RU2547596C2 - Полиспецифические антитела - Google Patents
Полиспецифические антитела Download PDFInfo
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- RU2547596C2 RU2547596C2 RU2011112324/10A RU2011112324A RU2547596C2 RU 2547596 C2 RU2547596 C2 RU 2547596C2 RU 2011112324/10 A RU2011112324/10 A RU 2011112324/10A RU 2011112324 A RU2011112324 A RU 2011112324A RU 2547596 C2 RU2547596 C2 RU 2547596C2
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- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
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- C—CHEMISTRY; METALLURGY
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- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
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- A61K39/3955—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against proteinaceous materials, e.g. enzymes, hormones, lymphokines
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- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/22—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against growth factors ; against growth regulators
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
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- C07K16/2863—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against receptors for growth factors, growth regulators
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- C—CHEMISTRY; METALLURGY
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- C07K—PEPTIDES
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- C07K2317/00—Immunoglobulins specific features
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
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- C07K2317/565—Complementarity determining region [CDR]
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- C—CHEMISTRY; METALLURGY
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- C07K—PEPTIDES
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- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
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- C07K2317/90—Immunoglobulins specific features characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin
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- Micro-Organisms Or Cultivation Processes Thereof (AREA)
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| US20050106667A1 (en) * | 2003-08-01 | 2005-05-19 | Genentech, Inc | Binding polypeptides with restricted diversity sequences |
| US7758859B2 (en) * | 2003-08-01 | 2010-07-20 | Genentech, Inc. | Anti-VEGF antibodies |
| DK2059533T3 (da) | 2006-08-30 | 2013-02-25 | Genentech Inc | Multispecifikke antistoffer |
| CN102143977B (zh) | 2008-09-03 | 2014-08-06 | 霍夫曼-拉罗奇有限公司 | 多特异性抗体 |
| US8268314B2 (en) | 2008-10-08 | 2012-09-18 | Hoffmann-La Roche Inc. | Bispecific anti-VEGF/anti-ANG-2 antibodies |
| AU2011257121A1 (en) | 2010-05-27 | 2013-01-10 | Genmab A/S | Monoclonal antibodies against HER2 |
| JP6082344B2 (ja) | 2010-05-27 | 2017-02-15 | ゲンマブ エー／エス | Ｈｅｒ２エピトープに対するモノクローナル抗体 |
| WO2012098113A1 (en) * | 2011-01-17 | 2012-07-26 | Novo Nordisk A/S | Il-21 ligands |
| US9527925B2 (en) | 2011-04-01 | 2016-12-27 | Boehringer Ingelheim International Gmbh | Bispecific binding molecules binding to VEGF and ANG2 |
| AU2012245116A1 (en) | 2011-04-20 | 2013-11-07 | Genmab A/S | Bispecific antibodies against HER2 and CD3 |
| KR20140057356A (ko) | 2011-08-31 | 2014-05-12 | 제넨테크, 인크. | 진단 마커 |
| KR101453516B1 (ko) | 2011-09-20 | 2014-10-24 | 가톨릭대학교 산학협력단 | 항-ｖｅｇｆ 항체를 포함하는 자가면역질환 예방 및 치료용 조성물 |
| WO2013055530A1 (en) | 2011-09-30 | 2013-04-18 | Genentech, Inc. | Diagnostic methylation markers of epithelial or mesenchymal phenotype and response to egfr kinase inhibitor in tumours or tumour cells |
| EP2862875B1 (en) | 2012-06-14 | 2023-09-06 | Chugai Seiyaku Kabushiki Kaisha | ANTIGEN-BINDING MOLECULE CONTAINING MODIFIED Fc REGION |
| RS62509B1 (sr) | 2012-07-13 | 2021-11-30 | Roche Glycart Ag | Bispecifična anti-vegf/anti-ang-2 antitela i njihova upotreba u lečenju očnih vaskularnih bolesti |
| WO2014134169A1 (en) * | 2013-02-26 | 2014-09-04 | Senex Biotechnology, Inc. | Inhibitors of cdk8/19 for use in treating estrogen receptor positive breast cancer |
| ES2989110T3 (es) * | 2013-11-11 | 2024-11-25 | Chugai Pharmaceutical Co Ltd | Molécula de unión a antígeno que contiene región variable de anticuerpo modificada |
| JP2015097496A (ja) * | 2013-11-19 | 2015-05-28 | 国立大学法人 東京大学 | Ｒｏｂｏ１に対する親和性を向上させた抗体及び高親和性抗体の分子設計方法 |
| WO2015119841A1 (en) * | 2014-02-05 | 2015-08-13 | Merck Sharp & Dohme Corp. | Role of il-23 and pd-1 in autoreactive immune response |
| GB201411420D0 (en) * | 2014-06-26 | 2014-08-13 | Ucb Biopharma Sprl | Antibody constructs |
| CA2955984A1 (en) | 2014-07-22 | 2016-01-28 | The University Of Notre Dame Du Lac | Molecular constructs and uses thereof |
| WO2016042684A1 (ja) * | 2014-09-16 | 2016-03-24 | 国立大学法人東京海洋大学 | 濃縮された生着能をもつ未分化生殖細胞を用いた生殖細胞系列への分化誘導方法 |
| KR102390359B1 (ko) | 2014-09-29 | 2022-04-22 | 삼성전자주식회사 | 폴리펩타이드, 이를 포함하는 항 VEGF 항체 및 항 c-Met/항 VEGF 이중 특이 항체 |
| TWI740809B (zh) * | 2014-11-11 | 2021-10-01 | 日商中外製藥股份有限公司 | 包含經改變之抗體可變區之抗原結合分子的資料庫 |
| CN107106682B (zh) | 2015-08-26 | 2021-05-25 | 比森医疗股份有限公司 | 多特异性抗体平台和相关方法 |
| IL257565B2 (en) | 2015-09-23 | 2024-08-01 | Genentech Inc | Optimized variants of anti-vegf antibodies |
| GB201521447D0 (en) | 2015-12-04 | 2016-01-20 | Ucb Biopharma Sprl | De novo antibody design |
| WO2017132457A1 (en) * | 2016-01-28 | 2017-08-03 | Janssen Biotech, Inc. | BISPECIFIC ANTI-TNF-α/IL-17A ANTIBODIES AND ANTI-TNF-α ANTIBODIES AND METHODS OF THEIR USE |
| WO2018224550A1 (en) * | 2017-06-07 | 2018-12-13 | Philogen S.P.A | Vascular endothelial growth factor/anti-fibronectin antibody fusion proteins |
| CN107602702A (zh) * | 2017-09-22 | 2018-01-19 | 生标（上海）医疗器械科技有限公司 | 一种同时靶向人p185和血管内皮生长因子的抗体及其应用 |
| EP3720963A4 (en) | 2017-12-05 | 2021-12-08 | Chugai Seiyaku Kabushiki Kaisha | ANTIGEN BINDING MOLECULE INCLUDING A VARIABLE REGION OF MODIFIED ANTIBODIES BINDING TO CD3 AND CD137 |
| AU2019315226B2 (en) | 2018-08-03 | 2025-09-18 | Chugai Seiyaku Kabushiki Kaisha | Antigen-binding molecule containing two antigen-binding domains that are linked to each other |
| CN110850068B (zh) * | 2018-08-21 | 2023-08-15 | 上海恒润达生生物科技股份有限公司 | 一种嵌合抗原受体亲和力检测方法 |
| WO2020067399A1 (en) | 2018-09-28 | 2020-04-02 | Chugai Seiyaku Kabushiki Kaisha | Antigen-binding molecule comprising altered antibody variable region |
| US12392777B2 (en) | 2019-04-02 | 2025-08-19 | National Research Council Of Canada | Antibody variants with pH-dependent antigen binding for selective targeting of solid tumors |
| IL296803A (en) | 2020-03-31 | 2022-11-01 | Chugai Pharmaceutical Co Ltd | Multispecific antigen binding molecules targeting dll3 and their uses |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002355074A (ja) * | 2001-01-24 | 2002-12-10 | Univ Tsukuba | 腸管出血性病原性大腸菌ｏ１５７：ｈ７に特異的な核酸分子およびポリペプチド並びにこれらの使用方法 |
| WO2008027236A2 (en) * | 2006-08-30 | 2008-03-06 | Genentech, Inc. | Multispecific antibodies |
Family Cites Families (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4816567A (en) | 1983-04-08 | 1989-03-28 | Genentech, Inc. | Recombinant immunoglobin preparations |
| IL85035A0 (en) | 1987-01-08 | 1988-06-30 | Int Genetic Eng | Polynucleotide molecule,a chimeric antibody with specificity for human b cell surface antigen,a process for the preparation and methods utilizing the same |
| GB8823869D0 (en) | 1988-10-12 | 1988-11-16 | Medical Res Council | Production of antibodies |
| ATE102631T1 (de) | 1988-11-11 | 1994-03-15 | Medical Res Council | Klonierung von immunglobulin sequenzen aus den variabelen domaenen. |
| US5175384A (en) | 1988-12-05 | 1992-12-29 | Genpharm International | Transgenic mice depleted in mature t-cells and methods for making transgenic mice |
| DE3920358A1 (de) | 1989-06-22 | 1991-01-17 | Behringwerke Ag | Bispezifische und oligospezifische, mono- und oligovalente antikoerperkonstrukte, ihre herstellung und verwendung |
| WO1996033735A1 (en) | 1995-04-27 | 1996-10-31 | Abgenix, Inc. | Human antibodies derived from immunized xenomice |
| CA2050918A1 (en) | 1990-01-12 | 1991-07-13 | Raju Kucherlapati | Generation of xenogeneic antibodies |
| US5545806A (en) | 1990-08-29 | 1996-08-13 | Genpharm International, Inc. | Ransgenic non-human animals for producing heterologous antibodies |
| DE69133476T2 (de) | 1990-08-29 | 2006-01-05 | GenPharm International, Inc., Palo Alto | Transgene Mäuse fähig zur Produktion heterologer Antikörper |
| US5625126A (en) | 1990-08-29 | 1997-04-29 | Genpharm International, Inc. | Transgenic non-human animals for producing heterologous antibodies |
| US5633425A (en) | 1990-08-29 | 1997-05-27 | Genpharm International, Inc. | Transgenic non-human animals capable of producing heterologous antibodies |
| US5661016A (en) | 1990-08-29 | 1997-08-26 | Genpharm International Inc. | Transgenic non-human animals capable of producing heterologous antibodies of various isotypes |
| US5582996A (en) | 1990-12-04 | 1996-12-10 | The Wistar Institute Of Anatomy & Biology | Bifunctional antibodies and method of preparing same |
| WO1992010209A1 (en) | 1990-12-04 | 1992-06-25 | The Wistar Institute Of Anatomy And Biology | Bifunctional antibodies and method of preparing same |
| AU675916B2 (en) | 1991-06-14 | 1997-02-27 | Genentech Inc. | Method for making humanized antibodies |
| EP0617706B1 (en) | 1991-11-25 | 2001-10-17 | Enzon, Inc. | Multivalent antigen-binding proteins |
| US5932448A (en) | 1991-11-29 | 1999-08-03 | Protein Design Labs., Inc. | Bispecific antibody heterodimers |
| CZ287296B6 (en) | 1992-01-23 | 2000-10-11 | Merck Patent Gmbh | Antibody construct and structural kit for selective preparation thereof |
| US5491074A (en) | 1993-04-01 | 1996-02-13 | Affymax Technologies Nv | Association peptides |
| US5641870A (en) | 1995-04-20 | 1997-06-24 | Genentech, Inc. | Low pH hydrophobic interaction chromatography for antibody purification |
| CA2219486A1 (en) | 1995-04-28 | 1996-10-31 | Abgenix, Inc. | Human antibodies derived from immunized xenomice |
| DK1500329T3 (da) | 1996-12-03 | 2012-07-09 | Amgen Fremont Inc | Humane antistoffer, der specifikt binder TNF-alfa |
| EP2386575A3 (en) | 2000-06-29 | 2011-11-30 | Abbott Laboratories | Dual specificity antibodies and methods of making and using |
| US20020025317A1 (en) | 2000-07-20 | 2002-02-28 | Schering Ag | Bispecific monoclonal antibodies to IL-12 and IL-18 |
| WO2004003019A2 (en) | 2002-06-28 | 2004-01-08 | Domantis Limited | Immunoglobin single variant antigen-binding domains and dual-specific constructs |
| US6833441B2 (en) | 2001-08-01 | 2004-12-21 | Abmaxis, Inc. | Compositions and methods for generating chimeric heteromultimers |
| WO2003018749A2 (en) | 2001-08-22 | 2003-03-06 | Shengfeng Li | Compositions and methods for generating antigen-binding units |
| EP1513879B1 (en) * | 2002-06-03 | 2018-08-22 | Genentech, Inc. | Synthetic antibody phage libraries |
| RS20181002A1 (sr) | 2003-05-30 | 2018-12-31 | Genentech Inc | Tretman sa anti-vegf antitelima |
| HRP20120376T1 (hr) | 2003-12-23 | 2012-05-31 | Genentech | Nova protutijela protiv il-13 i njihove upotrebe |
| US20050282233A1 (en) | 2004-03-05 | 2005-12-22 | Ludwig Institute For Cancer Research | Multivalent antibody materials and methods for VEGF/PDGF family of growth factors |
| KR20070041781A (ko) | 2004-08-11 | 2007-04-19 | 트루비온 파마슈티칼스, 인코포레이티드 | 결합 도메인 융합 단백질 |
| EP1968633B2 (en) | 2006-01-04 | 2017-11-01 | Institut National de la Santé et de la Recherche Medicale | Combination therapy using anti-egfr and anti-her2 antibodies |
| EA015992B1 (ru) | 2006-03-17 | 2012-01-30 | Байоджен Айдек Эмэй Инк. | Стабилизированное антитело и многовалентная антигенсвязывающая молекула на его основе, способы получения и использования вышеназванного стабилизированного антитела |
| WO2009068649A2 (en) | 2007-11-30 | 2009-06-04 | Glaxo Group Limited | Antigen-binding constructs |
| CN102143977B (zh) | 2008-09-03 | 2014-08-06 | 霍夫曼-拉罗奇有限公司 | 多特异性抗体 |
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Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002355074A (ja) * | 2001-01-24 | 2002-12-10 | Univ Tsukuba | 腸管出血性病原性大腸菌ｏ１５７：ｈ７に特異的な核酸分子およびポリペプチド並びにこれらの使用方法 |
| WO2008027236A2 (en) * | 2006-08-30 | 2008-03-06 | Genentech, Inc. | Multispecific antibodies |
Non-Patent Citations (1)
| Title |
|---|
| РОЙТ А. и др., Иммунология, Москва, "Мир", 2000, 592 с * |
Also Published As
| Publication number | Publication date |
|---|---|
| TWI487712B (zh) | 2015-06-11 |
| MX353984B (es) | 2017-11-27 |
| AU2009288167A1 (en) | 2010-03-11 |
| SG193851A1 (en) | 2013-10-30 |
| EP2324061A1 (en) | 2011-05-25 |
| EP2324061B1 (en) | 2017-04-12 |
| US9017686B2 (en) | 2015-04-28 |
| KR20110081812A (ko) | 2011-07-14 |
| PE20150222A1 (es) | 2015-03-02 |
| JP2012501648A (ja) | 2012-01-26 |
| RU2011112324A (ru) | 2012-10-10 |
| PE20110593A1 (es) | 2011-09-10 |
| JP5796831B2 (ja) | 2015-10-21 |
| IL211349A0 (en) | 2011-05-31 |
| US8193321B2 (en) | 2012-06-05 |
| PH12013502230A1 (en) | 2016-01-25 |
| KR101705911B1 (ko) | 2017-02-10 |
| AR073538A1 (es) | 2010-11-17 |
| US20150315290A1 (en) | 2015-11-05 |
| AU2009288167B2 (en) | 2015-10-22 |
| BRPI0918648A2 (pt) | 2019-09-03 |
| US9522960B2 (en) | 2016-12-20 |
| TW201011047A (en) | 2010-03-16 |
| MX2011002389A (es) | 2011-05-23 |
| US20100322946A1 (en) | 2010-12-23 |
| WO2010027981A1 (en) | 2010-03-11 |
| ES2628108T3 (es) | 2017-08-01 |
| ZA201101970B (en) | 2012-05-30 |
| CN102143977A (zh) | 2011-08-03 |
| CN102143977B (zh) | 2014-08-06 |
| CA2734905A1 (en) | 2010-03-11 |
| US20110142852A1 (en) | 2011-06-16 |
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