of multiple myeloma |
EP3153525A1 (en) | 2005-03-23 | 2017-04-12 | Genmab A/S | Antibodies against cd38 for treatment of multiple myeloma |
EP2567976A2 (en) | 2005-03-23 | 2013-03-13 | Genmab A/S | Antibodies against CD38 for treatment of multiple myeloma |
EP2535355A2 (en) | 2005-03-23 | 2012-12-19 | Genmab A/S | Antibodies against CD38 for treatment of multiple myeloma |
EP2295466A2 (en) | 2005-04-25 | 2011-03-16 | Pfizer Inc. | Antibodies to myostatin |
EP2444419A1 (en) | 2005-04-26 | 2012-04-25 | Pfizer Inc. | P-Cadherin antibodies |
EP2444420A1 (en) | 2005-04-26 | 2012-04-25 | Pfizer Inc. | P-Cadherin antibodies |
EP2444421A1 (en) | 2005-04-26 | 2012-04-25 | Pfizer Inc. | P-Cadherin antibodies |
WO2006116442A2 (en) | 2005-04-27 | 2006-11-02 | Tripath Imaging, Inc. | Monoclonal antibodies and methods for their use in the detection of cervical disease |
EP2332988A2 (en) | 2005-04-27 | 2011-06-15 | Tripath Imaging, Inc. | Monoclonal antibodies and methods for their use in the detection of cervical disease |
EP2500037A2 (en) | 2005-05-16 | 2012-09-19 | Abbott Biotechnology Ltd | Use of TNF alpha inhibitor for treatment of erosive polyarthritis |
EP3263581A1 (en) | 2005-05-17 | 2018-01-03 | University of Connecticut | Compositions and methods for immunomodulation in an organism |
EP2460831A2 (en) | 2005-05-27 | 2012-06-06 | Biogen Idec MA Inc. | Tweak binding antibodies |
EP2460832A2 (en) | 2005-05-27 | 2012-06-06 | Biogen Idec MA Inc. | TWEAK binding antibodies |
EP2388274A1 (en) | 2005-06-17 | 2011-11-23 | Janssen Alzheimer Immunotherapy | Methods of purifying anti A Beta antibodies |
US7700739B2 (en) | 2005-06-30 | 2010-04-20 | Abbott Laboratories | IL-12/p40 binding proteins |
US8629257B2 (en) | 2005-06-30 | 2014-01-14 | Abbvie Inc. | IL-12/p40 binding proteins |
EP2476761A2 (en) | 2005-07-07 | 2012-07-18 | Athlomics Pty Ltd | Polynucleotide marker genes and their expression, for diagnosis of endotoxemia |
EP2216653A1 (en) | 2005-08-02 | 2010-08-11 | XBiotech, Inc | Diagnosis, treatment and prevention of vascular disorders using il-1alpha autoantibodies |
WO2007024715A2 (en) | 2005-08-19 | 2007-03-01 | Abbott Laboratories | Dual variable domain immunoglobin and uses thereof |
EP2500358A2 (en) | 2005-08-19 | 2012-09-19 | Abbott Laboratories | Dual variable domain immunoglobulin and uses thereof |
EP2500356A2 (en) | 2005-08-19 | 2012-09-19 | Abbott Laboratories | Dual variable domain immunoglobulin and uses thereof |
EP2500353A2 (en) | 2005-08-19 | 2012-09-19 | Abbott Laboratories | Dual variable domain immunoglobulin and uses thereof |
US7612181B2 (en) | 2005-08-19 | 2009-11-03 | Abbott Laboratories | Dual variable domain immunoglobulin and uses thereof |
EP2500354A2 (en) | 2005-08-19 | 2012-09-19 | Abbott Laboratories | Dual variable domain immunoglobulin and uses thereof |
EP2500355A2 (en) | 2005-08-19 | 2012-09-19 | Abbott Laboratories | Dual variable domain immunoglobulin and uses thereof |
EP2500359A2 (en) | 2005-08-19 | 2012-09-19 | Abbott Laboratories | Dual variable domain immunoglobulin and uses thereof |
EP2520588A1 (en) | 2005-08-19 | 2012-11-07 | Abbott Laboratories | Dual variable domain immunoglobulin and uses thereof |
EP2500352A1 (en) | 2005-08-19 | 2012-09-19 | Abbott Laboratories | Dual variable domain immunoglobulin and uses thereof |
EP2500357A2 (en) | 2005-08-19 | 2012-09-19 | Abbott Laboratories | Dual variable domain immunoglobulin and uses thereof |
WO2007024705A2 (en) | 2005-08-19 | 2007-03-01 | Abbott Biotechnology Ltd. | Method of treating depression using a tnf-alpha antibody |
EP2495257A2 (en) | 2005-08-19 | 2012-09-05 | Abbott Laboratories | Dual variable domain immunoglobulin and uses thereof |
US8080646B2 (en) | 2005-09-07 | 2011-12-20 | Amgen Fremont, Inc. | Human monoclonal antibodies to activin receptor-like kinase-1 |
EP2447283A2 (en) | 2005-09-07 | 2012-05-02 | Amgen Fremont Inc. | Human monoclonal antibodies to activin receptor-like kinase-1 (ALK-1) |
US9221915B2 (en) | 2005-09-07 | 2015-12-29 | Pfizer Inc. | Human monoclonal antibodies to activin receptor-like kinase-1 |
US7537762B2 (en) | 2005-09-07 | 2009-05-26 | Amgen Fremont, Inc. | Human monoclonal antibodies to activin receptor-like kinase-1 |
EP2960253A1 (en) | 2005-09-07 | 2015-12-30 | Amgen Fremont Inc. | Human monoclonal antibodies to activin receptor-like kinase-1 |
EP3381945A1 (en) | 2005-09-07 | 2018-10-03 | Amgen Fremont Inc. | Human monoclonal antibodies to activin receptor-like kinase-1 |
US8906864B2 (en) | 2005-09-30 | 2014-12-09 | AbbVie Deutschland GmbH & Co. KG | Binding domains of proteins of the repulsive guidance molecule (RGM) protein family and functional fragments thereof, and their use |
EP2862867A2 (en) | 2005-10-25 | 2015-04-22 | The Johns Hopkins University | Methods and compositions for the treatment of Marfan syndrome and associated disorders |
EP2357479A1 (en) | 2005-11-01 | 2011-08-17 | Abbott Biotechnology Ltd | Methods and compositions for diagnosing ankylosing spondylitis using biomarkers |
WO2007089303A2 (en) | 2005-11-01 | 2007-08-09 | Abbott Biotechnology Ltd. | Methods and compositions for diagnosing ankylosing spondylitis using biomarkers |
EP2365334A1 (en) | 2005-11-14 | 2011-09-14 | MetaMol Theranostics, LLC | Peptide sequence that promotes tumor invasion |
US7807790B2 (en) | 2005-11-14 | 2010-10-05 | Metamol Theranostics, Llc | Peptide sequence that promotes tumor invasion |
US8969020B2 (en) | 2005-11-14 | 2015-03-03 | Metamol Theranostics Llc | Peptide sequence that promotes tumor invasion |
EP2410335A1 (en) | 2005-11-30 | 2012-01-25 | Massachusetts Institute of Technology (MIT) | Pathogen detection biosensor |
US10208109B2 (en) | 2005-11-30 | 2019-02-19 | Abbvie Inc. | Monoclonal antibodies against amyloid beta protein and uses thereof |
EP2289909A1 (en) | 2005-11-30 | 2011-03-02 | Abbott Laboratories | Screening method, process for purifying of non-diffusible a-beta oligomers, selective antibodies against said non-diffusible a-beta oligomers and a process for manufacturing of said antibodies |
US10323084B2 (en) | 2005-11-30 | 2019-06-18 | Abbvie Inc. | Monoclonal antibodies against amyloid beta protein and uses thereof |
US10538581B2 (en) | 2005-11-30 | 2020-01-21 | Abbvie Inc. | Anti-Aβ globulomer 4D10 antibodies |
US8957187B2 (en) | 2005-12-02 | 2015-02-17 | Genentech, Inc. | Binding polypeptides and uses thereof |
EP2336170A2 (en) | 2005-12-15 | 2011-06-22 | Industrial Technology Research Institute | Recombinant triplex scaffold-based polypeptides |
EP2325208A1 (en) | 2005-12-15 | 2011-05-25 | Genentech, Inc. | Polyubiquitin antibodies |
EP3309170A1 (en) | 2005-12-15 | 2018-04-18 | Genentech, Inc. | Polyubiquitin antibodies |
US10183986B2 (en) | 2005-12-15 | 2019-01-22 | Industrial Technology Research Institute | Trimeric collagen scaffold antibodies |
EP2338912A2 (en) | 2005-12-15 | 2011-06-29 | Industrial Technology Research Institute | Recombinant triplex scaffold-base polypeptides |
EP2455395A1 (en) | 2005-12-19 | 2012-05-23 | Tripath Imaging, Inc. | MCM6 monoclonal antibodies and methods for their use in the detection of cervical disease |
EP3156418A1 (en) | 2006-01-05 | 2017-04-19 | Genentech, Inc. | Anti-ephb4 antibodies and methods using same |
EP2402373A2 (en) | 2006-01-05 | 2012-01-04 | Genentech, Inc. | Anti-EphB4 Antibodies and Methods Using Same |
EP2363711A1 (en) | 2006-01-27 | 2011-09-07 | Tripath Imaging, Inc. | Methods for identifying patients with an increased likelihood of having ovarian cancer and compositions therefor |
US9228015B2 (en) | 2006-01-27 | 2016-01-05 | Biogen Idec Ma Inc. | Nogo receptor antagonists and methods of increasing neurite outgrowth |
US8669345B2 (en) | 2006-01-27 | 2014-03-11 | Biogen Idec Ma Inc. | Nogo receptor antagonists |
EP2526968A2 (en) | 2006-01-27 | 2012-11-28 | Biogen Idec MA Inc. | Nogo receptor antagonists |
US7846439B2 (en) | 2006-02-01 | 2010-12-07 | Cephalon Australia Pty Ltd | Domain antibody construct |
US8754237B2 (en) | 2006-02-14 | 2014-06-17 | President And Fellows Of Harvard College | Bifunctional histone deacetylase inhibitors |
US8222423B2 (en) | 2006-02-14 | 2012-07-17 | Dana-Farber Cancer Institute, Inc. | Bifunctional histone deacetylase inhibitors |
EP2327423A2 (en) | 2006-02-21 | 2011-06-01 | Wyeth LLC | Human antibodies against human interleukin-22 (IL-22) |
EP3020729A1 (en) | 2006-02-21 | 2016-05-18 | Wyeth LLC | Antibodies against human il-22 and uses therefor |
EP2431392A1 (en) | 2006-02-21 | 2012-03-21 | Wyeth LLC | Antibodies against human IL-22 and uses therefor |
EP2468772A2 (en) | 2006-03-16 | 2012-06-27 | Genentech, Inc. | Antibodies to EGFL7 and methods for their use |
US8278421B2 (en) | 2006-03-20 | 2012-10-02 | Xoma Techolology Ltd. | Human antibodies specific for gastrin materials and methods |
EP3088410A2 (en) | 2006-04-05 | 2016-11-02 | AbbVie Biotechnology Ltd | Antibody purification |
EP2738179A1 (en) | 2006-04-05 | 2014-06-04 | AbbVie Biotechnology Ltd | Antibody purification |
EP2738178A1 (en) | 2006-04-05 | 2014-06-04 | AbbVie Biotechnology Ltd | Antibody purification |
EP2708242A2 (en) | 2006-04-10 | 2014-03-19 | Abbott Biotechnology Ltd | Uses and compositions for treatment of ankylosing spondylitis |
EP2666478A2 (en) | 2006-04-10 | 2013-11-27 | Abbott Biotechnology Ltd | Uses and compositions for treatment of psoriasis |
EP2666480A2 (en) | 2006-04-10 | 2013-11-27 | Abbott Biotechnology Ltd | Uses and compositions for treatment of Crohn's desease |
EP2703010A2 (en) | 2006-04-10 | 2014-03-05 | Abbott Biotechnology Ltd. | Uses and compositions for treatment of rheumatoid arthritis |
EP2666479A2 (en) | 2006-04-10 | 2013-11-27 | Abbott Biotechnology Ltd | Uses and compositions for treatment of juvenile rheumatoid arthritis |
EP2666472A2 (en) | 2006-04-10 | 2013-11-27 | Abbott Biotechnology Ltd | Uses and compositions for treatment of psoriatic arthritis |
US10529441B2 (en) | 2006-05-03 | 2020-01-07 | Population Bio, Inc. | Evaluating genetic disorders |
US10210306B2 (en) | 2006-05-03 | 2019-02-19 | Population Bio, Inc. | Evaluating genetic disorders |
US10522240B2 (en) | 2006-05-03 | 2019-12-31 | Population Bio, Inc. | Evaluating genetic disorders |
US8304451B2 (en) | 2006-05-03 | 2012-11-06 | President And Fellows Of Harvard College | Histone deacetylase and tubulin deacetylase inhibitors |
EP2447282A2 (en) | 2006-05-30 | 2012-05-02 | Genentech, Inc. | Anti-CD22 Antibodies, their Immunoconjugates and uses thereof |
EP2446904A2 (en) | 2006-05-30 | 2012-05-02 | Genentech, Inc. | Anti-CD22 antibodies, their immunoconjugates and uses thereof |
US7803377B2 (en) | 2006-06-06 | 2010-09-28 | Genentech, Inc. | Anti-DLL4 antibodies and methods using same |
US9486584B2 (en) | 2006-06-30 | 2016-11-08 | Abbvie Biotechnology Ltd. | Automatic injection device |
EP3034607A1 (en) | 2006-07-05 | 2016-06-22 | Catalyst Biosciences, Inc. | Protease screening methods and proteases identified thereby |
EP2402438A2 (en) | 2006-07-05 | 2012-01-04 | Catalyst Biosciences, Inc. | Protease screening methods and proteases identified thereby |
EP2402437A2 (en) | 2006-07-05 | 2012-01-04 | Catalyst Biosciences, Inc. | Protease screening methods and proteases identified thereby |
US11827720B2 (en) | 2006-07-05 | 2023-11-28 | F-Star Therapeutics Limited | Multivalent immunoglobulins |
EP2511301A2 (en) | 2006-08-04 | 2012-10-17 | Medimmune Limited | Human antibodies to ERBB2 |
EP3339445A1 (en) | 2006-09-08 | 2018-06-27 | AbbVie Bahamas Ltd. | Interleukin -13 binding proteins |
US10086076B2 (en) | 2006-09-08 | 2018-10-02 | Abbvie Inc. | Interleukin-13 binding proteins |
EP3524685A1 (en) | 2006-09-08 | 2019-08-14 | AbbVie Bahamas Ltd. | Interleukin -13 binding proteins |
EP3910065A1 (en) | 2006-09-08 | 2021-11-17 | AbbVie Bahamas Ltd. | Interleukin -13 binding proteins |
US11344621B2 (en) | 2006-09-08 | 2022-05-31 | Abbvie, Inc. | Interleukin-13 binding proteins |
EP3569245A1 (en) | 2006-09-26 | 2019-11-20 | Genmab A/S | Combination treatment of cd38-expressing tumors |
EP3753576A1 (en) | 2006-09-26 | 2020-12-23 | Genmab A/S | Combination treatment of cd38-expressing tumors |
US7744890B2 (en) | 2006-10-12 | 2010-06-29 | Wyeth Llc | Methods and compositions with reduced opalescence |
EP2845866A1 (en) | 2006-10-27 | 2015-03-11 | Genentech, Inc. | Antibodies and immunoconjugates and uses therefor |
WO2008052187A2 (en) | 2006-10-27 | 2008-05-02 | Genentech. Inc. | Antibodies and immunoconjugates and uses therefor |
EP2395077A1 (en) | 2006-11-03 | 2011-12-14 | Wyeth LLC | Glycolysis-inhibiting substances in cell culture |
US8192951B2 (en) | 2006-11-03 | 2012-06-05 | Wyeth Llc | Glycolysis-inhibiting substances in cell culture |
EP2514439A1 (en) | 2006-11-15 | 2012-10-24 | Functional Genetics, Inc. | Anti-TSG101antibodies and their uses for treatment of viral infections |
US7964708B2 (en) | 2006-11-15 | 2011-06-21 | Limin Li | Anti-TSG101 antibodies and their uses for treatment of viral infections |
US8796423B2 (en) | 2006-11-15 | 2014-08-05 | Eli Lilly And Company | Anti-TSG101 antibodies and their uses for treatment of viral infections |
US7488807B2 (en) | 2006-11-22 | 2009-02-10 | 3M Innovative Properties Company | Antibody with protein A selectivity |
US9951125B2 (en) | 2006-11-30 | 2018-04-24 | Abbvie Inc. | Aβ conformer selective anti-Aβ globulomer monoclonal antibodies |
US8637244B2 (en) | 2006-12-05 | 2014-01-28 | Decode Genetics Ehf. | Genetic markers for risk management of atrial fibrillation, atrial flutter, and stroke |
EP3124045A2 (en) | 2006-12-20 | 2017-02-01 | Xoma (Us) Llc | Treatment of il-1 beta related diseases |
WO2008083174A2 (en) | 2006-12-27 | 2008-07-10 | Emory University | Compositions and methods for the treatment of infections and tumors |
EP3064220A2 (en) | 2006-12-27 | 2016-09-07 | Emory University | Compositions and methods for the treatment of infections and tumors |
EP2133365A2 (en) | 2006-12-27 | 2009-12-16 | Emory University | Compositions and methods for the treatment of infections and tumors |
EP3721903A1 (en) | 2006-12-27 | 2020-10-14 | Emory University | Compositions and methods for the treatment of infections and tumors |
US8324350B2 (en) | 2006-12-29 | 2012-12-04 | Abbott Laboratories | Dual-specific IL-1α/IL-1β antibodies |
EP2839743A1 (en) | 2007-01-16 | 2015-02-25 | Abbvie Inc. | Methods for treating psoriasis |
US7776331B1 (en) | 2007-01-16 | 2010-08-17 | Abbott Laboratories | Methods of treating plaque psoriasis |
US9051368B2 (en) | 2007-01-16 | 2015-06-09 | Abbvie, Inc. | Methods for treating psoriasis by administering an antibody which binds an epitope of the p40 subunit of IL-12 and/or IL-23 |
US8865400B2 (en) | 2007-02-07 | 2014-10-21 | Decode Genetics Ehf. | Genetic variants contributing to risk of prostate cancer |
US9617597B2 (en) | 2007-02-21 | 2017-04-11 | Decode Genetics Ehf | Genetic susceptibility variants associated with cardiovascular disease |
US11673938B2 (en) | 2007-03-22 | 2023-06-13 | Heptares Therapeutics Limited | Mutant G-protein coupled receptors and methods for selecting them |
US8785135B2 (en) | 2007-03-22 | 2014-07-22 | Heptares Therapeutics Limited | Mutant G-protein coupled receptors and methods for selecting them |
US10317393B2 (en) | 2007-03-23 | 2019-06-11 | Academia Sinica | Alkynyl sugar analogs for labeling and visualization of glycoconjugates in cells |
US8940873B2 (en) | 2007-03-29 | 2015-01-27 | Abbvie Inc. | Crystalline anti-human IL-12 antibodies |
US8168760B2 (en) | 2007-03-29 | 2012-05-01 | Abbott Laboratories | Crystalline anti-human IL-12 antibodies |
US8404819B2 (en) | 2007-03-29 | 2013-03-26 | Abbvie Inc. | Crystalline anti-human IL-12 antibodies |
US7867494B2 (en) | 2007-04-02 | 2011-01-11 | Amgen Fremont Inc. | Anti-IgE antibodies |
EP2481797A1 (en) | 2007-04-13 | 2012-08-01 | Catalyst Biosciences, Inc. | Modified factor VII polypeptides and uses thereof |
EP2535425A1 (en) | 2007-05-25 | 2012-12-19 | Decode Genetics EHF. | Variantes génétiques sur les chr 10q26 utilisées comme marqueurs dans l'évaluation, le diagnostic, le pronostic et le traitement d'un risque de cancer du sein |
US8580501B2 (en) | 2007-05-25 | 2013-11-12 | Decode Genetics Ehf. | Genetic variants on chr 5p12 and 10q26 as markers for use in breast cancer risk assessment, diagnosis, prognosis and treatment |
WO2008154543A2 (en) | 2007-06-11 | 2008-12-18 | Abbott Biotechnology Ltd. | Methods for treating juvenile idiopathic arthritis |
US8138313B2 (en) | 2007-06-15 | 2012-03-20 | Deutsches Krebsforschungszentrum Stiftung Des Offentlichen Rechts | Treatment of tumors using specific anti-L1 antibody |
US9260521B2 (en) | 2007-06-15 | 2016-02-16 | Medigene Ag | Treatment of tumors using specific anti-L1 antibody |
WO2008151819A2 (en) | 2007-06-15 | 2008-12-18 | Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts | Treatment of tumors using specific anti-l1 antibody |
EP3241842A1 (en) | 2007-06-26 | 2017-11-08 | F-Star Biotechnologische Forschungs- und Entwicklungsges.m.b.H | Display of binding agents |
US8921279B2 (en) | 2007-06-26 | 2014-12-30 | F-Star Biotechnologische Forschungs—und Entwicklungsges. m.b.H | Display of binding agents |
US9651559B2 (en) | 2007-06-26 | 2017-05-16 | F-star Biotechnologische Forschungs— und Entwicklungsges.m.b.H | Display of binding agents |
EP2474557A2 (en) | 2007-07-16 | 2012-07-11 | Genentech, Inc. | Anti-CD79b antibodies and immunoconjugates and methods of use |
EP2502937A2 (en) | 2007-07-16 | 2012-09-26 | Genentech, Inc. | Anti-CD 79b Antibodies And Immunoconjugates And Methods Of Use |
EP2641618A2 (en) | 2007-07-16 | 2013-09-25 | Genentech, Inc. | Humanized anti-CD79B antibodies and immunoconjugates and methods of use |
US9062097B2 (en) | 2007-08-21 | 2015-06-23 | Morpho Sys AG | Methods for the formation of disulphide bonds |
WO2009024593A1 (en) | 2007-08-21 | 2009-02-26 | Morphosys Ag | Improved methods for the formation of disulphide bonds |
EP3173425A1 (en) | 2007-11-30 | 2017-05-31 | Genentech, Inc. | Anti-vegf antibodies |
US8697360B2 (en) | 2007-11-30 | 2014-04-15 | Decode Genetics Ehf. | Genetic variants on CHR 11Q and 6Q as markers for prostate and colorectal cancer predisposition |
EP2851372A1 (en) | 2007-11-30 | 2015-03-25 | Genentech, Inc. | Anti-VEGF antibodies |
EP2065402A1 (en) | 2007-11-30 | 2009-06-03 | Industrial Technology Research Institut | Trimeric collagen scaffold antibodies |
US8748182B2 (en) | 2007-12-08 | 2014-06-10 | Heptares Therapeutics Limited | Mutant proteins and methods for producing them |
US10126313B2 (en) | 2007-12-20 | 2018-11-13 | Heptares Therapeutics Limited | Methods for screening for binding partners of G-protein coupled receptors |
EP2851373A1 (en) | 2007-12-20 | 2015-03-25 | Xoma (Us) Llc | Methods for the treatment of gout |
EP2573563A1 (en) | 2007-12-20 | 2013-03-27 | Heptares Therapeutics Limited | Screening |
US8790933B2 (en) | 2007-12-20 | 2014-07-29 | Heptares Therapeutics Limited | Screening |
WO2009086003A1 (en) | 2007-12-20 | 2009-07-09 | Xoma Technology Ltd. | Methods for the treatment of gout |
US9260505B2 (en) | 2007-12-20 | 2016-02-16 | Heptares Therapeutics Limited | Methods for screening for binding partners of G-protein coupled receptors |
WO2009086539A2 (en) | 2007-12-28 | 2009-07-09 | Elan Pharmaceuticals, Inc. | Treatment and prophylaxis of amyloidosis |
EP3693470A1 (en) | 2007-12-28 | 2020-08-12 | Prothena Therapeutics Limited | Treatment and prophylaxis of amyloidosis |
EP2730659A2 (en) | 2007-12-28 | 2014-05-14 | Elan Pharmaceuticals Inc. | Treatment and Prophylaxis of Amyloidosis |
EP2657253A2 (en) | 2008-01-31 | 2013-10-30 | Genentech, Inc. | Anti-CD79b antibodies and immunoconjugates and methods of use |
US9081020B2 (en) | 2008-02-11 | 2015-07-14 | Heptares Therapeutics Limited | Mutant proteins and methods for selecting them |
US8828657B2 (en) | 2008-02-14 | 2014-09-09 | Decode Genetics Ehf. | Susceptibility variants for lung cancer |
US8697374B2 (en) | 2008-02-28 | 2014-04-15 | 3M Innovative Properties Company | Antibodies to Clostridium difficile spores and uses thereof |
US9605069B2 (en) | 2008-02-29 | 2017-03-28 | AbbVie Deutschland GmbH & Co. KG | Antibodies against the RGM a protein and uses thereof |
EP3309173A1 (en) | 2008-02-29 | 2018-04-18 | AbbVie Deutschland GmbH & Co KG | Monoclonal antibodies against the rgm a protein and uses thereof |
WO2009109572A3 (en) * | 2008-03-03 | 2009-11-12 | Ablynx Nv | Monovalent phage display of single variable domains |
WO2009109572A2 (en) * | 2008-03-03 | 2009-09-11 | Ablynx Nv | Monovalent phage display of single variable domains |
EP2810954A2 (en) | 2008-03-18 | 2014-12-10 | Abbvie Inc. | Methods for treating psoriasis |
US8178092B2 (en) | 2008-03-18 | 2012-05-15 | Abbott Laboratories | Methods of treating psoriasis by administration of antibodies to the p40 subunit of IL-12 and/or IL-23 |
US8945545B2 (en) | 2008-03-18 | 2015-02-03 | Abbvie Inc. | Methods of treating psoriasis by administration of antibodies to the p40 subunit of IL-12 and/or IL-23 |
US8808985B2 (en) | 2008-04-01 | 2014-08-19 | Decode Genetics Ehf. | Susceptibility variants for peripheral arterial disease and abdominal aortic aneurysm |
EP3670538A1 (en) | 2008-04-25 | 2020-06-24 | Dyax Corp. | Antibodies against fcrn and use thereof |
EP3348573A1 (en) | 2008-04-25 | 2018-07-18 | Dyax Corp. | Method of producing antibodies against fcrn and use thereof |
US9260520B2 (en) | 2008-04-25 | 2016-02-16 | Dyax Corp. | Antibodies to FeRn and uses thereof |
EP2899209A1 (en) | 2008-04-29 | 2015-07-29 | Abbvie Inc. | Dual Variable Domain Immunoglobulins and uses thereof |
US9029508B2 (en) | 2008-04-29 | 2015-05-12 | Abbvie Inc. | Dual variable domain immunoglobulins and uses thereof |
US10125197B2 (en) | 2008-05-02 | 2018-11-13 | F-Star Biotechnologische Forschungs-Und Entwicklungsges.M.B.H | Cytotoxic immunoglobulin |
US9255149B2 (en) | 2008-05-02 | 2016-02-09 | F-Star Biotechnologische Forschungs- Und Entwicklungsges.M.B.H | Cytotoxic immunoglobulin |
EP2698165A1 (en) | 2008-05-02 | 2014-02-19 | F-Star Biotechnologische Forschungs - und Entwicklungsges. M.B.H. | Cytotoxic immunoglobulin |
EP2630970A1 (en) | 2008-05-02 | 2013-08-28 | f-star Biotechnologische Forschungs- und Entwicklungsges.m.b.H. | Cytotoxic immunoglobulin |
EP2113255A1 (en) | 2008-05-02 | 2009-11-04 | f-star Biotechnologische Forschungs- und Entwicklungsges.m.b.H. | Cytotoxic immunoglobulin |
US8859738B2 (en) | 2008-05-02 | 2014-10-14 | F-Star Biotechnologische Forschungs- Und Entwicklungsges. M.B.H | Cytotoxic immunoglobulin |
US9394363B2 (en) | 2008-05-09 | 2016-07-19 | AbbVie Deutschland GmbH & Co. KG | Antibodies to receptor of advanced glycation end products (RAGE) and uses thereof |
US8323651B2 (en) | 2008-05-09 | 2012-12-04 | Abbott Laboratories | Antibodies to receptor of advanced glycation end products (RAGE) and uses thereof |
EP3059248A1 (en) | 2008-05-09 | 2016-08-24 | Abbvie Deutschland GmbH & Co. KG | Antibodies to receptor of advanced glycation end products (rage) and uses thereof |
EP2116556A1 (en) | 2008-05-09 | 2009-11-11 | Abbott GmbH & Co. KG | Antibodies to receptor of advanced glycation end products (rage) and uses thereof |
EP2500361A1 (en) | 2008-05-09 | 2012-09-19 | Abbott GmbH & Co. KG | Antibodies to receptor of advanced glycation end products (rage) and uses thereof |
WO2009149185A2 (en) | 2008-06-03 | 2009-12-10 | Abbott Laboratories | Dual variable domain immunoglobulins and uses thereof |
EP3002299A1 (en) | 2008-06-03 | 2016-04-06 | AbbVie Inc. | Dual variable domain immunoglobulins and uses thereof |
US9109026B2 (en) | 2008-06-03 | 2015-08-18 | Abbvie, Inc. | Dual variable domain immunoglobulins and uses thereof |
US9035027B2 (en) | 2008-06-03 | 2015-05-19 | Abbvie Inc. | Dual variable domain immunoglobulins and uses thereof |
US11237165B2 (en) | 2008-06-27 | 2022-02-01 | Merus N.V. | Antibody producing non-human animals |
US8951735B2 (en) | 2008-07-07 | 2015-02-10 | Decode Genetics Ehf. | Genetic variants for breast cancer risk assessment |
US8822645B2 (en) | 2008-07-08 | 2014-09-02 | Abbvie Inc. | Prostaglandin E2 dual variable domain immunoglobulins and uses thereof |
EP2810654A1 (en) | 2008-07-08 | 2014-12-10 | AbbVie Inc. | Prostaglandin E2 binding proteins and uses thereof |
US9745375B2 (en) | 2008-07-09 | 2017-08-29 | Biogen Ma Inc. | Compositions comprising antibodies to LINGO or fragments thereof |
US10274488B2 (en) | 2008-07-15 | 2019-04-30 | Academia Sinica | Glycan arrays on PTFE-like aluminum coated glass slides and related methods |
US8440716B2 (en) | 2008-07-23 | 2013-05-14 | President And Fellows Of Harvard College | Deacetylase inhibitors and uses thereof |
US9434686B2 (en) | 2008-07-23 | 2016-09-06 | President And Fellows Of Harvard College | Deacetylase inhibitors and uses thereof |
US8865868B2 (en) | 2008-08-06 | 2014-10-21 | Novo Nordisk Healthcare Ag | Conjugated proteins with prolonged in vivo efficacy |
US9771574B2 (en) | 2008-09-05 | 2017-09-26 | President And Fellows Of Harvard College | Apparatus for continuous directed evolution of proteins and nucleic acids |
EP3199630A1 (en) | 2008-09-05 | 2017-08-02 | President and Fellows of Harvard College | Continuous directed evolution of proteins and nucleic acids |
US9023594B2 (en) | 2008-09-05 | 2015-05-05 | President And Fellows Of Harvard College | Continuous directed evolution of proteins and nucleic acids |
WO2010039536A2 (en) | 2008-09-23 | 2010-04-08 | President And Fellows Of Harvard College | Sirt4 and uses thereof |
WO2010039533A2 (en) | 2008-09-23 | 2010-04-08 | Wyeth | Methods for predicting production of activating signals by cross-linked binding proteins |
US10370448B2 (en) | 2008-09-26 | 2019-08-06 | Emory University | Human anti-PD-1, PD-L1, and PD-L2 antibodies and uses therefor |
EP3530672A1 (en) | 2008-09-26 | 2019-08-28 | Dana Farber Cancer Institute, Inc. | Human anti-pd-1, pd-l1, and pd-l2 antibodies and uses thereof |
US10011656B2 (en) | 2008-09-26 | 2018-07-03 | Emory University | Human anti-PD-1, PD-L1, and PD-L2 antibodies and uses therefor |
US8552154B2 (en) | 2008-09-26 | 2013-10-08 | Emory University | Anti-PD-L1 antibodies and uses therefor |
US8313942B2 (en) | 2008-09-26 | 2012-11-20 | Wyeth Llc | Compatible display vector systems |
US9102727B2 (en) | 2008-09-26 | 2015-08-11 | Emory University | Human anti-PD-1 antibodies and uses therefor |
US9523092B2 (en) | 2008-09-26 | 2016-12-20 | Wyeth Llc | Compatible display vector systems |
US11261251B2 (en) | 2008-09-26 | 2022-03-01 | Dana-Farber Cancer Institute, Inc. | Human anti-PD-1, PD-L1, and PD-L2 antibodies and uses therefor |
EP3335728A1 (en) | 2008-10-10 | 2018-06-20 | Children's Medical Center Corporation | Biochemically stabilized hiv-1 env trimer vaccine |
WO2010045315A1 (en) | 2008-10-14 | 2010-04-22 | Dyax Corp. | Use of igf-ii/igf-iie binding for the treatment and prevention of systemic sclerosis associated pulmonary fibrosis |
EP2921501A1 (en) | 2008-10-20 | 2015-09-23 | Abbvie Inc. | Isolation and purification of antibodies using Protein A affinity chromatography |
EP3011953A1 (en) | 2008-10-29 | 2016-04-27 | Ablynx N.V. | Stabilised formulations of single domain antigen binding molecules |
US9393304B2 (en) | 2008-10-29 | 2016-07-19 | Ablynx N.V. | Formulations of single domain antigen binding molecules |
EP4104821A1 (en) | 2008-10-29 | 2022-12-21 | Ablynx N.V. | Formulations of single domain antigen binding molecules |
EP3199553A1 (en) | 2008-10-29 | 2017-08-02 | China Synthetic Rubber Corporation | Methods and agents for the diagnosis and treatment of hepatocellular carcinoma |
US11370835B2 (en) | 2008-10-29 | 2022-06-28 | Ablynx N.V. | Methods for purification of single domain antigen binding molecules |
US9993552B2 (en) | 2008-10-29 | 2018-06-12 | Ablynx N.V. | Formulations of single domain antigen binding molecules |
US10118962B2 (en) | 2008-10-29 | 2018-11-06 | Ablynx N.V. | Methods for purification of single domain antigen binding molecules |
WO2010062995A2 (en) | 2008-11-26 | 2010-06-03 | Five Prime Therapeutics, Inc. | Compositions and methods for regulating collagen and smooth muscle actin expression by serpine2 |
WO2010063011A2 (en) | 2008-11-28 | 2010-06-03 | Emory University | Methods for the treatment of infections and tumors |
WO2010080985A1 (en) | 2009-01-08 | 2010-07-15 | Dana-Farber Cancer Institute, Inc. | Compositions and methods for induced brown fat differentiation |
US8513192B2 (en) | 2009-01-22 | 2013-08-20 | Novo Nordisk A/S | Stable growth hormone compounds resistant to proteolytic degradation |
WO2010084173A1 (en) | 2009-01-22 | 2010-07-29 | Novo Nordisk Health Care Ag | Stable growth hormone compounds |
US8383778B2 (en) | 2009-01-29 | 2013-02-26 | Abbvie Inc. | IL-1 binding proteins |
USRE45763E1 (en) | 2009-02-24 | 2015-10-20 | Abbott Laboratories | Antibodies to troponin I and methods of use thereof |
WO2010099079A1 (en) | 2009-02-24 | 2010-09-02 | Abbott Laboratories | Antibodies to troponin i and methods of use thereof |
US8030026B2 (en) | 2009-02-24 | 2011-10-04 | Abbott Laboratories | Antibodies to troponin I and methods of use thereof |
EP2853540A1 (en) | 2009-02-24 | 2015-04-01 | Abbott Laboratories | Antibodies to troponin I and methods of use therof |
WO2010102167A1 (en) | 2009-03-05 | 2010-09-10 | Becton, Dickinson And Company | Matrix metalloproteinase-7 (mmp-7) monoclonal antibodies and methods for their use in the detection of ovarian cancer |
EP2810652A2 (en) | 2009-03-05 | 2014-12-10 | AbbVie Inc. | IL-17 binding proteins |
EP2772269A2 (en) | 2009-03-05 | 2014-09-03 | Abbvie Inc. | IL-17 binding proteins |
US9663587B2 (en) | 2009-03-05 | 2017-05-30 | Abbvie Inc. | IL-17 binding proteins |
WO2010102177A1 (en) | 2009-03-06 | 2010-09-10 | Becton, Dickinson And Company | Glycodelin monoclonal antibodies and methods for their use in the detection of ovarian cancer |
US9161977B2 (en) | 2009-03-25 | 2015-10-20 | F. Hoffmann-La Roche Ag | Anti-FGFR3 antibodies and methods using same |
US8710189B2 (en) | 2009-03-25 | 2014-04-29 | Genentech, Inc. | Anti-FGFR3 antibodies and methods using same |
US10287356B2 (en) | 2009-03-25 | 2019-05-14 | Genentech, Inc. | Anti-FGFR3 antibodies and methods using same |
US9499623B2 (en) | 2009-03-25 | 2016-11-22 | Genentech, Inc. | Anti-FGFR3 antibodies and methods using same |
WO2010111367A1 (en) | 2009-03-25 | 2010-09-30 | Genentech, Inc. | Anti-fgfr3 antibodies and methods using same |
EP2679600A1 (en) | 2009-03-25 | 2014-01-01 | Genentech, Inc. | Anti-FGFR3 antibodies and methods using same |
US11401333B2 (en) | 2009-03-25 | 2022-08-02 | Genentech, Inc. | Anti-FGFR3 antibodies and methods using same |
US8410250B2 (en) | 2009-03-25 | 2013-04-02 | Genentech, Inc. | Anti-FGFR3 antibodies and methods using same |
US10000571B2 (en) | 2009-03-25 | 2018-06-19 | Genentech, Inc. | Anti-FGFR3 antibodies and methods using same |
WO2010120561A1 (en) | 2009-04-01 | 2010-10-21 | Genentech, Inc. | Anti-fcrh5 antibodies and immunoconjugates and methods of use |
US8795963B2 (en) | 2009-04-03 | 2014-08-05 | Decode Genetics Ehf. | Genetic markers for risk management of atrial fibrillation and stroke |
EP2799453A1 (en) | 2009-04-29 | 2014-11-05 | The Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc. | ERG monoclonal antibodies |
US9561328B2 (en) | 2009-04-29 | 2017-02-07 | Abbvie Biotechnology Ltd | Automatic injection device |
EP2261242A1 (en) | 2009-06-10 | 2010-12-15 | Universite Catholique De Louvain | Aspartate-N-acetyltransferase enzyme, diagnostic method and therapeutic method |
US8703915B2 (en) | 2009-06-22 | 2014-04-22 | Heptares Therapeutics Limited | Mutant proteins and methods for producing them |
EP2272979A1 (en) | 2009-06-30 | 2011-01-12 | Centre National de la Recherche Scientifique (CNRS) | Method for testing a subject thought to be predisposed to having cancer |
WO2011003996A1 (en) | 2009-07-09 | 2011-01-13 | F. Hoffmann-La Roche Ag | In vivo tumor vasculature imaging |
US8796182B2 (en) | 2009-07-10 | 2014-08-05 | Decode Genetics Ehf. | Genetic markers associated with risk of diabetes mellitus |
WO2011014457A1 (en) | 2009-07-27 | 2011-02-03 | Genentech, Inc. | Combination treatments |
US9259476B2 (en) | 2009-07-31 | 2016-02-16 | Wayne State University | Monophosphorylated lipid A derivatives |
US8809285B2 (en) | 2009-07-31 | 2014-08-19 | Wayne State University | Monophosphorylated lipid A derivatives |
US8841249B2 (en) | 2009-08-06 | 2014-09-23 | Novo Nordisk A/S | Growth hormones with prolonged in-vivo efficacy |
US8716344B2 (en) | 2009-08-11 | 2014-05-06 | President And Fellows Of Harvard College | Class- and isoform-specific HDAC inhibitors and uses thereof |
US10059657B2 (en) | 2009-08-11 | 2018-08-28 | President And Fellows Of Harvard College | Class-and isoform-specific HDAC inhibitors and uses thereof |
US9540317B2 (en) | 2009-08-11 | 2017-01-10 | President And Fellows Of Harvard College | Class- and isoform-specific HDAC inhibitors and uses thereof |
EP3029070A1 (en) | 2009-08-29 | 2016-06-08 | AbbVie Inc. | Therapeutic dll4 binding proteins |
US9469688B2 (en) | 2009-08-29 | 2016-10-18 | Abbvie Inc. | Therapeutic DLL4 binding proteins |
WO2011025964A2 (en) | 2009-08-29 | 2011-03-03 | Abbott Laboratories | Therapeutic dll4 binding proteins |
US8623358B2 (en) | 2009-08-29 | 2014-01-07 | Abbvie Inc. | Therapeutic DLL4 binding proteins |
US9132190B2 (en) | 2009-08-29 | 2015-09-15 | Abbvie Inc. | Therapeutic DLL4 binding proteins |
US8586714B2 (en) | 2009-09-01 | 2013-11-19 | Abbvie, Inc. | Dual variable domain immunoglobulins and uses thereof |
WO2011028950A1 (en) | 2009-09-02 | 2011-03-10 | Genentech, Inc. | Mutant smoothened and methods of using the same |
US8557239B2 (en) | 2009-09-14 | 2013-10-15 | Abbvie Inc. | Methods for treating psoriasis using antibodies that bind to the P40 subunit of IL-12 and/or IL-23 |
WO2011035205A2 (en) | 2009-09-18 | 2011-03-24 | Calmune Corporation | Antibodies against candida, collections thereof and methods of use |
EP2957296A1 (en) | 2009-09-25 | 2015-12-23 | Xoma (Us) Llc | Insulin receptor binding antibodies |
EP3187877A1 (en) | 2009-09-25 | 2017-07-05 | XOMA Technology Ltd. | Screening methods |
WO2011038290A2 (en) | 2009-09-25 | 2011-03-31 | The U. S. A., As Represented By The Secretary, Department Of Health And Human Services | Neutralizing antibodies to hiv-1 and their use |
WO2011038302A2 (en) | 2009-09-25 | 2011-03-31 | Xoma Technology Ltd. | Novel modulators |
WO2011036555A1 (en) | 2009-09-25 | 2011-03-31 | University Of Oslo | Multivalent phage display systems and methods |
US9885711B2 (en) | 2009-09-25 | 2018-02-06 | Xoma Technology Ltd. | Screening methods |
WO2011038301A2 (en) | 2009-09-25 | 2011-03-31 | Xoma Technology Ltd. | Screening methods |
WO2011041584A2 (en) | 2009-09-30 | 2011-04-07 | President And Fellows Of Harvard College | Methods for modulation of autophagy through the modulation of autophagy-enhancing gene products |
WO2011041582A2 (en) | 2009-09-30 | 2011-04-07 | President And Fellows Of Harvard College | Methods for modulation of autophagy through the modulation of autophagy-inhibiting gene products |
US8716450B2 (en) | 2009-10-15 | 2014-05-06 | Abbvie Inc. | Dual variable domain immunoglobulins and uses thereof |
US9975948B2 (en) | 2009-10-20 | 2018-05-22 | Abbvie, Inc. | Isolation and purification of anti-IL-13 antibodies using protein A affinity chromatography |
US9266950B2 (en) | 2009-10-20 | 2016-02-23 | Abbvie Inc. | Isolation and purification of anti-IL-13 antibodies using protein a affinity chromatography |
US11390668B2 (en) | 2009-10-20 | 2022-07-19 | Abbvie Inc. | Isolation and purification of anti-IL-13 antibodies using protein a affinity chromatography |
EP3037104A1 (en) | 2009-10-20 | 2016-06-29 | AbbVie Inc. | Isolation and purification of anti-il-13 antibodies using protein a affinity chromatography |
WO2011050188A1 (en) | 2009-10-22 | 2011-04-28 | Genentech, Inc. | Anti-hepsin antibodies and methods using same |
WO2011056497A1 (en) | 2009-10-26 | 2011-05-12 | Genentech, Inc. | Activin receptor type iib compositions and methods of use |
WO2011056494A1 (en) | 2009-10-26 | 2011-05-12 | Genentech, Inc. | Activin receptor-like kinase-1 antagonist and vegfr3 antagonist combinations |
WO2011056502A1 (en) | 2009-10-26 | 2011-05-12 | Genentech, Inc. | Bone morphogenetic protein receptor type ii compositions and methods of use |
WO2011053538A1 (en) | 2009-10-27 | 2011-05-05 | Exxonmobil Research And Engineering Company | Multi-stage processes and control thereof |
US8722855B2 (en) | 2009-10-28 | 2014-05-13 | Abbvie Inc. | Dual variable domain immunoglobulins and uses thereof |
US9067996B2 (en) | 2009-10-31 | 2015-06-30 | Abbvie Inc. | Antibodies to receptor for advanced glycation end products (RAGE) and uses thereof |
US8420083B2 (en) | 2009-10-31 | 2013-04-16 | Abbvie Inc. | Antibodies to receptor for advanced glycation end products (RAGE) and uses thereof |
WO2011057120A1 (en) | 2009-11-05 | 2011-05-12 | Genentech, Inc. | Methods and composition for secretion of heterologous polypeptides |
WO2011058087A1 (en) | 2009-11-11 | 2011-05-19 | Gentian As | Immunoassay for assessing related analytes of different origin |
EP3168232A1 (en) | 2009-11-13 | 2017-05-17 | Dana-Farber Cancer Institute, Inc. | Compositions, kits, and methods for the diagnosis, prognosis, monitoring, treatment and modulation of post-transplant lymphoproliferative disorders and hypoxia associated angiogenesis disorders using galectin-1 |
US11377485B2 (en) | 2009-12-02 | 2022-07-05 | Academia Sinica | Methods for modifying human antibodies by glycan engineering |
US11267870B2 (en) | 2009-12-02 | 2022-03-08 | Academia Sinica | Methods for modifying human antibodies by glycan engineering |
US10087236B2 (en) | 2009-12-02 | 2018-10-02 | Academia Sinica | Methods for modifying human antibodies by glycan engineering |
US9175075B2 (en) | 2009-12-08 | 2015-11-03 | AbbVie Deutschland GmbH & Co. KG | Methods of treating retinal nerve fiber layer degeneration with monoclonal antibodies against a retinal guidance molecule (RGM) protein |
WO2011070045A1 (en) | 2009-12-08 | 2011-06-16 | Abbott Gmbh & Co. Kg | Monoclonal antibodies against the rgm a protein for use in the treatment of retinal nerve fiber layer degeneration |
WO2011071577A1 (en) | 2009-12-11 | 2011-06-16 | Genentech, Inc. | Anti-vegf-c antibodies and methods using same |
WO2011084750A1 (en) | 2009-12-21 | 2011-07-14 | Genentech, Inc. | Antibody formulation |
EP3616719A1 (en) | 2009-12-21 | 2020-03-04 | F. Hoffmann-La Roche AG | Antibody formulation |
WO2011079185A1 (en) | 2009-12-23 | 2011-06-30 | Genentech, Inc. | Anti-bv8 antibodies and uses thereof |
EP4011917A1 (en) | 2010-01-06 | 2022-06-15 | Takeda Pharmaceutical Company Limited | Plasma kallikrein binding proteins |
WO2011085103A2 (en) | 2010-01-06 | 2011-07-14 | Dyax Corp. | Plasma kallikrein binding proteins |
EP3459564A1 (en) | 2010-01-06 | 2019-03-27 | Dyax Corp. | Plasma kallikrein binding proteins |
WO2011088163A1 (en) | 2010-01-14 | 2011-07-21 | President And Fellows Of Harvard College | Methods for modulating skeletal remodeling and patterning by modulating shn2 activity, shn3 activity, or shn2 and shn3 activity in combination |
WO2011089250A3 (en) * | 2010-01-22 | 2011-10-13 | Novo Nordisk Health Care Ag | Stable growth hormone compounds |
WO2011089250A2 (en) | 2010-01-22 | 2011-07-28 | Novo Nordisk Health Care Ag | Stable growth hormone compounds |
US9211342B2 (en) | 2010-01-22 | 2015-12-15 | Novo Nordisk Healthcare Ag | Stable growth hormone compounds resistant to proteolytic degradation |
WO2011091134A2 (en) | 2010-01-22 | 2011-07-28 | Dana-Farber Cancer Institute, Inc. | Compositions,kits, and methods for identification, assessment, prevention, and therapy of metabolic disorders |
US9695226B2 (en) | 2010-01-22 | 2017-07-04 | Novo Nordisk Healthcare Ag | Growth hormones with prolonged in-vivo efficacy |
US8779109B2 (en) | 2010-01-22 | 2014-07-15 | Novo Nordisk Health Care Ag | Growth hormones with prolonged in-vivo efficacy |
WO2011097301A2 (en) | 2010-02-02 | 2011-08-11 | Abbott Biotechnology Ltd. | METHODS AND COMPOSITIONS FOR PREDICTING RESPONSIVENESS TO TREATMENT WITH TNF-α INHIBITOR |
WO2011095894A2 (en) | 2010-02-04 | 2011-08-11 | Jichi Medical University | Identification, assessment, and therapy of cancers with innate or acquired resistance to alk inhibitors |
EP3680253A2 (en) | 2010-03-02 | 2020-07-15 | AbbVie Inc. | Therapeutic dll4 binding proteins |
US9115195B2 (en) | 2010-03-02 | 2015-08-25 | Abbvie Inc. | Therapeutic DLL4 binding proteins |
US9469689B2 (en) | 2010-03-02 | 2016-10-18 | Abbvie Inc. | Therapeutic DLL4 binding proteins |
EP3072904A1 (en) | 2010-03-02 | 2016-09-28 | Abbvie Inc. | Therapeutic dll4 binding proteins |
EP4012714A1 (en) | 2010-03-23 | 2022-06-15 | Iogenetics, LLC. | Bioinformatic processes for determination of peptide binding |
WO2011119484A1 (en) | 2010-03-23 | 2011-09-29 | Iogenetics, Llc | Bioinformatic processes for determination of peptide binding |
US10338069B2 (en) | 2010-04-12 | 2019-07-02 | Academia Sinica | Glycan arrays for high throughput screening of viruses |
US9822171B2 (en) | 2010-04-15 | 2017-11-21 | AbbVie Deutschland GmbH & Co. KG | Amyloid-beta binding proteins |
WO2011130377A2 (en) | 2010-04-15 | 2011-10-20 | Abbott Laboratories | Amyloid-beta binding proteins |
US9447184B2 (en) | 2010-05-14 | 2016-09-20 | Abbvie Inc. | IL-1 binding proteins |
WO2011143562A2 (en) | 2010-05-14 | 2011-11-17 | Abbott Laboratories | Il-1 binding proteins |
US8771966B2 (en) | 2010-06-03 | 2014-07-08 | Genentech, Inc. | Immuno-PET imaging of antibodies and immunoconjugates and uses therefor |
WO2011153346A1 (en) | 2010-06-03 | 2011-12-08 | Genentech, Inc. | Immuno-pet imaging of antibodies and immunoconjugates and uses therefor |
WO2011153477A2 (en) | 2010-06-03 | 2011-12-08 | Abbott Biotechnology Ltd. | Uses and compositions for treatment of hidradenitis suppurativa (hs) |
WO2012047324A2 (en) | 2010-06-10 | 2012-04-12 | President And Fellows Of Harvard College | Systems and methods for amplification and phage display |
US9405884B2 (en) | 2010-06-16 | 2016-08-02 | Abbvie Inc. | Methods and systems for the analysis of protein samples |
US9170262B2 (en) | 2010-06-16 | 2015-10-27 | Abbvie, Inc. | Comparison of protein samples |
WO2012006500A2 (en) | 2010-07-08 | 2012-01-12 | Abbott Laboratories | Monoclonal antibodies against hepatitis c virus core protein |
EP2921177A2 (en) | 2010-07-09 | 2015-09-23 | AbbVie Inc. | Dual variable domain immunoglobulins and uses thereof |
WO2012007880A2 (en) | 2010-07-16 | 2012-01-19 | Ablynx Nv | Modified single domain antigen binding molecules and uses thereof |
WO2012010516A1 (en) | 2010-07-22 | 2012-01-26 | Novo Nordisk Health Care Ag | Growth hormone conjugates |
US11788142B2 (en) | 2010-08-02 | 2023-10-17 | Population Bio, Inc. | Compositions and methods for discovery of causative mutations in genetic disorders |
US10059997B2 (en) | 2010-08-02 | 2018-08-28 | Population Bio, Inc. | Compositions and methods for discovery of causative mutations in genetic disorders |
EP3252072A2 (en) | 2010-08-03 | 2017-12-06 | AbbVie Inc. | Dual variable domain immunoglobulins and uses thereof |
US9493560B2 (en) | 2010-08-03 | 2016-11-15 | Abbvie Inc. | Dual variable domain immunoglobulins and uses thereof |
US8735546B2 (en) | 2010-08-03 | 2014-05-27 | Abbvie Inc. | Dual variable domain immunoglobulins and uses thereof |
WO2012019061A2 (en) | 2010-08-05 | 2012-02-09 | Stem Centrx, Inc. | Novel effectors and methods of use |
WO2012020072A1 (en) | 2010-08-12 | 2012-02-16 | Westfälische Wilhelms-Universität Muenster | Anti-syndecan-4 antibodies |
EP2420250A1 (en) | 2010-08-13 | 2012-02-22 | Universitätsklinikum Münster | Anti-Syndecan-4 antibodies |
US9062101B2 (en) | 2010-08-14 | 2015-06-23 | AbbVie Deutschland GmbH & Co. KG | Amyloid-beta binding proteins |
US10047121B2 (en) | 2010-08-14 | 2018-08-14 | AbbVie Deutschland GmbH & Co. KG | Amyloid-beta binding proteins |
US9505829B2 (en) | 2010-08-19 | 2016-11-29 | Zoetis Belgium S.A. | Anti-NGF antibodies and their use |
US10093725B2 (en) | 2010-08-19 | 2018-10-09 | Zoetis Belgium S.A. | Anti-NGF antibodies and their use |
EP3333188A1 (en) | 2010-08-19 | 2018-06-13 | Zoetis Belgium S.A. | Anti-ngf antibodies and their use |
WO2012024650A2 (en) | 2010-08-19 | 2012-02-23 | Abbott Laboratories | Anti-ngf antibodies and their use |
US10125192B2 (en) | 2010-08-19 | 2018-11-13 | Zoetis Belgium S.A. | Caninized anti-NGF antibodies and their use |
EP4056589A1 (en) | 2010-08-19 | 2022-09-14 | Zoetis Belgium S.A. | Anti-ngf antibodies and their use |
US9046513B2 (en) | 2010-08-26 | 2015-06-02 | Abbvie Inc. | Dual variable domain immunoglobulins and uses thereof |
WO2012027723A1 (en) | 2010-08-27 | 2012-03-01 | Stem Centrx, Inc | Notum protein modulators and methods of use |
WO2012031273A2 (en) | 2010-09-03 | 2012-03-08 | Stem Centrx, Inc. | Novel modulators and methods of use |
WO2012040041A1 (en) | 2010-09-20 | 2012-03-29 | Abbott Laboratories | Purification of antibodies using simulated moving bed chromatography |
EP2446898A1 (en) | 2010-09-30 | 2012-05-02 | Laboratorios Del. Dr. Esteve, S.A. | Use of growth hormone to enhance the immune response in immunosuppressed patients |
WO2012041981A2 (en) | 2010-09-30 | 2012-04-05 | Laboratorios Del Dr. Esteve, S.A. | Use of growth hormone to enhance the immune response in immunosuppressed patients |
WO2012044921A1 (en) | 2010-10-01 | 2012-04-05 | St. Jude Children's Research Hospital | Methods and compositions for typing molecular subgroups of medulloblastoma |
WO2012047968A2 (en) | 2010-10-05 | 2012-04-12 | Genentech, Inc. | Mutant smoothened and methods of using the same |
WO2012052391A1 (en) | 2010-10-19 | 2012-04-26 | Glaxo Group Limited | Polypeptide with jmjd3 catalytic activity |
WO2012068463A2 (en) | 2010-11-18 | 2012-05-24 | Beth Israel Deaconess Medicall Center, Inc. | Methods of treating obesity by inhibiting nicotinamide n-methyl transferase (nnmt) |
WO2012078813A2 (en) | 2010-12-08 | 2012-06-14 | Stem Centrx, Inc. | Novel modulators and methods of use |
WO2012118547A1 (en) | 2010-12-08 | 2012-09-07 | Stem Centrx, Inc. | Novel modulators and methods of use |
WO2012088094A2 (en) | 2010-12-21 | 2012-06-28 | Abbott Laboratories | Il-1 binding proteins |
WO2012121775A2 (en) | 2010-12-21 | 2012-09-13 | Abbott Laboratories | Dual variable domain immunoglobulins and uses thereof |
US11214792B2 (en) | 2010-12-22 | 2022-01-04 | President And Fellows Of Harvard College | Continuous directed evolution |
US9394537B2 (en) | 2010-12-22 | 2016-07-19 | President And Fellows Of Harvard College | Continuous directed evolution |
US10336997B2 (en) | 2010-12-22 | 2019-07-02 | President And Fellows Of Harvard College | Continuous directed evolution |
WO2012092323A1 (en) | 2010-12-28 | 2012-07-05 | Xoma Technology Ltd. | Cell surface display using pdz domains |
WO2012089814A1 (en) | 2010-12-30 | 2012-07-05 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Antigen binding formats for use in therapeutic treatments or diagnostic assays |
WO2012092539A2 (en) | 2010-12-31 | 2012-07-05 | Takeda Pharmaceutical Company Limited | Antibodies to dll4 and uses thereof |
US11565048B2 (en) | 2011-01-24 | 2023-01-31 | Abbvie Biotechnology Ltd. | Automatic injection devices having overmolded gripping surfaces |
US9878102B2 (en) | 2011-01-24 | 2018-01-30 | Abbvie Biotechnology Ltd. | Automatic injection devices having overmolded gripping surfaces |
US9956236B2 (en) | 2011-02-07 | 2018-05-01 | Cornell University | Methods for increasing immune responses using agents that directly bind to and activate IRE-1 |
EP3763388A1 (en) | 2011-02-18 | 2021-01-13 | AbbVie Stemcentrx LLC | Novel modulators and methods of use |
WO2012112943A1 (en) | 2011-02-18 | 2012-08-23 | Stem Centrx, Inc. | Novel modulators and methods of use |
WO2012119129A1 (en) | 2011-03-02 | 2012-09-07 | Berg Biosystems, Llc | Interrogatory cell-based assays and uses thereof |
US9383364B2 (en) | 2011-03-07 | 2016-07-05 | University Of Louisville Research Foundation, Inc. | Predictive marker of DNMT1 inhibitor therapeutic efficacy and methods of using the marker |
WO2012125735A1 (en) | 2011-03-15 | 2012-09-20 | Abott Laboratories | An integrated approach to the isolation and purification of antibodies |
WO2012128810A1 (en) | 2011-03-23 | 2012-09-27 | Abbott Laboratories | Methods and systems for the analysis of protein samples |
WO2012131053A1 (en) | 2011-03-30 | 2012-10-04 | Ablynx Nv | Methods of treating immune disorders with single domain antibodies against tnf-alpha |
WO2012134813A1 (en) | 2011-03-31 | 2012-10-04 | St. Jude Children's Research Hospital | Methods and compositions for identifying minimal residual disease in acute lymphoblastic leukemia |
WO2012139058A1 (en) | 2011-04-08 | 2012-10-11 | Biogen Idec Ma Inc. | BIOMARKERS PREDICTIVE OF THERAPEUTIC RESPONSIVENESS TO IFNβ AND USES THEREOF |
WO2012142164A1 (en) | 2011-04-12 | 2012-10-18 | The United States Of America, As Represented By The Secretary, Department Of Health & Human Services | Human monoclonal antibodies that bind insulin-like growth factor (igf) i and ii |
US11739152B2 (en) | 2011-06-02 | 2023-08-29 | Takeda Pharmaceutical Company Limited | Antibodies which bind Fc receptors (FcRn) |
US11014988B2 (en) | 2011-06-02 | 2021-05-25 | Dyax Corp. | Nucleic acids encoding anti-neonatal Fc receptor (FcRn) antibodies |
EP2966089A1 (en) | 2011-06-02 | 2016-01-13 | Dyax Corp. | Fc receptor binding proteins |
US10479834B2 (en) | 2011-06-02 | 2019-11-19 | Dyax Corp. | Fc receptor antibodies and methods of use thereof |
US9862768B2 (en) | 2011-06-02 | 2018-01-09 | Dyax Corp. | Methods of producing antibodies to neonatal Fc receptor (FcRn) |
US9359438B2 (en) | 2011-06-02 | 2016-06-07 | Dyax Corporation | Human neonatal Fc receptor antibodies and methods of use thereof |
EP3954704A1 (en) | 2011-06-03 | 2022-02-16 | XOMA Technology Ltd. | Antibodies specific for tgf-beta |
WO2012167143A1 (en) | 2011-06-03 | 2012-12-06 | Xoma Technology Ltd. | Antibodies specific for tgf-beta |
EP3574919A1 (en) | 2011-07-13 | 2019-12-04 | AbbVie Inc. | Methods and compositions for treating asthma using anti-il-13 antibodies |
EP3564261A1 (en) | 2011-08-23 | 2019-11-06 | Foundation Medicine, Inc. | Kif5b-ret fusion molecules and uses thereof |
WO2013028817A1 (en) | 2011-08-23 | 2013-02-28 | Foundation Medicine , Inc. | Novel kif5b-ret fusion molecules and uses thereof |
WO2013039996A1 (en) | 2011-09-13 | 2013-03-21 | Dana-Farber Cancer Institute, Inc. | Compositions and methods for brown fat induction and activity using fndc5 |
WO2013040142A2 (en) | 2011-09-16 | 2013-03-21 | Iogenetics, Llc | Bioinformatic processes for determination of peptide binding |
WO2013054200A2 (en) | 2011-10-10 | 2013-04-18 | The Hospital For Sick Children | Methods and compositions for screening and treating developmental disorders |
US11339439B2 (en) | 2011-10-10 | 2022-05-24 | The Hospital For Sick Children | Methods and compositions for screening and treating developmental disorders |
WO2013063114A1 (en) | 2011-10-24 | 2013-05-02 | Abbvie Inc. | Immunobinders directed against tnf |
WO2013063095A1 (en) | 2011-10-24 | 2013-05-02 | Abbvie Inc. | Immunobinders directed against sclerostin |
WO2013067268A1 (en) | 2011-11-03 | 2013-05-10 | Tripath Imaging, Inc. | Methods and compositions for preparing samples for immunostaining |
WO2013067451A2 (en) | 2011-11-04 | 2013-05-10 | Population Diagnostics Inc. | Methods and compositions for diagnosing, prognosing, and treating neurological conditions |
US11180807B2 (en) | 2011-11-04 | 2021-11-23 | Population Bio, Inc. | Methods for detecting a genetic variation in attractin-like 1 (ATRNL1) gene in subject with Parkinson's disease |
WO2013068902A1 (en) | 2011-11-08 | 2013-05-16 | Pfizer Inc. | Methods of treating inflammatory disorders using anti-m-csf antibodies |
WO2013078377A1 (en) | 2011-11-23 | 2013-05-30 | Igenica, Inc. | Anti-cd98 antibodies and methods of use thereof |
WO2013080050A2 (en) | 2011-11-30 | 2013-06-06 | Universitaetsklinikum Erlangen | Methods and compositions for determining responsiveness to treatment with a tnf-alpha inhibitor |
US10118958B2 (en) | 2011-12-14 | 2018-11-06 | AbbVie Deutschland GmbH & Co. KG | Composition and method for the diagnosis and treatment of iron-related disorders |
WO2013090633A2 (en) | 2011-12-14 | 2013-06-20 | AbbVie Deutschland GmbH & Co. KG | Composition and method for the diagnosis and treatment of iron-related disorders |
WO2013090635A2 (en) | 2011-12-14 | 2013-06-20 | AbbVie Deutschland GmbH & Co. KG | Composition and method for the diagnosis and treatment of iron-related disorders |
EP3800200A1 (en) | 2011-12-14 | 2021-04-07 | AbbVie Deutschland GmbH & Co. KG | Composition and method for the diagnosis and treatment of iron-related disorders |
US10822403B2 (en) | 2011-12-14 | 2020-11-03 | AbbVie Deutschland GmbH & Co. KG | Composition and method for the diagnosis and treatment of iron-related disorders |
US9636398B2 (en) | 2011-12-14 | 2017-05-02 | AbbVie Deutschland GmbH & Co. KG | Composition and method for the diagnosis and treatment of iron-related disorders |
EP3050900A1 (en) | 2011-12-19 | 2016-08-03 | Xoma (Us) Llc | Methods for treating acne |
WO2013096516A1 (en) | 2011-12-19 | 2013-06-27 | Xoma Technology Ltd. | Methods for treating acne |
US9120870B2 (en) | 2011-12-30 | 2015-09-01 | Abbvie Inc. | Dual specific binding proteins directed against IL-13 and IL-17 |
EP3663314A1 (en) | 2012-01-09 | 2020-06-10 | The Scripps Research Institute | Humanized antibodies with ultralong cdr3s |
WO2013106485A2 (en) | 2012-01-09 | 2013-07-18 | The Scripps Research Institute | Ultralong complementarity determining regions and uses thereof |
WO2013106489A1 (en) | 2012-01-09 | 2013-07-18 | The Scripps Research Institute | Humanized antibodies with ultralong cdr3s |
WO2013112922A1 (en) | 2012-01-27 | 2013-08-01 | AbbVie Deutschland GmbH & Co. KG | Composition and method for diagnosis and treatment of diseases associated with neurite degeneration |
US9102722B2 (en) | 2012-01-27 | 2015-08-11 | AbbVie Deutschland GmbH & Co. KG | Composition and method for the diagnosis and treatment of diseases associated with neurite degeneration |
US9365643B2 (en) | 2012-01-27 | 2016-06-14 | AbbVie Deutschland GmbH & Co. KG | Antibodies that bind to repulsive guidance molecule A (RGMA) |
US10106602B2 (en) | 2012-01-27 | 2018-10-23 | AbbVie Deutschland GmbH & Co. KG | Isolated monoclonal anti-repulsive guidance molecule A antibodies and uses thereof |
EP3653647A1 (en) | 2012-01-27 | 2020-05-20 | AbbVie Deutschland GmbH & Co KG | Composition and method for diagnosis and treatment of diseases associated with neurite degeneration |
EP3369746A1 (en) | 2012-01-27 | 2018-09-05 | AbbVie Deutschland GmbH & Co KG | Composition and method for diagnosis and treatment of diseases associated with neurite degeneration |
WO2013119960A2 (en) | 2012-02-08 | 2013-08-15 | Stem Centrx, Inc. | Novel modulators and methods of use |
US10407724B2 (en) | 2012-02-09 | 2019-09-10 | The Hospital For Sick Children | Methods and compositions for screening and treating developmental disorders |
US11174516B2 (en) | 2012-02-09 | 2021-11-16 | The Hospital For Sick Children | Methods and compositions for screening and treating developmental disorders |
US9155803B1 (en) | 2012-02-24 | 2015-10-13 | Stemcentrx, Inc. | Anti-DLL3 antibody drug conjugates and methods of use |
US9931421B2 (en) | 2012-02-24 | 2018-04-03 | Abbvie Stemcentrx Llc | Methods of delivering DLL3 antibody drug conjugates |
US9878053B2 (en) | 2012-02-24 | 2018-01-30 | Abbvie Stemcentrx Llc | Methods of delivering DLL3 antibody drug conjugates |
US9345784B1 (en) | 2012-02-24 | 2016-05-24 | Stemcentrx, Inc. | Methods of delivering DLL3 antibody drug conjugates |
EP3095797A1 (en) | 2012-02-24 | 2016-11-23 | Stemcentrx, Inc. | Anti dll3 antibodies and methods of use thereof |
US8986972B2 (en) | 2012-02-24 | 2015-03-24 | Stem Centrx, Inc. | Nucleic acid encoding DLL3 antibodies |
US9107961B2 (en) | 2012-02-24 | 2015-08-18 | Stemcentrx, Inc. | Anti-DLL3 antibody drug conjugates for treating cancer |
US9334318B1 (en) | 2012-02-24 | 2016-05-10 | Stemcentrx, Inc. | Multivalent DLL3 antibodies |
US9480757B2 (en) | 2012-02-24 | 2016-11-01 | Abbvie Stemcentrx Llc | Anti-DLL3 antibody drug conjugates |
US9867887B1 (en) | 2012-02-24 | 2018-01-16 | Abbvie Stemcentrx Llc | Anti-DLL3 antibody drug conjugates |
US9173959B1 (en) | 2012-02-24 | 2015-11-03 | Stemcentrx, Inc. | Anti-DLL3 antibody drug conjugates |
US9486537B2 (en) | 2012-02-24 | 2016-11-08 | Abbvie Stemcentrx Llc | Anti-DLL3 antibody drug conjugates |
US9090683B2 (en) | 2012-02-24 | 2015-07-28 | Stemcentrx, Inc. | Methods of detection, diagnosis, and monitoring using anti-DLL3 antibodies |
US11033634B2 (en) | 2012-02-24 | 2021-06-15 | Abbvie Stemcentrx Llc | Light chain variable regions |
US9133271B1 (en) | 2012-02-24 | 2015-09-15 | Stemcentrx, Inc. | Anti-DLL3 antibody drug conjugates and methods of use |
US9089615B2 (en) | 2012-02-24 | 2015-07-28 | Stemcentrx, Inc. | Anti-DLL3 antibodies |
US9861708B2 (en) | 2012-02-24 | 2018-01-09 | Abbvie Stemcentrx Llc | Kits containing DLL3 antibody drug conjugates |
US9089617B2 (en) | 2012-02-24 | 2015-07-28 | Stemcentrx, Inc. | Anti-DLL3 antibody drug conjugates |
US9481727B2 (en) | 2012-02-24 | 2016-11-01 | Abbvie Stemcentrx Llc | Anti-DLL3 antibody drug conjugates |
US9353182B2 (en) | 2012-02-24 | 2016-05-31 | Stemcentrx, Inc. | Anti-DLL3 antibodies |
US9855343B2 (en) | 2012-02-24 | 2018-01-02 | Abbvie Stemcentrx Llc | Anti-DLL3 antibody drug conjugates |
US9764042B1 (en) | 2012-02-24 | 2017-09-19 | Abbvie Stemcentrx Llc | Methods of making DLL3 antibody drug conjugates |
US9937268B2 (en) | 2012-02-24 | 2018-04-10 | Abbvie Stemcentrx Llc | Anti-DLL3 antibody drug conjugates and methods of use |
US9089616B2 (en) | 2012-02-24 | 2015-07-28 | Stemcentrx, Inc. | Anti-DLL3 antibody drug conjugates and methods of use |
US9770518B1 (en) | 2012-02-24 | 2017-09-26 | Abbvie Stemcentrx Llc | Anti-DLL3 antibody drug conjugates |
US9931420B2 (en) | 2012-02-24 | 2018-04-03 | Abbvie Stemcentrx Llc | Methods of making DLL3 antibody drug conjugates |
US10137204B2 (en) | 2012-02-24 | 2018-11-27 | Abbvie Stemcentrx Llc | Anti-DLL3 antibody drug conjugates for treating cancer |
US9352051B1 (en) | 2012-02-24 | 2016-05-31 | Stemcentrx, Inc. | Kits containing DLL3 antibody drug conjugates |
US9775916B1 (en) | 2012-02-24 | 2017-10-03 | Abbvie Stemcentrx Llc | Anti-DLL3 antibody drug conjugates for treating cancer |
US9358304B1 (en) | 2012-02-24 | 2016-06-07 | Stemcentrx, Inc. | Methods of making DLL3 antibody drug conjugates |
US9139659B2 (en) * | 2012-03-28 | 2015-09-22 | Genentech, Inc. | Idiotypic antibodies and uses thereof |
WO2013148373A1 (en) | 2012-03-28 | 2013-10-03 | Genentech, Inc. | Anti-hcmv idiotypic antibodies and uses thereof |
US20130266973A1 (en) * | 2012-03-28 | 2013-10-10 | Genentech, Inc. | Idiotypic antibodies and uses thereof |
WO2013151577A1 (en) | 2012-04-02 | 2013-10-10 | Berg Pharma Llc | Interrogatory cell-based assays and uses thereof |
US10130714B2 (en) | 2012-04-14 | 2018-11-20 | Academia Sinica | Enhanced anti-influenza agents conjugated with anti-inflammatory activity |
WO2013158279A1 (en) | 2012-04-20 | 2013-10-24 | Abbvie Inc. | Protein purification methods to reduce acidic species |
WO2014143184A1 (en) | 2012-04-20 | 2014-09-18 | Abbvie Inc. | Modulated lysine variant species compositions and methods for producing and using the same |
WO2013158275A1 (en) | 2012-04-20 | 2013-10-24 | Abbvie Inc. | Cell culture methods to reduce acidic species |
US9758805B2 (en) | 2012-04-20 | 2017-09-12 | Merus N.V. | Methods and means for the production of Ig-like molecules |
US10752929B2 (en) | 2012-04-20 | 2020-08-25 | Merus N.V. | Methods and means for the production of ig-like molecules |
US11926859B2 (en) | 2012-04-20 | 2024-03-12 | Merus N.V. | Methods and means for the production of Ig-like molecules |
US10337045B2 (en) | 2012-04-20 | 2019-07-02 | Merus N.V. | Methods and means for the production of Ig-like molecules |
US10329596B2 (en) | 2012-04-20 | 2019-06-25 | Merus N.V. | Methods and means for the production of Ig-like molecules |
WO2013158273A1 (en) | 2012-04-20 | 2013-10-24 | Abbvie Inc. | Methods to modulate c-terminal lysine variant distribution |
US9796780B2 (en) | 2012-05-14 | 2017-10-24 | Biogen Ma Inc. | LINGO-2 antagonists for treatment of conditions involving motor neurons |
WO2013177115A2 (en) | 2012-05-21 | 2013-11-28 | Abbvie Inc. | Novel purification of human, humanized, or chimeric antibodies using protein a affinity chromatography |
WO2014143185A1 (en) | 2012-05-24 | 2014-09-18 | Abbvie Inc. | Purification of proteins using hydrophobic interaction chromatography |
WO2013176754A1 (en) | 2012-05-24 | 2013-11-28 | Abbvie Inc. | Novel purification of antibodies using hydrophobic interaction chromatography |
US9617334B2 (en) | 2012-06-06 | 2017-04-11 | Zoetis Services Llc | Caninized anti-NGF antibodies and methods thereof |
US9951128B2 (en) | 2012-06-06 | 2018-04-24 | Zoetis Services Llc | Caninized anti-NGF antibodies and methods thereof |
US9670276B2 (en) | 2012-07-12 | 2017-06-06 | Abbvie Inc. | IL-1 binding proteins |
EP3613765A1 (en) | 2012-08-03 | 2020-02-26 | Dana-Farber Cancer Institute, Inc. | Antibody against repulsive guidance molecule b (rgmb) |
US10214765B2 (en) | 2012-08-18 | 2019-02-26 | Academia Sinica | Cell-permeable probes for identification and imaging of sialidases |
US9737493B2 (en) | 2012-09-07 | 2017-08-22 | University Of Louisville Research Foundation, Inc. | Compositions and methods for modulating DNMT1 inhibitor activity |
US11008614B2 (en) | 2012-09-14 | 2021-05-18 | Population Bio, Inc. | Methods for diagnosing, prognosing, and treating parkinsonism |
WO2014043519A1 (en) | 2012-09-14 | 2014-03-20 | Population Diagnostics Inc. | Methods and compositions for diagnosing, prognosing, and treating neurological conditions |
US9976180B2 (en) | 2012-09-14 | 2018-05-22 | Population Bio, Inc. | Methods for detecting a genetic variation in subjects with parkinsonism |
US11618925B2 (en) | 2012-09-27 | 2023-04-04 | Population Bio, Inc. | Methods and compositions for screening and treating developmental disorders |
US10597721B2 (en) | 2012-09-27 | 2020-03-24 | Population Bio, Inc. | Methods and compositions for screening and treating developmental disorders |
US10233495B2 (en) | 2012-09-27 | 2019-03-19 | The Hospital For Sick Children | Methods and compositions for screening and treating developmental disorders |
EP3750560A2 (en) | 2012-10-09 | 2020-12-16 | Biogen MA Inc. | Combination therapies and uses for treatment of demyelinating disorders |
WO2014058875A2 (en) | 2012-10-09 | 2014-04-17 | Biogen Idec Ma Inc. | Combination therapies and uses for treatment of demyelinating disorders |
WO2014059028A1 (en) | 2012-10-09 | 2014-04-17 | Igenica, Inc. | Anti-c16orf54 antibodies and methods of use thereof |
US9163093B2 (en) | 2012-11-01 | 2015-10-20 | Abbvie Inc. | Anti-DLL4/VEGF dual variable domain immunoglobulin and uses thereof |
US9045551B2 (en) | 2012-11-01 | 2015-06-02 | Abbvie Inc. | Anti-DLL4/VEGF dual variable domain immunoglobulin and uses thereof |
US9944720B2 (en) | 2012-11-01 | 2018-04-17 | Abbvie Inc. | Anti-DLL4/VEGF dual variable domain immunoglobulin and uses thereof |
US11578372B2 (en) | 2012-11-05 | 2023-02-14 | Foundation Medicine, Inc. | NTRK1 fusion molecules and uses thereof |
WO2014071358A2 (en) | 2012-11-05 | 2014-05-08 | Foundation Medicine, Inc. | Novel ntrk1 fusion molecules and uses thereof |
WO2014074942A1 (en) | 2012-11-08 | 2014-05-15 | Illumina, Inc. | Risk variants of alzheimer's disease |
US9951130B2 (en) | 2012-11-08 | 2018-04-24 | Eleven Biotherapeutics, Inc. | IL-6 antagonists and uses thereof |
US11459386B2 (en) | 2012-11-08 | 2022-10-04 | Sesen Bio, Inc. | IL-6 antagonists and uses thereof |
WO2014074905A1 (en) | 2012-11-08 | 2014-05-15 | Eleven Biotherapeutics, Inc. | Il-6 antagonists and uses thereof |
WO2014093396A1 (en) | 2012-12-10 | 2014-06-19 | Biogen Idec Ma Inc. | Anti-blood dendritic cell antigen 2 antibodies and uses thereof |
EP3686218A1 (en) | 2012-12-10 | 2020-07-29 | Biogen MA Inc. | Anti-blood dendritic cell antigen 2 antibodies and uses thereof |
US9550986B2 (en) | 2012-12-21 | 2017-01-24 | Abbvie Inc. | High-throughput antibody humanization |
WO2014100542A1 (en) | 2012-12-21 | 2014-06-26 | Abbvie, Inc. | High-throughput antibody humanization |
US10717965B2 (en) | 2013-01-10 | 2020-07-21 | Gloriana Therapeutics, Inc. | Mammalian cell culture-produced neublastin antibodies |
US11771698B2 (en) | 2013-01-18 | 2023-10-03 | Foundation Medicine, Inc. | Methods of treating cholangiocarcinoma |
EP3939614A1 (en) | 2013-01-18 | 2022-01-19 | Foundation Medicine, Inc. | Methods of treating cholangiocarcinoma |
WO2014113729A2 (en) | 2013-01-18 | 2014-07-24 | Foundation Mecicine, Inc. | Methods of treating cholangiocarcinoma |
WO2014123696A1 (en) | 2013-01-25 | 2014-08-14 | Thymon, Llc | Compositions for selective reduction of circulating bioactive soluble tnf and methods for treating tnf-mediated disease |
US9968687B2 (en) | 2013-02-22 | 2018-05-15 | Abbvie Stemcentrx Llc | Anti-DLL3 antibody drug conjugates |
WO2014130879A2 (en) | 2013-02-22 | 2014-08-28 | Stem Centrx, Inc. | Novel antibody conjugates and uses thereof |
US10478509B2 (en) | 2013-02-22 | 2019-11-19 | Abbvie Stemcentrx Llc | Anti-DLL3 antibody drug conjugates for treating cancer |
EP3556400A1 (en) | 2013-02-22 | 2019-10-23 | AbbVie Stemcentrx LLC | Method of making antidll3-antibody pbd conjugates |
CN105229035A (en) * | 2013-03-11 | 2016-01-06 | 诺和诺德保健股份有限公司 | Growth hormone compound |
WO2014139994A1 (en) * | 2013-03-11 | 2014-09-18 | Novo Nordisk Health Care Ag | Growth hormone compounds |
WO2014160495A1 (en) | 2013-03-13 | 2014-10-02 | Genentech, Inc. | Formulations with reduced oxidation |
US11596620B2 (en) | 2013-03-13 | 2023-03-07 | F. Hoffmann-La Roche Ag | Formulations with reduced oxidation |
US10010611B2 (en) | 2013-03-13 | 2018-07-03 | Genentech, Inc. | Antibody formulations |
EP3744345A1 (en) | 2013-03-13 | 2020-12-02 | F. Hoffmann-La Roche AG | Antibody formulations |
WO2014160497A1 (en) | 2013-03-13 | 2014-10-02 | Genentech, Inc. | Formulations with reduced oxidation |
WO2014160490A1 (en) | 2013-03-13 | 2014-10-02 | Genetech, Inc. | Antibody formulations |
US10925966B2 (en) | 2013-03-13 | 2021-02-23 | Genentech, Inc. | Antibody formulations |
US10653779B2 (en) | 2013-03-13 | 2020-05-19 | Genentech, Inc. | Formulations with reduced oxidation |
EP3564384A1 (en) | 2013-03-14 | 2019-11-06 | Abbott Laboratories | Hcv core lipid binding domain monoclonal antibodies |
US10345311B2 (en) | 2013-03-14 | 2019-07-09 | Abbott Laboratories | Detection methods employing HCV core lipid and DNA binding domain monoclonal antibodies |
WO2014142882A1 (en) | 2013-03-14 | 2014-09-18 | Abbvie Inc. | Protein purification using displacement chromatography |
US9841427B2 (en) | 2013-03-14 | 2017-12-12 | Abbott Laboratories | HCV antigen-antibody combination assay and methods and compositions for use therein |
US10197573B2 (en) | 2013-03-14 | 2019-02-05 | Abbott Laboratories | HCV core lipid binding domain monoclonal antibodies |
WO2014159554A1 (en) | 2013-03-14 | 2014-10-02 | Abbvie Inc. | Low acidic species compositions and methods for producing the same using displacement chromatography |
WO2014158231A1 (en) | 2013-03-14 | 2014-10-02 | Abbvie Inc. | Low acidic species compositions and methods for producing and using the same |
US10444242B2 (en) | 2013-03-14 | 2019-10-15 | Abbott Laboratories | Detection methods employing HCV core lipid and DNA binding domain monoclonal antibodies |
WO2014153056A2 (en) | 2013-03-14 | 2014-09-25 | Parkash Gill | Cancer treatment using antibodies that bing cell surface grp78 |
US9790478B2 (en) | 2013-03-14 | 2017-10-17 | Abbott Laboratories | HCV NS3 recombinant antigens and mutants thereof for improved antibody detection |
US11428694B2 (en) | 2013-03-14 | 2022-08-30 | Abbott Laboratories | Detection methods employing HCV core lipid and DNA binding domain monoclonal antibodies |
EP3916103A1 (en) | 2013-03-14 | 2021-12-01 | Abbott Laboratories | Hcv core lipid binding domain monoclonal antibodies |
WO2014144355A2 (en) | 2013-03-15 | 2014-09-18 | Abbott Laboratories | Anti-gp73 monoclonal antibodies and methods of obtaining the same |
EP3527586A1 (en) | 2013-03-15 | 2019-08-21 | Abbott Laboratories | Anti-gp73 monoclonal antibodies and methods of obtaining the same |
US10829732B2 (en) | 2013-03-15 | 2020-11-10 | Genentech, Inc. | Cell culture compositions with antioxidants and methods for polypeptide production |
US10017732B2 (en) | 2013-03-15 | 2018-07-10 | Genentech, Inc. | Cell culture compositions with antioxidants and methods for polypeptide production |
EP4079760A2 (en) | 2013-03-15 | 2022-10-26 | Sanofi Pasteur Inc. | Antibodies against clostridium difficile toxins and methods of using the same |
US9469686B2 (en) | 2013-03-15 | 2016-10-18 | Abbott Laboratories | Anti-GP73 monoclonal antibodies and methods of obtaining the same |
EP3124499A1 (en) | 2013-03-15 | 2017-02-01 | Abbott Laboratories | Anti-gp73 monoclonal antibodies and methods of obtaining the same |
US10676710B2 (en) | 2013-03-15 | 2020-06-09 | Genentech, Inc. | Cell culture compositions with antioxidants and methods for polypeptide production |
US10308709B2 (en) | 2013-03-15 | 2019-06-04 | Abbott Laboratories | Anti-GP73 monoclonal antibodies and methods of obtaining the same |
US8987418B2 (en) | 2013-03-15 | 2015-03-24 | Abbvie Inc. | Dual specific binding proteins directed against IL-1β and/or IL-17 |
EP3712252A1 (en) | 2013-03-15 | 2020-09-23 | F. Hoffmann-La Roche AG | Cell culture compositions with antioxidants and methods for polypeptide production |
US9062108B2 (en) | 2013-03-15 | 2015-06-23 | Abbvie Inc. | Dual specific binding proteins directed against IL-1 and/or IL-17 |
WO2014151680A1 (en) | 2013-03-15 | 2014-09-25 | Biogen Idec Ma Inc. | Treatment and prevention of acute kidney injury using anti-alpha v beta 5 antibodies |
WO2014144292A2 (en) | 2013-03-15 | 2014-09-18 | Sanofi Pasteur Biologics , Llc | Antibodies against clostridium difficile toxins and methods of using the same |
WO2014145098A1 (en) | 2013-03-15 | 2014-09-18 | Genentech, Inc. | Cell culture compositions with antioxidants and methods for polypeptide production |
US11421023B2 (en) | 2013-03-15 | 2022-08-23 | Abbott Laboratories | Anti-GP73 monoclonal antibodies and methods of obtaining the same |
US9441035B2 (en) | 2013-03-15 | 2016-09-13 | Genentech, Inc. | Cell culture media and methods of antibody production |
US10131873B2 (en) | 2013-03-15 | 2018-11-20 | Genentech, Inc. | Cell culture compositions with antioxidants and methods for polypeptide production |
US11045523B2 (en) | 2013-04-05 | 2021-06-29 | Novo Nordisk Healthcare Ag | Formulation of growth hormone albumin-binder conjugate |
US9499621B2 (en) | 2013-04-08 | 2016-11-22 | Cytodyn, Inc. | Felinized antibodies and methods of treating retroviral infections in felines |
EP3293275A1 (en) | 2013-06-06 | 2018-03-14 | Dana-Farber Cancer Institute, Inc. | Compositions and methods for identification, assessment prevention, and treatment of cancer using pd-l1 isoforms |
US11897946B2 (en) | 2013-06-07 | 2024-02-13 | Duke University | Methods of inhibiting complement factor H (CFH) comprising administering an antibody that binds CFH |
US10183988B2 (en) | 2013-06-07 | 2019-01-22 | Duke University | Anti-Complement factor H antibodies |
US11136380B2 (en) | 2013-06-07 | 2021-10-05 | Duke University | Anti-complement factor H antibodies |
EP3632467A1 (en) | 2013-06-07 | 2020-04-08 | Duke University | Inhibitors of complement factor h |
WO2014197885A2 (en) | 2013-06-07 | 2014-12-11 | Duke University | Inhibitors of complement factor h |
US10086054B2 (en) | 2013-06-26 | 2018-10-02 | Academia Sinica | RM2 antigens and use thereof |
US9981030B2 (en) | 2013-06-27 | 2018-05-29 | Academia Sinica | Glycan conjugates and use thereof |
WO2015010100A2 (en) | 2013-07-18 | 2015-01-22 | Fabrus, Inc. | Humanized antibodies with ultralong complementarity determining regions |
WO2015017146A2 (en) | 2013-07-18 | 2015-02-05 | Fabrus, Inc. | Antibodies with ultralong complementarity determining regions |
WO2015017529A2 (en) | 2013-07-31 | 2015-02-05 | Dana-Farber Cancer Institute, Inc. | Compositions and methods for modulating thermogenesis using pth-related and egf-related molecules |
EP3916081A2 (en) | 2013-08-19 | 2021-12-01 | Biogen MA Inc. | Control of protein glycosylation by culture medium supplementation and cell culture process parameters |
WO2015026846A1 (en) | 2013-08-19 | 2015-02-26 | Biogen Idec Ma Inc. | Control of protein glycosylation by culture medium supplementation and cell culture process parameters |
EP3338793A1 (en) | 2013-08-28 | 2018-06-27 | AbbVie Stemcentrx LLC | Novel sez6 modulators and methods of use |
US10035853B2 (en) | 2013-08-28 | 2018-07-31 | Abbvie Stemcentrx Llc | Site-specific antibody conjugation methods and compositions |
EP3892294A1 (en) | 2013-08-28 | 2021-10-13 | AbbVie Stemcentrx LLC | Site-specific antibody conjugation methods and compositions |
US10918714B2 (en) | 2013-09-06 | 2021-02-16 | Academia Sinica | Human iNKT cell activation using glycolipids with altered glycosyl groups |
US10111951B2 (en) | 2013-09-06 | 2018-10-30 | Academia Sinica | Human iNKT cell activation using glycolipids with altered glycosyl groups |
US10611794B2 (en) | 2013-09-25 | 2020-04-07 | Bioverativ Therapeutics Inc. | On-column viral inactivation methods |
EP3903599A1 (en) | 2013-09-25 | 2021-11-03 | Bioverativ Therapeutics Inc. | On-column viral inactivation methods |
US10450566B2 (en) | 2013-09-25 | 2019-10-22 | Cornell University | Compounds for inducing anti-tumor immunity and methods thereof |
US11578098B2 (en) | 2013-09-25 | 2023-02-14 | Bioverativ Therapeutics Inc. | On-column viral inactivation methods |
US10421965B2 (en) | 2013-09-25 | 2019-09-24 | Cornell University | Compounds for inducing anti-tumor immunity and methods thereof |
US9957506B2 (en) | 2013-09-25 | 2018-05-01 | Cornell University | Compounds for inducing anti-tumor immunity and methods thereof |
EP3757130A1 (en) | 2013-09-26 | 2020-12-30 | Costim Pharmaceuticals Inc. | Methods for treating hematologic cancers |
WO2015048520A1 (en) | 2013-09-27 | 2015-04-02 | Genentech, Inc. | Anti-pdl1 antibody formulations |
EP3626742A1 (en) | 2013-09-27 | 2020-03-25 | F. Hoffmann-La Roche AG | Anti-pdl1 antibody formulations |
US10875922B2 (en) | 2013-09-27 | 2020-12-29 | Genentech, Inc. | Anti-PDL1 antibody formulations |
WO2015057939A1 (en) | 2013-10-18 | 2015-04-23 | Biogen Idec Ma Inc. | Anti-s1p4 antibodies and uses thereof |
EP4331590A2 (en) | 2013-10-29 | 2024-03-06 | President and Fellows of Harvard College | Nuclear factor erythroid 2-like 2 (nrf2) for use in treatment of age-related macular degeneration |
EP3777980A1 (en) | 2013-10-29 | 2021-02-17 | President and Fellows of Harvard College | Methods and compositions for inhibiting oxidative stress |
WO2015066190A1 (en) | 2013-10-29 | 2015-05-07 | President And Fellows Of Harvard College | Methods and compositions for inhibting oxidative stress |
WO2015070068A1 (en) | 2013-11-07 | 2015-05-14 | Abbvie Inc. | Isolation and purification of antibodies |
US11384397B2 (en) | 2013-11-12 | 2022-07-12 | Population Bio, Inc. | Methods and compositions for diagnosing, prognosing, and treating endometriosis |
EP2891722A1 (en) | 2013-11-12 | 2015-07-08 | Population Diagnostics, Inc. | Methods and compositions for diagnosing, prognosing, and treating endometriosis |
US10174376B2 (en) | 2013-11-12 | 2019-01-08 | Population Bio, Inc. | Methods and compositions for diagnosing, prognosing, and treating endometriosis |
EP3511422A2 (en) | 2013-11-12 | 2019-07-17 | Population Bio, Inc. | Methods and compositions for diagnosing, prognosing, and treating endometriosis |
WO2015071759A1 (en) | 2013-11-15 | 2015-05-21 | Institut Pasteur | A molecular marker of plasmodium falciparum artemisinin resistance |
EP4026909A1 (en) | 2013-12-19 | 2022-07-13 | Novartis AG | Human mesothelin chimeric antigen receptors and uses thereof |
WO2015090230A1 (en) | 2013-12-19 | 2015-06-25 | Novartis Ag | Human mesothelin chimeric antigen receptors and uses thereof |
WO2015095809A1 (en) | 2013-12-20 | 2015-06-25 | Biogen Idec Ma Inc. | Use of perfusion seed cultures to improve biopharmaceutical fed-batch production capacity and product quality |
US11708411B2 (en) | 2013-12-20 | 2023-07-25 | Wake Forest University Health Sciences | Methods and compositions for increasing protective antibody levels induced by pneumococcal polysaccharide vaccines |
EP3722321A1 (en) | 2013-12-23 | 2020-10-14 | Institut Pasteur | Phospholipase for treatment of immunosuppression |
WO2015109180A2 (en) | 2014-01-16 | 2015-07-23 | Academia Sinica | Compositions and methods for treatment and detection of cancers |
US9982041B2 (en) | 2014-01-16 | 2018-05-29 | Academia Sinica | Compositions and methods for treatment and detection of cancers |
US10150818B2 (en) | 2014-01-16 | 2018-12-11 | Academia Sinica | Compositions and methods for treatment and detection of cancers |
US10179911B2 (en) | 2014-01-20 | 2019-01-15 | President And Fellows Of Harvard College | Negative selection and stringency modulation in continuous evolution systems |
EP3738981A1 (en) | 2014-01-24 | 2020-11-18 | NGM Biopharmaceuticals, Inc. | Antibodies binding beta klotho domain 2 and methods of use thereof |
EP3514179A1 (en) | 2014-01-24 | 2019-07-24 | Dana-Farber Cancer Institute, Inc. | Antibody molecules to pd-1 and uses thereof |
EP4324518A2 (en) | 2014-01-31 | 2024-02-21 | Novartis AG | Antibody molecules to tim-3 and uses thereof |
WO2015120075A2 (en) | 2014-02-04 | 2015-08-13 | Genentech, Inc. | Mutant smoothened and methods of using the same |
EP4047015A1 (en) | 2014-02-11 | 2022-08-24 | Visterra, Inc. | Antibody molecules to dengue virus and uses thereof |
WO2015122995A1 (en) | 2014-02-11 | 2015-08-20 | Visterra, Inc. | Antibody moleules to dengue virus and uses thereof |
US10308721B2 (en) | 2014-02-21 | 2019-06-04 | Abbvie Stemcentrx Llc | Anti-DLL3 antibodies and drug conjugates for use in melanoma |
EP3660050A1 (en) | 2014-03-14 | 2020-06-03 | Novartis AG | Antibody molecules to lag-3 and uses thereof |
WO2015138920A1 (en) | 2014-03-14 | 2015-09-17 | Novartis Ag | Antibody molecules to lag-3 and uses thereof |
US11124760B2 (en) | 2014-03-24 | 2021-09-21 | Biogen Ma Inc. | Methods for overcoming glutamine deprivation during mammalian cell culture |
US10119972B2 (en) | 2014-03-27 | 2018-11-06 | Academia Sinica | Reactive labelling compounds and uses thereof |
WO2015175340A1 (en) | 2014-05-13 | 2015-11-19 | Bavarian Nordic, Inc. | Combination therapy for treating cancer with a poxvirus expressing a tumor antigen and a monoclonal antibody against tim-3 |
US10023892B2 (en) | 2014-05-27 | 2018-07-17 | Academia Sinica | Compositions and methods relating to universal glycoforms for enhanced antibody efficacy |
US11319567B2 (en) | 2014-05-27 | 2022-05-03 | Academia Sinica | Fucosidase from bacteroides and methods using the same |
US10618973B2 (en) | 2014-05-27 | 2020-04-14 | Academia Sinica | Anti-HER2 glycoantibodies and uses thereof |
US10005847B2 (en) | 2014-05-27 | 2018-06-26 | Academia Sinica | Anti-HER2 glycoantibodies and uses thereof |
US11884739B2 (en) | 2014-05-27 | 2024-01-30 | Academia Sinica | Anti-CD20 glycoantibodies and uses thereof |
US10118969B2 (en) | 2014-05-27 | 2018-11-06 | Academia Sinica | Compositions and methods relating to universal glycoforms for enhanced antibody efficacy |
US11332523B2 (en) | 2014-05-28 | 2022-05-17 | Academia Sinica | Anti-TNF-alpha glycoantibodies and uses thereof |
WO2015187779A1 (en) | 2014-06-03 | 2015-12-10 | Xbiotech, Inc. | Compositions and methods for treating and preventing staphylococcus aureus infections |
EP3970747A2 (en) | 2014-06-03 | 2022-03-23 | XBiotech Inc. | Compositions and methods for treating and preventing staphylococcus aureus infections |
EP2960252A1 (en) | 2014-06-26 | 2015-12-30 | Institut Pasteur | Phospholipase for treatment of immunosuppression |
EP3722316A1 (en) | 2014-07-21 | 2020-10-14 | Novartis AG | Treatment of cancer using a cd33 chimeric antigen receptor |
EP3511413A1 (en) | 2014-07-25 | 2019-07-17 | Theravectys | Lentiviral vectors for regulated expression of a chimeric antigen receptor molecule |
WO2016025880A1 (en) | 2014-08-14 | 2016-02-18 | Novartis Ag | Treatment of cancer using gfr alpha-4 chimeric antigen receptor |
EP3712171A1 (en) | 2014-08-19 | 2020-09-23 | Novartis AG | Treatment of cancer using a cd123 chimeric antigen receptor |
US11549145B2 (en) | 2014-09-05 | 2023-01-10 | Population Bio, Inc. | Methods and compositions for inhibiting and treating neurological conditions |
US10724096B2 (en) | 2014-09-05 | 2020-07-28 | Population Bio, Inc. | Methods and compositions for inhibiting and treating neurological conditions |
US10533034B2 (en) | 2014-09-08 | 2020-01-14 | Academia Sinica | Human iNKT cell activation using glycolipids |
US9879042B2 (en) | 2014-09-08 | 2018-01-30 | Academia Sinica | Human iNKT cell activation using glycolipids |
EP3925622A1 (en) | 2014-09-13 | 2021-12-22 | Novartis AG | Combination therapies |
WO2016040892A1 (en) | 2014-09-13 | 2016-03-17 | Novartis Ag | Combination therapies |
WO2016040880A1 (en) | 2014-09-13 | 2016-03-17 | Novartis Ag | Combination therapies of alk inhibitors |
EP3659621A1 (en) | 2014-09-13 | 2020-06-03 | Novartis AG | Combination therapies for cancer |
US11370833B2 (en) | 2014-09-15 | 2022-06-28 | Genentech, Inc. | Antibody formulations |
WO2016042412A1 (en) | 2014-09-16 | 2016-03-24 | Symphogen A/S | Anti-met antibodies and compositions |
US10400037B2 (en) | 2014-09-30 | 2019-09-03 | Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts | Binding molecules, especially antibodies, binding to L1CAM (CD171) |
EP3662903A2 (en) | 2014-10-03 | 2020-06-10 | Novartis AG | Combination therapies |
WO2016054555A2 (en) | 2014-10-03 | 2016-04-07 | Novartis Ag | Combination therapies |
WO2016061142A1 (en) | 2014-10-14 | 2016-04-21 | Novartis Ag | Antibody molecules to pd-l1 and uses thereof |
EP4245376A2 (en) | 2014-10-14 | 2023-09-20 | Novartis AG | Antibody molecules to pd-l1 and uses thereof |
WO2016061424A1 (en) | 2014-10-17 | 2016-04-21 | Biogen Ma Inc. | Copper supplementation for control of glycosylation in mammalian cell culture process |
US10920208B2 (en) | 2014-10-22 | 2021-02-16 | President And Fellows Of Harvard College | Evolution of proteases |
US11760986B2 (en) | 2014-10-22 | 2023-09-19 | President And Fellows Of Harvard College | Evolution of proteases |
WO2016070152A1 (en) | 2014-10-31 | 2016-05-06 | Biogen Ma Inc. | Hypotaurine, gaba, beta-alanine, and choline for control of waste byproduct accumulation in mammalian cell culture process |
US10208120B2 (en) | 2014-11-05 | 2019-02-19 | Genentech, Inc. | Anti-FGFR2/3 antibodies and methods using same |
WO2016073685A1 (en) | 2014-11-05 | 2016-05-12 | Annexon, Inc. | Humanized anti-complement factor c1q antibodies and uses thereof |
EP4295911A2 (en) | 2014-11-05 | 2023-12-27 | Annexon, Inc. | Humanized anti-complement factor c1q antibodies and uses thereof |
EP3632931A1 (en) | 2014-11-07 | 2020-04-08 | Sesen Bio, Inc. | Improved il-6 antibodies |
US11142571B2 (en) | 2014-11-07 | 2021-10-12 | Sesen Bio, Inc. | IL-6 antibodies |
WO2016073894A1 (en) | 2014-11-07 | 2016-05-12 | Eleven Biotherapeutics, Inc. | Therapeutic agents with increased ocular retention |
EP4268843A2 (en) | 2014-11-07 | 2023-11-01 | F. Hoffmann-La Roche Ltd | Improved il-6 antibodies |
WO2016081835A2 (en) | 2014-11-21 | 2016-05-26 | University Of Maryland, Baltimore | Targeted structure-specific particulate delivery systems |
US10093733B2 (en) | 2014-12-11 | 2018-10-09 | Abbvie Inc. | LRP-8 binding dual variable domain immunoglobulin proteins |
WO2016100882A1 (en) | 2014-12-19 | 2016-06-23 | Novartis Ag | Combination therapies |
US10435467B2 (en) | 2015-01-08 | 2019-10-08 | Biogen Ma Inc. | LINGO-1 antagonists and uses for treatment of demyelinating disorders |
US9975965B2 (en) | 2015-01-16 | 2018-05-22 | Academia Sinica | Compositions and methods for treatment and detection of cancers |
US10495645B2 (en) | 2015-01-16 | 2019-12-03 | Academia Sinica | Cancer markers and methods of use thereof |
WO2016114819A1 (en) | 2015-01-16 | 2016-07-21 | Academia Sinica | Compositions and methods for treatment and detection of cancers |
WO2016118961A1 (en) | 2015-01-24 | 2016-07-28 | Academia Sinica | Cancer markers and methods of use thereof |
US10342858B2 (en) | 2015-01-24 | 2019-07-09 | Academia Sinica | Glycan conjugates and methods of use thereof |
WO2016123593A1 (en) | 2015-01-30 | 2016-08-04 | Academia Sinica | Compositions and methods relating to universal glycoforms for enhanced antibody efficacy |
WO2016126972A1 (en) | 2015-02-04 | 2016-08-11 | Genentech, Inc. | Mutant smoothened and methods of using the same |
WO2016141111A1 (en) | 2015-03-03 | 2016-09-09 | Xoma (Us) Llc | Treatment of post-prandial hyperinsulinemia and hypoglycemia after bariatric surgery |
US10711067B2 (en) | 2015-03-03 | 2020-07-14 | Xoma (Us) Llc | Treatment of post-prandial hyperinsulinemia and hypoglycemia after bariatric surgery |
EP3735982A1 (en) | 2015-03-10 | 2020-11-11 | The University of Massachusetts | Targeting gdf6 and bmp signaling for anti-melanoma therapy |
WO2016144917A1 (en) | 2015-03-10 | 2016-09-15 | University Of Massachusetts | Targeting gdf6 and bmp signaling for anti-melanoma therapy |
WO2016161410A2 (en) | 2015-04-03 | 2016-10-06 | Xoma Technology Ltd. | Treatment of cancer using inhibitors of tgf-beta and pd-1 |
EP3770171A1 (en) | 2015-04-03 | 2021-01-27 | XOMA Technology Ltd. | Treatment of cancer using inhibitors of tgf-beta and pd-1 |
US11685775B2 (en) | 2015-04-03 | 2023-06-27 | Xoma Technology Ltd. | Method of increasing the ratio of effector T cells to regulatory T cells in a tumor by administering to a subject a TGF-beta inhibitor and a PD-1 antibody |
US10167334B2 (en) | 2015-04-03 | 2019-01-01 | Xoma Technology Ltd. | Treatment of cancer using anti-TGF-BETA and PD-1 antibodies |
US10683347B2 (en) | 2015-04-03 | 2020-06-16 | Xoma Technology Ltd. | Treatment of cancer using anti-TGF-β and anti-PD-1 antibodies |
US11299729B2 (en) | 2015-04-17 | 2022-04-12 | President And Fellows Of Harvard College | Vector-based mutagenesis system |
WO2016170022A1 (en) | 2015-04-21 | 2016-10-27 | Institut Gustave Roussy | Therapeutic methods, products and compositions inhibiting znf555 |
EP3626744A1 (en) | 2015-05-29 | 2020-03-25 | AbbVie Inc. | Anti-cd40 antibodies and uses thereof |
EP4047022A1 (en) | 2015-05-29 | 2022-08-24 | AbbVie Inc. | Anti-cd40 antibodies and uses thereof |
US11208452B2 (en) | 2015-06-02 | 2021-12-28 | Novo Nordisk A/S | Insulins with polar recombinant extensions |
US9840554B2 (en) | 2015-06-15 | 2017-12-12 | Abbvie Inc. | Antibodies against platelet-derived growth factor (PDGF) |
US11905623B2 (en) | 2015-07-22 | 2024-02-20 | President And Fellows Of Harvard College | Evolution of site-specific recombinases |
US10392674B2 (en) | 2015-07-22 | 2019-08-27 | President And Fellows Of Harvard College | Evolution of site-specific recombinases |
US11104967B2 (en) | 2015-07-22 | 2021-08-31 | President And Fellows Of Harvard College | Evolution of site-specific recombinases |
US11524983B2 (en) | 2015-07-23 | 2022-12-13 | President And Fellows Of Harvard College | Evolution of Bt toxins |
EP3878465A1 (en) | 2015-07-29 | 2021-09-15 | Novartis AG | Combination therapies comprising antibody molecules to tim-3 |
WO2017019897A1 (en) | 2015-07-29 | 2017-02-02 | Novartis Ag | Combination therapies comprising antibody molecules to tim-3 |
EP3964528A1 (en) | 2015-07-29 | 2022-03-09 | Novartis AG | Combination therapies comprising antibody molecules to lag-3 |
WO2017019894A1 (en) | 2015-07-29 | 2017-02-02 | Novartis Ag | Combination therapies comprising antibody molecules to lag-3 |
US10612011B2 (en) | 2015-07-30 | 2020-04-07 | President And Fellows Of Harvard College | Evolution of TALENs |
US11078469B2 (en) | 2015-07-30 | 2021-08-03 | President And Fellows Of Harvard College | Evolution of TALENs |
US11913040B2 (en) | 2015-07-30 | 2024-02-27 | President And Fellows Of Harvard College | Evolution of TALENs |
US11312936B2 (en) | 2015-08-04 | 2022-04-26 | Regeneron Pharmaceuticals, Inc. | Taurine supplemented cell culture medium and methods of use |
US10927342B2 (en) | 2015-08-04 | 2021-02-23 | Regeneran Pharmaceuticals, Inc. | Taurine supplemented cell culture medium and methods of use |
US10253101B2 (en) | 2015-08-06 | 2019-04-09 | Xoma (Us) Llc | Antibody fragments against the insulin receptor and uses thereof to treat hypoglycemia |
WO2017040342A1 (en) | 2015-08-28 | 2017-03-09 | Genentech, Inc. | Anti-hypusine antibodies and uses thereof |
EP3932953A1 (en) | 2015-08-28 | 2022-01-05 | F. Hoffmann-La Roche AG | Anti-hypusine antibodies and uses thereof |
US10935544B2 (en) | 2015-09-04 | 2021-03-02 | Obi Pharma, Inc. | Glycan arrays and method of use |
WO2017049011A1 (en) | 2015-09-15 | 2017-03-23 | Scholar Rock, Inc. | Anti-pro/latent-myostatin antibodies and uses thereof |
EP3922645A1 (en) | 2015-09-15 | 2021-12-15 | Scholar Rock, Inc. | Anti-pro/latent-myostatin antibodies and uses thereof |
US10428145B2 (en) | 2015-09-29 | 2019-10-01 | Celgene Corporation | PD-1 binding proteins and methods of use thereof |
US11292825B2 (en) | 2015-10-01 | 2022-04-05 | Novo Nordisk A/S | Protein conjugates |
WO2017066561A2 (en) | 2015-10-16 | 2017-04-20 | President And Fellows Of Harvard College | Regulatory t cell pd-1 modulation for regulating t cell effector immune responses |
WO2017075329A2 (en) | 2015-10-29 | 2017-05-04 | Dana-Farber Cancer Institute, Inc. | Methods for identification, assessment, prevention, and treatment of metabolic disorders using pm20d1 and n-lipidated amino acids |
WO2017077275A1 (en) * | 2015-11-02 | 2017-05-11 | Imperial Innovations Limited | Phagemid vector |
US11603540B2 (en) | 2015-11-02 | 2023-03-14 | Imperial College Innovations Limited | Phagemid vector |
WO2017083515A2 (en) | 2015-11-10 | 2017-05-18 | Visterra, Inc. | Antibody molecule-drug conjugates and uses thereof |
EP4285923A2 (en) | 2015-11-25 | 2023-12-06 | Visterra, Inc. | Antibody molecules to april and uses thereof |
WO2017091683A1 (en) | 2015-11-25 | 2017-06-01 | Visterra, Inc. | Antibody molecules to april and uses thereof |
WO2017106656A1 (en) | 2015-12-17 | 2017-06-22 | Novartis Ag | Antibody molecules to pd-1 and uses thereof |
WO2017106810A2 (en) | 2015-12-17 | 2017-06-22 | Novartis Ag | Combination of c-met inhibitor with antibody molecule to pd-1 and uses thereof |
US10525137B2 (en) | 2015-12-30 | 2020-01-07 | Genentech, Inc. | Formulations with reduced degradation of polysorbate |
WO2017117304A1 (en) | 2015-12-30 | 2017-07-06 | Genentech, Inc. | Use of tryptophan derivatives for protein formulations |
WO2017117311A1 (en) | 2015-12-30 | 2017-07-06 | Genentech, Inc. | Formulations with reduced degradation of polysorbate |
US10933141B2 (en) | 2015-12-30 | 2021-03-02 | Genentech, Inc. | Formulations with reduced degradation of polysorbate |
WO2017120523A2 (en) | 2016-01-08 | 2017-07-13 | Scholar Rock, Inc. | Anti-pro/latent myostatin antibodies and methods of use thereof |
WO2017136558A1 (en) | 2016-02-04 | 2017-08-10 | Curis, Inc. | Mutant smoothened and methods of using the same |
US11725247B2 (en) | 2016-02-29 | 2023-08-15 | Foundation Medicine, Inc. | Methods of treating cancer |
US10336784B2 (en) | 2016-03-08 | 2019-07-02 | Academia Sinica | Methods for modular synthesis of N-glycans and arrays thereof |
EP4169942A1 (en) | 2016-03-11 | 2023-04-26 | Scholar Rock, Inc. | Tgfbeta1-binding immunoglobulins and use thereof |
WO2017156500A1 (en) | 2016-03-11 | 2017-09-14 | Scholar Rock, Inc. | Tgfb1-binding immunoglobulins and use thereof |
WO2017160599A1 (en) | 2016-03-14 | 2017-09-21 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Use of cd300b antagonists to treat sepsis and septic shock |
WO2017158436A1 (en) | 2016-03-17 | 2017-09-21 | Oslo Universitetssykehus Hf | Fusion proteins targeting tumour associated macrophages for treating cancer |
WO2017165464A1 (en) | 2016-03-21 | 2017-09-28 | Elstar Therapeutics, Inc. | Multispecific and multifunctional molecules and uses thereof |
WO2017165736A1 (en) | 2016-03-25 | 2017-09-28 | Visterra, Inc. | Formulation of antibody molecules to dengue virus |
US11833223B2 (en) | 2016-03-29 | 2023-12-05 | Obi Pharma, Inc. | Antibodies, pharmaceutical compositions and methods |
US11041017B2 (en) | 2016-03-29 | 2021-06-22 | Obi Pharma, Inc. | Antibodies, pharmaceutical compositions and methods |
US10980894B2 (en) | 2016-03-29 | 2021-04-20 | Obi Pharma, Inc. | Antibodies, pharmaceutical compositions and methods |
WO2017177199A2 (en) | 2016-04-08 | 2017-10-12 | Iti Health, Inc. | Plectin-1 binding antibodies and uses thereof |
WO2017181098A2 (en) | 2016-04-15 | 2017-10-19 | Visterra, Inc. | Antibody molecules to zika virus and uses thereof |
US11583577B2 (en) | 2016-04-22 | 2023-02-21 | Obi Pharma, Inc. | Cancer immunotherapy by immune activation or immune modulation via Globo series antigens |
EP3992632A1 (en) | 2016-06-27 | 2022-05-04 | Juno Therapeutics, Inc. | Mhc-e restricted epitopes, binding molecules and related methods and uses |
WO2018005556A1 (en) | 2016-06-27 | 2018-01-04 | Juno Therapeutics, Inc. | Mhc-e restricted epitopes, binding molecules and related methods and uses |
WO2018005559A1 (en) | 2016-06-27 | 2018-01-04 | Juno Therapeutics, Inc. | Method of identifying peptide epitopes, molecules that bind such epitopes and related uses |
WO2018013714A1 (en) | 2016-07-13 | 2018-01-18 | Biogen Ma Inc. | Dosage regimens of lingo-1 antagonists and uses for treatment of demyelinating disorders |
WO2018013918A2 (en) | 2016-07-15 | 2018-01-18 | Novartis Ag | Treatment and prevention of cytokine release syndrome using a chimeric antigen receptor in combination with a kinase inhibitor |
WO2018022479A1 (en) | 2016-07-25 | 2018-02-01 | Biogen Ma Inc. | Anti-hspa5 (grp78) antibodies and uses thereof |
US11642400B2 (en) | 2016-07-27 | 2023-05-09 | Obi Pharma, Inc. | Immunogenic/therapeutic glycan compositions and uses thereof |
US11643456B2 (en) | 2016-07-29 | 2023-05-09 | Obi Pharma, Inc. | Human antibodies, pharmaceutical compositions and methods |
WO2018026748A1 (en) | 2016-08-01 | 2018-02-08 | Xoma (Us) Llc | Parathyroid hormone receptor 1 (pth1r) antibodies and uses thereof |
US10519250B2 (en) | 2016-08-01 | 2019-12-31 | Xoma (Us) Llc | Parathyroid hormone receptor 1 (PTH1R) antibodies and uses thereof |
US11787876B2 (en) | 2016-08-01 | 2023-10-17 | Xoma (Us) Llc | Parathyroid hormone receptor 1 (PTH1R) antibodies and uses thereof |
WO2018052556A1 (en) | 2016-08-02 | 2018-03-22 | Visterra, Inc. | Engineered polypeptides and uses thereof |
US11649285B2 (en) | 2016-08-03 | 2023-05-16 | Bio-Techne Corporation | Identification of VSIG3/VISTA as a novel immune checkpoint and use thereof for immunotherapy |
US10538592B2 (en) | 2016-08-22 | 2020-01-21 | Cho Pharma, Inc. | Antibodies, binding fragments, and methods of use |
US10766958B2 (en) | 2016-09-19 | 2020-09-08 | Celgene Corporation | Methods of treating vitiligo using PD-1 binding antibodies |
US10751414B2 (en) | 2016-09-19 | 2020-08-25 | Celgene Corporation | Methods of treating psoriasis using PD-1 binding antibodies |
US11673971B2 (en) | 2016-09-23 | 2023-06-13 | Marengo Therapeutics, Inc. | Multispecific antibody molecules comprising lambda and kappa light chains |
WO2018057955A1 (en) | 2016-09-23 | 2018-03-29 | Elstar Therapeutics, Inc. | Multispecific antibody molecules comprising lambda and kappa light chains |
US10858428B2 (en) | 2016-09-28 | 2020-12-08 | Xoma (Us) Llc | Antibodies that bind interleukin-2 and uses thereof |
WO2018064255A2 (en) | 2016-09-28 | 2018-04-05 | Xoma (Us) Llc | Antibodies that bind interleukin-2 and uses thereof |
WO2018067468A1 (en) | 2016-10-03 | 2018-04-12 | Abbott Laboratories | Improved methods of assessing uch-l1 status in patient samples |
WO2018067474A1 (en) | 2016-10-03 | 2018-04-12 | Abbott Laboratories | Improved methods of assessing gfap status in patient samples |
WO2018067992A1 (en) | 2016-10-07 | 2018-04-12 | Novartis Ag | Chimeric antigen receptors for the treatment of cancer |
WO2018071576A1 (en) | 2016-10-14 | 2018-04-19 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Treatment of tumors by inhibition of cd300f |
US11000601B2 (en) | 2016-11-21 | 2021-05-11 | Obi Pharma, Inc. | Conjugated biological molecules, pharmaceutical compositions and methods |
WO2018119402A1 (en) | 2016-12-23 | 2018-06-28 | Visterra, Inc. | Binding polypeptides and methods of making the same |
WO2018129395A1 (en) | 2017-01-06 | 2018-07-12 | Scholar Rock, Inc. | Methods for treating metabolic diseases by inhibiting myostatin activation |
WO2018129329A1 (en) | 2017-01-06 | 2018-07-12 | Scholar Rock, Inc. | ISOFORM-SPECIFIC, CONTEXT-PERMISSIVE TGFβ1 INHIBITORS AND USE THEREOF |
EP4218817A2 (en) | 2017-01-06 | 2023-08-02 | Scholar Rock, Inc. | Methods for treating metabolic diseases by inhibiting myostatin activation |
WO2018130661A1 (en) | 2017-01-13 | 2018-07-19 | Academia Sinica | Reloadable hydrogel system for treating brain conditions |
WO2018130660A1 (en) | 2017-01-13 | 2018-07-19 | Academia Sinica | Reloadable hydrogel system for treating myocardial infarction |
WO2018136626A1 (en) | 2017-01-18 | 2018-07-26 | Visterra, Inc. | Antibody molecule-drug conjugates and uses thereof |
WO2018136553A1 (en) | 2017-01-18 | 2018-07-26 | Genentech, Inc. | Idiotypic antibodies against anti-pd-l1 antibodies and uses thereof |
US11279762B2 (en) | 2017-01-18 | 2022-03-22 | Genentech, Inc. | Idiotypic antibodies against anti-PD-L1 antibodies and uses thereof |
US10941448B1 (en) | 2017-02-03 | 2021-03-09 | The Universite Paris-Saclay | Methods for assessing risk of developing a viral disease using a genetic test |
US10544463B2 (en) | 2017-02-03 | 2020-01-28 | Pml Screening, Llc | Methods for assessing risk of developing a viral disease using a genetic test |
US10563264B2 (en) | 2017-02-03 | 2020-02-18 | Pml Screening, Llc | Methods for assessing risk of developing a viral disease using a genetic test |
US11913073B2 (en) | 2017-02-03 | 2024-02-27 | Pml Screening, Llc | Methods for assessing risk of developing a viral disease using a genetic test |
US10240205B2 (en) | 2017-02-03 | 2019-03-26 | Population Bio, Inc. | Methods for assessing risk of developing a viral disease using a genetic test |
US11623945B2 (en) | 2017-02-06 | 2023-04-11 | The United States Of America, As Represented By The Secretary Of Agriculture | Immunostimulating compositions and uses therefore |
WO2018151820A1 (en) | 2017-02-16 | 2018-08-23 | Elstar Therapeutics, Inc. | Multifunctional molecules comprising a trimeric ligand and uses thereof |
WO2018158719A1 (en) | 2017-03-02 | 2018-09-07 | Novartis Ag | Engineered heterodimeric proteins |
WO2018175942A1 (en) | 2017-03-23 | 2018-09-27 | Abbott Laboratories | Methods for aiding in the diagnosis and determination of the extent of traumatic brain injury in a human subject using the early biomarker ubiquitin carboxy-terminal hydrolase l1 |
WO2018176019A1 (en) | 2017-03-24 | 2018-09-27 | The Regents Of The University Of California | Proteoglycan irregularities in abnormal fibroblasts and therapies based therefrom |
WO2018187227A1 (en) | 2017-04-03 | 2018-10-11 | Concologie, Inc. | Methods for treating cancer using ps-targeting antibodies with immuno-oncology agents |
US11471537B2 (en) | 2017-04-05 | 2022-10-18 | Novo Nordisk A/S | Oligomer extended insulin-Fc conjugates |
WO2018189611A1 (en) | 2017-04-12 | 2018-10-18 | Pfizer Inc. | Antibodies having conditional affinity and methods of use thereof |
WO2018191531A1 (en) | 2017-04-15 | 2018-10-18 | Abbott Laboratories | Methods for aiding in the hyperacute diagnosis and determination of traumatic brain injury in a human subject using early biomarkers |
WO2018195283A1 (en) | 2017-04-19 | 2018-10-25 | Elstar Therapeutics, Inc. | Multispecific molecules and uses thereof |
US11820792B2 (en) | 2017-04-24 | 2023-11-21 | Imperial College Innovations Limited | Cancer treatment |
WO2018197859A1 (en) * | 2017-04-24 | 2018-11-01 | Imperial Innovations Limited | Cancer treatment |
CN110546253A (en) * | 2017-04-24 | 2019-12-06 | 帝国创新有限公司 | cancer treatment |
WO2018201047A1 (en) | 2017-04-28 | 2018-11-01 | Elstar Therapeutics, Inc. | Multispecific molecules comprising a non-immunoglobulin heterodimerization domain and uses thereof |
WO2018200823A1 (en) | 2017-04-28 | 2018-11-01 | Abbott Laboratories | Methods for aiding in the hyperacute diagnosis and determination of traumatic brain injury using early biomarkers on at least two samples from the same human subject |
EP4328241A2 (en) | 2017-04-28 | 2024-02-28 | Marengo Therapeutics, Inc. | Multispecific molecules comprising a non-immunoglobulin heterodimerization domain and uses thereof |
US10865238B1 (en) | 2017-05-05 | 2020-12-15 | Duke University | Complement factor H antibodies |
WO2018215535A1 (en) | 2017-05-23 | 2018-11-29 | Helmholtz Zentrum München - Deutsches Forschungszentrum für Gesundheit und Umwelt (GmbH) | Novel cd73 antibody, preparation and uses thereof |
WO2018218169A1 (en) | 2017-05-25 | 2018-11-29 | Abbott Laboratories | Methods for aiding in the determination of whether to perform imaging on a human subject who has sustained or may have sustained an injury to the head using early biomarkers |
WO2018222783A1 (en) | 2017-05-30 | 2018-12-06 | Abbott Laboratories | Methods for aiding in diagnosing and evaluating a mild traumatic brain injury in a human subject using cardiac troponin i and early biomarkers |
WO2018222784A1 (en) | 2017-05-30 | 2018-12-06 | Abbott Laboratories | Methods for aiding in diagnosing and evaluating a mild traumatic brain injury in a human subject using cardiac troponin i |
WO2018222901A1 (en) | 2017-05-31 | 2018-12-06 | Elstar Therapeutics, Inc. | Multispecific molecules that bind to myeloproliferative leukemia (mpl) protein and uses thereof |
WO2018226336A1 (en) | 2017-06-09 | 2018-12-13 | Providence Health & Services - Oregon | Utilization of cd39 and cd103 for identification of human tumor reactive cells for treatment of cancer |
WO2018237173A1 (en) | 2017-06-22 | 2018-12-27 | Novartis Ag | Antibody molecules to cd73 and uses thereof |
US11897958B2 (en) | 2017-06-26 | 2024-02-13 | Bio-Techne Corporation | Hybridoma clones, monoclonal antibodies to VSIG-4, and methods of making and using |
US10752689B2 (en) | 2017-06-26 | 2020-08-25 | Bio-Techne Corporation | Hybridoma clones, monoclonal antibodies to VSIG-4, and methods of making and using |
WO2019006007A1 (en) | 2017-06-27 | 2019-01-03 | Novartis Ag | Dosage regimens for anti-tim-3 antibodies and uses thereof |
WO2019010131A1 (en) | 2017-07-03 | 2019-01-10 | Abbott Laboratories | Improved methods for measuring ubiquitin carboxy-terminal hydrolase l1 levels in blood |
US11447809B2 (en) | 2017-07-06 | 2022-09-20 | President And Fellows Of Harvard College | Evolution of tRNA synthetases |
US11802156B2 (en) | 2017-07-14 | 2023-10-31 | Pfizer Inc. | Antibodies to MAdCAM |
WO2019014572A1 (en) | 2017-07-14 | 2019-01-17 | Pfizer, Inc. | Antibodies to madcam |
WO2019016213A1 (en) | 2017-07-19 | 2019-01-24 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | ANTI- ISOASP7 AMYLOID β (Aβ) ANTIBODIES AND USES THEREOF |
US11703511B2 (en) | 2017-07-19 | 2023-07-18 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Anti-isoAsp7 amyloid β (Aβ) antibodies and uses thereof |
EP3431496A1 (en) | 2017-07-19 | 2019-01-23 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Anti- isoasp7 amyloid beta antibodies and uses thereof |
WO2019018730A1 (en) | 2017-07-20 | 2019-01-24 | Novartis Ag | Dosage regimens of anti-lag-3 antibodies and uses thereof |
WO2019023661A1 (en) | 2017-07-28 | 2019-01-31 | Scholar Rock, Inc. | Ltbp complex-specific inhibitors of tgf-beta 1 and uses thereof |
WO2019035938A1 (en) | 2017-08-16 | 2019-02-21 | Elstar Therapeutics, Inc. | Multispecific molecules that bind to bcma and uses thereof |
US11624130B2 (en) | 2017-09-18 | 2023-04-11 | President And Fellows Of Harvard College | Continuous evolution for stabilized proteins |
WO2019068733A1 (en) | 2017-10-02 | 2019-04-11 | Certest Biotec, S.L. | Antibodies and test devices for the detection of bacteria of the genus campylobacter |
WO2019070726A1 (en) | 2017-10-02 | 2019-04-11 | Visterra, Inc. | Antibody molecules to cd138 and uses thereof |
EP3461841A1 (en) | 2017-10-02 | 2019-04-03 | Certest Biotec, S.L. | Antibodies and test devices for the detection of bacteria of the genus campylobacter |
US11215618B2 (en) | 2017-10-04 | 2022-01-04 | Hesperix SA | Articles and methods directed to personalized therapy of cancer |
WO2019070161A2 (en) | 2017-10-04 | 2019-04-11 | Opko Pharmaceuticals, Llc | Articles and methods directed to personalized therapy of cancer |
WO2019077132A1 (en) | 2017-10-19 | 2019-04-25 | Debiopharm International S.A. | Combination product for the treatment of cancer |
WO2019077165A1 (en) | 2017-10-20 | 2019-04-25 | Institut Curie | Dap10/12 based cars adapted for rush |
WO2019099838A1 (en) | 2017-11-16 | 2019-05-23 | Novartis Ag | Combination therapies |
WO2019108755A1 (en) | 2017-11-30 | 2019-06-06 | Genentech, Inc. | Anti-pd-l1 antibodies and methods of using the same for detection of pd-l1 |
US11292843B2 (en) | 2017-11-30 | 2022-04-05 | Genentech, Inc. | Anti-PD-L1 antibodies and methods of using the same for detection of PD-L1 |
WO2019113464A1 (en) | 2017-12-08 | 2019-06-13 | Elstar Therapeutics, Inc. | Multispecific molecules and uses thereof |
WO2019112860A1 (en) | 2017-12-09 | 2019-06-13 | Abbott Laboratories | Methods for aiding in diagnosing and evaluating a traumatic brain injury in a human subject using a combination of gfap and uch-l1 |
WO2019113525A2 (en) | 2017-12-09 | 2019-06-13 | Abbott Laboratories | Methods for aiding in the diagnosis and evaluation of a subject who has sustained an orthopedic injury and that has or may have sustained an injury to the head, such as mild traumatic brain injury (tbi), using glial fibrillary acidic protein (gfap) and/or ubiquitin carboxy-terminal hydrolase l1 (uch-l1) |
WO2019152810A1 (en) | 2018-02-02 | 2019-08-08 | Bio-Techne Corporation | Compounds that modulate the interaction of vista and vsig3 and methods of making and using |
US11787857B2 (en) | 2018-02-02 | 2023-10-17 | Bio-Techne Corporation | Compounds that modulate the interaction of VISTA and VSIG3 and methods of making and using |
US10982002B2 (en) | 2018-03-12 | 2021-04-20 | Zoetis Services Llc | Anti-NGF antibodies and methods thereof |
WO2019178362A1 (en) | 2018-03-14 | 2019-09-19 | Elstar Therapeutics, Inc. | Multifunctional molecules that bind to calreticulin and uses thereof |
WO2019178364A2 (en) | 2018-03-14 | 2019-09-19 | Elstar Therapeutics, Inc. | Multifunctional molecules and uses thereof |
WO2019180272A1 (en) | 2018-03-23 | 2019-09-26 | Fundación Instituto De Investigación Sanitaria De Santiago De Compostela | Anti-leptin affinity reagents for use in the treatment of obesity and other leptin-resistance associated diseases |
EP4253958A2 (en) | 2018-03-26 | 2023-10-04 | Glycanostics s.r.o. | Means and methods for glycoprofiling of a protein |
WO2019185515A1 (en) | 2018-03-26 | 2019-10-03 | Glycanostics S.R.O. | Means and methods for glycoprofiling of a protein |
WO2019200229A1 (en) | 2018-04-13 | 2019-10-17 | Novartis Ag | Dosage regimens for anti-pd-l1 antibodies and uses thereof |
WO2019229658A1 (en) | 2018-05-30 | 2019-12-05 | Novartis Ag | Entpd2 antibodies, combination therapies, and methods of using the antibodies and combination therapies |
US11913044B2 (en) | 2018-06-14 | 2024-02-27 | President And Fellows Of Harvard College | Evolution of cytidine deaminases |
WO2019246293A2 (en) | 2018-06-19 | 2019-12-26 | Atarga, Llc | Antibody molecules to complement component 5 and uses thereof |
US11203645B2 (en) | 2018-06-27 | 2021-12-21 | Obi Pharma, Inc. | Glycosynthase variants for glycoprotein engineering and methods of use |
DE202019005887U1 (en) | 2018-07-03 | 2023-06-14 | Marengo Therapeutics, Inc. | Anti-TCR antibody molecules and uses thereof |
WO2020010250A2 (en) | 2018-07-03 | 2020-01-09 | Elstar Therapeutics, Inc. | Anti-tcr antibody molecules and uses thereof |
US11845797B2 (en) | 2018-07-03 | 2023-12-19 | Marengo Therapeutics, Inc. | Anti-TCR antibody molecules and uses thereof |
WO2020008083A1 (en) | 2018-07-05 | 2020-01-09 | Consejo Superior De Investigaciones Científicas | Therapeutic target in chemokine receptors for the screening of compounds useful for the treatment of pathological processes involving chemokine signaling |
EP3677278A1 (en) | 2018-07-11 | 2020-07-08 | Scholar Rock, Inc. | Isoform selective tgfbeta1 inhibitors and use thereof |
WO2020014473A1 (en) | 2018-07-11 | 2020-01-16 | Scholar Rock, Inc. | TGFβ1 INHIBITORS AND USE THEREOF |
WO2020014460A1 (en) | 2018-07-11 | 2020-01-16 | Scholar Rock, Inc. | HIGH-AFFINITY, ISOFORM-SELECTIVE TGFβ1 INHIBITORS AND USE THEREOF |
EP4019046A1 (en) | 2018-07-11 | 2022-06-29 | Scholar Rock, Inc. | Isoform selective tgfbeta1 inhibitors and use thereof |
WO2020021465A1 (en) | 2018-07-25 | 2020-01-30 | Advanced Accelerator Applications (Italy) S.R.L. | Method of treatment of neuroendocrine tumors |
WO2020033485A1 (en) | 2018-08-08 | 2020-02-13 | Genentech, Inc. | Use of tryptophan derivatives and l-methionine for protein formulation |
US11913074B2 (en) | 2018-08-08 | 2024-02-27 | Pml Screening, Llc | Methods for assessing risk of developing a viral disease using a genetic test |
US10961585B2 (en) | 2018-08-08 | 2021-03-30 | Pml Screening, Llc | Methods for assessing risk of developing a viral of disease using a genetic test |
WO2020069372A1 (en) | 2018-09-27 | 2020-04-02 | Elstar Therapeutics, Inc. | Csf1r/ccr2 multispecific antibodies |
WO2020065594A1 (en) | 2018-09-28 | 2020-04-02 | Kyowa Kirin Co., Ltd. | Il-36 antibodies and uses thereof |
WO2020070303A1 (en) | 2018-10-05 | 2020-04-09 | Bavarian Nordic A/S | Combination therapy for treating cancer with an intravenous administration of a recombinant mva and an immune checkpoint antagonist or agonist |
WO2020079580A1 (en) | 2018-10-15 | 2020-04-23 | Novartis Ag | Trem2 stabilizing antibodies |
WO2020086736A1 (en) | 2018-10-23 | 2020-04-30 | Scholar Rock, Inc. | Rgmc-selective inhibitors and use thereof |
WO2020086408A1 (en) | 2018-10-26 | 2020-04-30 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | A high-yield perfusion-based transient gene expression bioprocess |
WO2020104531A1 (en) | 2018-11-20 | 2020-05-28 | Bavarian Nordic A/S | Therapy for treating cancer with an intratumoral and/or intravenous administration of a recombinant mva encoding 4-1bbl (cd137l) and/or cd40l |
WO2020128898A1 (en) | 2018-12-20 | 2020-06-25 | Novartis Ag | Pharmaceutical combinations |
WO2020128927A1 (en) | 2018-12-20 | 2020-06-25 | Kyowa Kirin Co., Ltd. | Fn14 antibodies and uses thereof |
EP3689905A2 (en) | 2019-01-30 | 2020-08-05 | Scholar Rock, Inc. | Ltbp complex-specific inhibitors of tgf-beta and uses thereof |
WO2020160291A2 (en) | 2019-01-30 | 2020-08-06 | Scholar Rock, Inc. | LTBP COMPLEX-SPECIFIC INHIBITORS OF TGFβ AND USES THEREOF |
US11738050B2 (en) | 2019-02-01 | 2023-08-29 | Regents Of The University Of Minnesota | Compounds binding to fibroblast activation protein alpha |
EP3693063A1 (en) | 2019-02-06 | 2020-08-12 | Diaccurate | Methods and compositions for treating cancer |
WO2020161165A1 (en) | 2019-02-06 | 2020-08-13 | Diaccurate | Methods and compositions for treating cancer |
EP3696191A1 (en) | 2019-02-14 | 2020-08-19 | Fundación Instituto de Investigación contra la Leucemia Josep Carreras (IJC) | Car t-cells for the treatment of cd1a-positive cancer |
WO2020165350A1 (en) | 2019-02-14 | 2020-08-20 | Fundación Instituo De Investigación Contra La Leucemia Josep Carreras (Ijc) | Car t-cells for the treatment of cd1a-positive cancer |
WO2020165868A1 (en) | 2019-02-15 | 2020-08-20 | Perkinelmer Cellular Technologies Germany Gmbh | Low-power microscope-objective pre-scan and high-power microscope-objective scan in x,y and z-direction for imaging objects such as cells using a microscope |
WO2020172605A1 (en) | 2019-02-21 | 2020-08-27 | Elstar Therapeutics, Inc. | Antibody molecules that bind to nkp30 and uses thereof |
WO2020172598A1 (en) | 2019-02-21 | 2020-08-27 | Elstar Therapeutics, Inc. | Multifunctional molecules that bind to t cells and uses thereof to treat autoimmune disorders |
WO2020172601A1 (en) | 2019-02-21 | 2020-08-27 | Elstar Therapeutics, Inc. | Multifunctional molecules that bind to calreticulin and uses thereof |
WO2020172596A1 (en) | 2019-02-21 | 2020-08-27 | Elstar Therapeutics, Inc. | Anti-tcr antibody molecules and thereof |
WO2020172571A1 (en) | 2019-02-21 | 2020-08-27 | Elstar Therapeutics, Inc. | Multifunctional molecules that bind to t cell related cancer cells and uses thereof |
WO2020205523A1 (en) | 2019-03-29 | 2020-10-08 | Atarga, Llc | Anti fgf23 antibody |
WO2020213724A1 (en) | 2019-04-19 | 2020-10-22 | 中外製薬株式会社 | Chimeric receptor recognizing modification site of antibody |
WO2020257289A2 (en) | 2019-06-17 | 2020-12-24 | Visterra, Inc. | Humanized antibody molecules to cd138 and uses thereof |
WO2021010326A1 (en) | 2019-07-12 | 2021-01-21 | 中外製薬株式会社 | Anti-mutation type fgfr3 antibody and use therefor |
WO2021021606A1 (en) | 2019-07-26 | 2021-02-04 | Visterra, Inc. | Interleukin-2 agents and uses thereof |
WO2021023721A1 (en) | 2019-08-02 | 2021-02-11 | Fundacio Clinic Per A La Recerca Biomedica | Car t-cells against bcma for the treatment of multiple myeloma |
EP4272837A2 (en) | 2019-08-02 | 2023-11-08 | Fundacio de Recerca Clinic Barcelona-Institut d'Investigacions Biomèdiques August Pi I Sunyer | Car t-cells against bcma for the treatment of multiple myeloma |
WO2021023860A1 (en) | 2019-08-07 | 2021-02-11 | Db Biotech, As | Improved horseradish peroxidase polypeptides |
WO2021044009A1 (en) | 2019-09-04 | 2021-03-11 | Deutsches Zentrum Für Neurodegenerative Erkrankungen E.V. (Dzne) | Herv inhibitors for use in treating tauopathies |
WO2021053559A1 (en) | 2019-09-18 | 2021-03-25 | Novartis Ag | Entpd2 antibodies, combination therapies, and methods of using the antibodies and combination therapies |
WO2021053560A1 (en) | 2019-09-18 | 2021-03-25 | Novartis Ag | Combination therapy with entpd2 and cd73 antibodies |
WO2021079195A1 (en) | 2019-10-21 | 2021-04-29 | Novartis Ag | Tim-3 inhibitors and uses thereof |
WO2021079188A1 (en) | 2019-10-21 | 2021-04-29 | Novartis Ag | Combination therapies with venetoclax and tim-3 inhibitors |
WO2021099586A1 (en) | 2019-11-20 | 2021-05-27 | Bavarian Nordic A/S | Recombinant mva viruses for intratumoral and/or intravenous administration for treating cancer |
WO2021123902A1 (en) | 2019-12-20 | 2021-06-24 | Novartis Ag | Combination of anti tim-3 antibody mbg453 and anti tgf-beta antibody nis793, with or without decitabine or the anti pd-1 antibody spartalizumab, for treating myelofibrosis and myelodysplastic syndrome |
WO2021123996A1 (en) | 2019-12-20 | 2021-06-24 | Novartis Ag | Uses of anti-tgf-beta antibodies and checkpoint inhibitors for the treatment of proliferative diseases |
WO2021138407A2 (en) | 2020-01-03 | 2021-07-08 | Marengo Therapeutics, Inc. | Multifunctional molecules that bind to cd33 and uses thereof |
WO2021142427A1 (en) | 2020-01-11 | 2021-07-15 | Scholar Rock, Inc. | TGFβ INHIBITORS AND USE THEREOF |
WO2021142448A2 (en) | 2020-01-11 | 2021-07-15 | Scholar Rock,Inc. | Tgf-beta inhibitors and use thereof |
WO2021146320A1 (en) | 2020-01-13 | 2021-07-22 | Visterra, Inc. | Antibody molecules to c5ar1 and uses thereof |
WO2021144657A1 (en) | 2020-01-17 | 2021-07-22 | Novartis Ag | Combination comprising a tim-3 inhibitor and a hypomethylating agent for use in treating myelodysplastic syndrome or chronic myelomonocytic leukemia |
WO2021159024A1 (en) | 2020-02-05 | 2021-08-12 | Larimar Therapeutics, Inc. | Tat peptide binding proteins and uses thereof |
WO2021180890A1 (en) | 2020-03-11 | 2021-09-16 | Fundació Institut De Recerca Contra La Leucèmia Josep Carreras | Cd22 targeting-moiety for the treatment of b-cell acute lymphoblastic leukemia (b-all) |
WO2021203024A1 (en) | 2020-04-03 | 2021-10-07 | Visterra, Inc. | Antibody molecule-drug conjugates and uses thereof |
WO2021211331A1 (en) | 2020-04-13 | 2021-10-21 | Abbott Point Of Care Inc. | METHODS, COMPLEXES AND KITS FOR DETECTING OR DETERMINING AN AMOUNT OF A ß-CORONAVIRUS ANTIBODY IN A SAMPLE |
WO2021217085A1 (en) | 2020-04-24 | 2021-10-28 | Marengo Therapeutics, Inc. | Multifunctional molecules that bind to t cell related cancer cells and uses thereof |
WO2021222333A1 (en) | 2020-04-30 | 2021-11-04 | Genentech, Inc. | Kras specific antibodies and uses thereof |
WO2021220215A1 (en) | 2020-05-01 | 2021-11-04 | Novartis Ag | Engineered immunoglobulins |
WO2021220218A1 (en) | 2020-05-01 | 2021-11-04 | Novartis Ag | Immunoglobulin variants |
WO2021239666A1 (en) | 2020-05-26 | 2021-12-02 | Diaccurate | Therapeutic methods |
WO2021247908A1 (en) | 2020-06-03 | 2021-12-09 | Bionecure Therapeutics, Inc. | Trophoblast cell-surface antigen-2 (trop-2) antibodies |
WO2021262999A1 (en) | 2020-06-24 | 2021-12-30 | Visterra, Inc. | Antibody molecules to april and uses thereof |
WO2022010797A2 (en) | 2020-07-07 | 2022-01-13 | Bionecure Therapeutics, Inc. | Novel maytansinoids as adc payloads and their use for the treatment of cancer |
WO2022026592A2 (en) | 2020-07-28 | 2022-02-03 | Celltas Bio, Inc. | Antibody molecules to coronavirus and uses thereof |
WO2022031804A1 (en) | 2020-08-04 | 2022-02-10 | Abbott Laboratories | Improved methods and kits for detecting sars-cov-2 protein in a sample |
WO2022046920A2 (en) | 2020-08-26 | 2022-03-03 | Marengo Therapeutics, Inc. | Multifunctional molecules that bind to calreticulin and uses thereof |
WO2022046922A2 (en) | 2020-08-26 | 2022-03-03 | Marengo Therapeutics, Inc. | Antibody molecules that bind to nkp30 and uses thereof |
WO2022047046A1 (en) | 2020-08-26 | 2022-03-03 | Marengo Therapeutics, Inc. | Methods of detecting trbc1 or trbc2 |
WO2022043558A1 (en) | 2020-08-31 | 2022-03-03 | Advanced Accelerator Applications International Sa | Method of treating psma-expressing cancers |
WO2022043557A1 (en) | 2020-08-31 | 2022-03-03 | Advanced Accelerator Applications International Sa | Method of treating psma-expressing cancers |
WO2022081718A1 (en) | 2020-10-14 | 2022-04-21 | Five Prime Therapeutics, Inc. | Anti-c-c chemokine receptor 8 (ccr8) antibodies and methods of use thereof |
WO2022115538A1 (en) | 2020-11-24 | 2022-06-02 | Bio-Techne Corporation | Anti-severe acute respiratory syndrome coronavirus antibodies |
WO2022119841A1 (en) | 2020-12-01 | 2022-06-09 | Abbott Laboratories | Use of one or more biomarkers to determine traumatic brain injury (tbi) in a subject having received a head computerized tomography scan that is negative for a tbi |
WO2022120224A1 (en) | 2020-12-04 | 2022-06-09 | Visterra, Inc. | Methods of using interleukin-2 agents |
WO2022133191A2 (en) | 2020-12-18 | 2022-06-23 | Kiniksa Pharmaceuticals, Ltd. | Protein compositions and methods for producing and using the same |
WO2022147147A1 (en) | 2020-12-30 | 2022-07-07 | Abbott Laboratories | Methods for determining sars-cov-2 antigen and anti-sars-cov-2 antibody in a sample |
WO2022147463A2 (en) | 2020-12-31 | 2022-07-07 | Alamar Biosciences, Inc. | Binder molecules with high affinity and/ or specificity and methods of making and use thereof |
WO2022159590A1 (en) | 2021-01-20 | 2022-07-28 | Visterra, Inc. | Interleukin-2 mutants and uses thereof |
WO2022162569A1 (en) | 2021-01-29 | 2022-08-04 | Novartis Ag | Dosage regimes for anti-cd73 and anti-entpd2 antibodies and uses thereof |
WO2022182872A2 (en) | 2021-02-24 | 2022-09-01 | Alladapt Immunotherapeutics, Inc. | Compositions and methods for identification of cross-reactive allergenic proteins and treatment of allergies |
WO2022187440A1 (en) | 2021-03-03 | 2022-09-09 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | La protien as a novel regulator of osteoclastogenesis |
WO2022195551A1 (en) | 2021-03-18 | 2022-09-22 | Novartis Ag | Biomarkers for cancer and methods of use thereof |
WO2022204581A2 (en) | 2021-03-26 | 2022-09-29 | Scholar Rock, Inc. | Tgf-beta inhibitors and use thereof |
WO2022215011A1 (en) | 2021-04-07 | 2022-10-13 | Novartis Ag | USES OF ANTI-TGFβ ANTIBODIES AND OTHER THERAPEUTIC AGENTS FOR THE TREATMENT OF PROLIFERATIVE DISEASES |
WO2022216993A2 (en) | 2021-04-08 | 2022-10-13 | Marengo Therapeutics, Inc. | Multifuntional molecules binding to tcr and uses thereof |
WO2022245920A1 (en) | 2021-05-18 | 2022-11-24 | Abbott Laboratories | Methods of evaluating brain injury in a pediatric subject |
WO2022256723A2 (en) | 2021-06-03 | 2022-12-08 | Scholar Rock, Inc. | Tgf-beta inhibitors and therapeutic use thereof |
WO2022261018A1 (en) | 2021-06-07 | 2022-12-15 | Providence Health & Services - Oregon | Cxcr5, pd-1, and icos expressing tumor reactive cd4 t cells and their use |
WO2022261183A2 (en) | 2021-06-08 | 2022-12-15 | Dana-Farber Cancer Institute, Inc. | Compositions and methods for treating and/or identifying an agent for treating intestinal cancers |
WO2022266034A1 (en) | 2021-06-14 | 2022-12-22 | Abbott Laboratories | Methods of diagnosing or aiding in diagnosis of brain injury caused by acoustic energy, electromagnetic energy, an over pressurization wave, and/or blast wind |
WO2022271867A1 (en) | 2021-06-23 | 2022-12-29 | Scholar Rock, Inc. | A myostatin pathway inhibitor in combination with a glp-1 pathway activator for use in treating metabolic disorders |
WO2023288267A1 (en) | 2021-07-14 | 2023-01-19 | 2Seventy Bio, Inc. | Engineered t cell receptors fused to binding domains from antibodies |
WO2023018803A1 (en) | 2021-08-10 | 2023-02-16 | Byomass Inc. | Anti-gdf15 antibodies, compositions and uses thereof |
WO2023025927A1 (en) | 2021-08-26 | 2023-03-02 | Glycanostics S.R.O | Glycoprotein biomarkers for diagnosing cancer |
WO2023034777A1 (en) | 2021-08-31 | 2023-03-09 | Abbott Laboratories | Methods and systems of diagnosing brain injury |
WO2023041565A1 (en) | 2021-09-14 | 2023-03-23 | Glycanostics S.R.O | Use of lectins to determine mammaglobin-a glycoforms in breast cancer |
WO2023044483A2 (en) | 2021-09-20 | 2023-03-23 | Voyager Therapeutics, Inc. | Compositions and methods for the treatment of her2 positive cancer |
WO2023044094A1 (en) | 2021-09-20 | 2023-03-23 | Alnylam Pharmaceuticals, Inc. | Inhibin subunit beta e (inhbe) modulator compositions and methods of use thereof |
WO2023056268A1 (en) | 2021-09-30 | 2023-04-06 | Abbott Laboratories | Methods and systems of diagnosing brain injury |
WO2023056069A1 (en) | 2021-09-30 | 2023-04-06 | Angiex, Inc. | Degrader-antibody conjugates and methods of using same |
WO2023069421A1 (en) | 2021-10-18 | 2023-04-27 | Byomass Inc. | Anti-activin a antibodies, compositions and uses thereof |
WO2023092004A1 (en) | 2021-11-17 | 2023-05-25 | Voyager Therapeutics, Inc. | Compositions and methods for the treatment of tau-related disorders |
WO2023097254A1 (en) | 2021-11-24 | 2023-06-01 | Visterra, Inc. | Engineered antibody molecules to cd138 and uses thereof |
WO2023097119A2 (en) | 2021-11-29 | 2023-06-01 | Dana-Farber Cancer Institute, Inc. | Methods and compositions to modulate riok2 |
WO2023102384A1 (en) | 2021-11-30 | 2023-06-08 | Abbott Laboratories | Use of one or more biomarkers to determine traumatic brain injury (tbi) in a subject having received a head computerized tomography scan that is negative for a tbi |
WO2023102463A1 (en) | 2021-12-01 | 2023-06-08 | Visterra, Inc. | Methods of using interleukin-2 agents |
WO2023114978A1 (en) | 2021-12-17 | 2023-06-22 | Abbott Laboratories | Systems and methods for determining uch-l1, gfap, and other biomarkers in blood samples |
WO2023122213A1 (en) | 2021-12-22 | 2023-06-29 | Byomass Inc. | Targeting gdf15-gfral pathway cross-reference to related applications |
WO2023118508A1 (en) | 2021-12-23 | 2023-06-29 | Bavarian Nordic A/S | Recombinant mva viruses for intraperitoneal administration for treating cancer |
WO2023129942A1 (en) | 2021-12-28 | 2023-07-06 | Abbott Laboratories | Use of biomarkers to determine sub-acute traumatic brain injury (tbi) in a subject having received a head computerized tomography (ct) scan that is negative for a tbi or no head ct scan |
WO2023147107A1 (en) | 2022-01-31 | 2023-08-03 | Byomass Inc. | Myeloproliferative conditions |
WO2023150652A1 (en) | 2022-02-04 | 2023-08-10 | Abbott Laboratories | Lateral flow methods, assays, and devices for detecting the presence or measuring the amount of ubiquitin carboxy-terminal hydrolase l1 and/or glial fibrillary acidic protein in a sample |
WO2023150778A1 (en) | 2022-02-07 | 2023-08-10 | Visterra, Inc. | Anti-idiotype antibody molecules and uses thereof |
WO2023212518A1 (en) | 2022-04-25 | 2023-11-02 | Visterra, Inc. | Antibody molecules to april and uses thereof |
WO2023220695A2 (en) | 2022-05-13 | 2023-11-16 | Voyager Therapeutics, Inc. | Compositions and methods for the treatment of her2 positive cancer |
WO2023239803A1 (en) | 2022-06-08 | 2023-12-14 | Angiex, Inc. | Anti-tm4sf1 antibody-drug conjugates comprising cleavable linkers and methods of using same |
EP4296279A1 (en) | 2022-06-23 | 2023-12-27 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Anti-transthyretin (ttr) binding proteins and uses thereof |
WO2023247312A1 (en) | 2022-06-23 | 2023-12-28 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Anti-transthyretin (ttr) binding proteins and uses thereof |
WO2024006876A1 (en) | 2022-06-29 | 2024-01-04 | Abbott Laboratories | Magnetic point-of-care systems and assays for determining gfap in biological samples |
WO2024013727A1 (en) | 2022-07-15 | 2024-01-18 | Janssen Biotech, Inc. | Material and methods for improved bioengineered pairing of antigen-binding variable regions |
WO2024030976A2 (en) | 2022-08-03 | 2024-02-08 | Voyager Therapeutics, Inc. | Compositions and methods for crossing the blood brain barrier |
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US20080038717A1 (en) | 2008-02-14 |
EP0564531A1 (en) | 1993-10-13 |
CA2405246A1 (en) | 1992-06-11 |
US20060115874A1 (en) | 2006-06-01 |
US5834598A (en) | 1998-11-10 |
DE69129154T2 (en) | 1998-08-20 |
US5821047A (en) | 1998-10-13 |
US5750373A (en) | 1998-05-12 |
DK0564531T3 (en) | 1998-09-28 |
ATE164395T1 (en) | 1998-04-15 |
US6040136A (en) | 2000-03-21 |
CA2095633A1 (en) | 1992-06-04 |
EP0564531B1 (en) | 1998-03-25 |
CA2095633C (en) | 2003-02-04 |
WO1992009690A3 (en) | 1992-12-10 |
DE69129154D1 (en) | 1998-04-30 |
ES2113940T3 (en) | 1998-05-16 |
US20100035236A1 (en) | 2010-02-11 |
GR3026468T3 (en) | 1998-06-30 |
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