ES2651521T3 - Inhibidores proteicos de las rutas del complemento y de VEGF y métodos de uso de los mismos - Google Patents
Inhibidores proteicos de las rutas del complemento y de VEGF y métodos de uso de los mismos Download PDFInfo
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- ES2651521T3 ES2651521T3 ES12853600.0T ES12853600T ES2651521T3 ES 2651521 T3 ES2651521 T3 ES 2651521T3 ES 12853600 T ES12853600 T ES 12853600T ES 2651521 T3 ES2651521 T3 ES 2651521T3
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Families Citing this family (50)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110078831A (zh) | 2011-12-01 | 2019-08-02 | 圆祥生命科技股份有限公司 | 补体和vegf途径的蛋白质抑制剂及其使用方法 |
| CN104721820A (zh) * | 2013-12-24 | 2015-06-24 | 信达生物制药(苏州)有限公司 | 双特异性单克隆抗体在治疗葡萄膜炎中的用途 |
| LT3110434T (lt) * | 2014-02-24 | 2018-12-27 | Takeda Gmbh | Sulieti uti baltymai |
| CN106459218B (zh) * | 2014-03-24 | 2021-03-02 | 宜明昂科生物医药技术(上海)有限公司 | 新的重组双功能融合蛋白、其制剂和用途 |
| US10155983B2 (en) | 2014-03-31 | 2018-12-18 | Machaon Diagnostics, Inc. | Method of diagnosis of complement-mediated thrombotic microangiopathies |
| US9840553B2 (en) | 2014-06-28 | 2017-12-12 | Kodiak Sciences Inc. | Dual PDGF/VEGF antagonists |
| CN105327346B (zh) * | 2014-08-07 | 2019-10-18 | 信达生物制药(苏州)有限公司 | 一种单克隆抗体在治疗银屑病中的应用 |
| CN104940926B (zh) | 2014-09-25 | 2017-09-22 | 信达生物制药(苏州)有限公司 | 重组融合蛋白制剂 |
| CN105435222B (zh) | 2014-09-25 | 2018-05-29 | 信达生物制药(苏州)有限公司 | 重组融合蛋白制剂 |
| CN106084062B (zh) * | 2015-04-28 | 2021-04-02 | 荣昌生物制药(烟台)有限公司 | 桥连的双特异性融合蛋白 |
| WO2017001990A1 (en) | 2015-06-28 | 2017-01-05 | Allgenesis Biotherapeutics Inc. | Fusion proteins for inhibiting angiogenesis |
| EP3377101A4 (en) * | 2015-11-19 | 2019-08-07 | Zhuhai Tairuishang Biopharm Ltd. | VEGF BINDING METHODS AND COMPOSITIONS |
| CN106890313A (zh) * | 2015-12-18 | 2017-06-27 | 信达生物制药(苏州)有限公司 | 用于治疗病理性近视的药物 |
| WO2017117464A1 (en) | 2015-12-30 | 2017-07-06 | Kodiak Sciences Inc. | Antibodies and conjugates thereof |
| WO2017114401A1 (zh) * | 2015-12-31 | 2017-07-06 | 江苏匡亚生物医药科技有限公司 | 具有补体调节活性的重组补体因子h-免疫球蛋白融合蛋白及其制备方法与应用 |
| KR101685532B1 (ko) * | 2016-04-26 | 2016-12-13 | 한국프라임제약주식회사 | 혈관내피성장인자 수용체 융합단백질 |
| EA037848B1 (ru) * | 2016-07-14 | 2021-05-27 | Общество С Ограниченной Ответственностью "Биохимический Агент" | Гибридный белок, полинуклеотид, генетическая конструкция, продуцент, препарат для регенерации хряща (варианты) |
| CA3026892A1 (en) * | 2017-05-10 | 2018-11-15 | Wellstat Immunotherapeutics, Llc | Enveloped virus resistant to complement inactivation for the treatment of cancer |
| 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 |
| GB201800620D0 (en) * | 2018-01-15 | 2018-02-28 | Univ Manchester | C3b Binding Polypeptide |
| BR112020017872A2 (pt) | 2018-03-02 | 2020-12-22 | Kodiak Sciences Inc. | Anticorpos de il-6 e construtos de fusão e conjugados dos mesmos |
| PT3793586T (pt) * | 2018-05-16 | 2024-07-10 | Csl Ltd | Variantes do receptor solúvel do complemento de tipo 1 e sua utilização |
| WO2020037309A1 (en) * | 2018-08-17 | 2020-02-20 | Trican Biotechnology Co., Ltd. | Anti-angiogenesis fusion protein and uses thereof |
| EP3863657A4 (en) * | 2018-10-12 | 2022-07-20 | Trican Biotechnology Co., Ltd | BIFUNCTIONAL FUSION PROTEINS AND USES THEREOF |
| GB2583560A (en) | 2018-12-11 | 2020-11-04 | Admirx Inc | Fusion protein constructs for complement associated disease |
| CN111378044B (zh) * | 2018-12-28 | 2022-07-15 | 长春金赛药业有限责任公司 | 抗体融合蛋白、制备方法及其应用 |
| CN111423512B (zh) * | 2019-01-10 | 2024-01-05 | 北京比洋生物技术有限公司 | 阻断血管内皮细胞生长且活化t细胞的多靶向融合蛋白和包含其的药物组合物 |
| WO2020213004A1 (en) * | 2019-04-13 | 2020-10-22 | National Centre For Cell Science | Daf-mcp chimeric proteins, process to manufacture the same and use of the chimeric protein for treating pathological conditions involving the complement system |
| WO2021072265A1 (en) | 2019-10-10 | 2021-04-15 | Kodiak Sciences Inc. | Methods of treating an eye disorder |
| WO2021076991A1 (en) * | 2019-10-17 | 2021-04-22 | Annexon, Inc. | Compositions and methods for treating blood disorders |
| CN114867489A (zh) * | 2019-12-24 | 2022-08-05 | 信达生物制药(苏州)有限公司 | 融合蛋白在治疗年龄相关性黄斑变性中的应用 |
| JP2023517403A (ja) * | 2020-03-21 | 2023-04-26 | ラリクス・バイオサイエンス・リミテッド・ライアビリティ・カンパニー | Ace2および補体経路の二重特異性および三重特異性機能性分子ならびにその使用 |
| CN115803009A (zh) | 2020-05-08 | 2023-03-14 | 瑞泽恩制药公司 | 用于治疗眼病和癌症的vegf阱和微阱及方法 |
| US20230242633A1 (en) * | 2020-07-07 | 2023-08-03 | Kanaph Therapeutics Inc. | Fusion protein including complement pathway inhibitor and angiogenesis inhibitor and use thereof |
| AU2021362770A1 (en) * | 2020-10-16 | 2022-12-08 | Gyroscope Therapeutics Limited | Nucleic acid encoding an anti-VEGF entity and a negative complement regulator and uses thereof for the treatment of age-related macular degeneration |
| CN113041360A (zh) * | 2021-04-01 | 2021-06-29 | 深圳廷美奥生物技术有限公司 | 一种用于治疗年龄相关性黄斑变性的药物 |
| EP4386009A4 (en) * | 2021-08-09 | 2025-05-14 | Yuanpu Biotechnology (Wuhan) Co., Ltd. | BISPECIFIC FUSION POLYPEPTIDE AND USE THEREOF |
| TW202328211A (zh) * | 2021-11-19 | 2023-07-16 | 圓祥生技股份有限公司 | 針對補體途徑的雙功能融合蛋白、其醫藥組成物及其治療或預防補體相關疾病的用途 |
| KR20230105972A (ko) * | 2022-01-05 | 2023-07-12 | 주식회사 카나프테라퓨틱스 | 혈관신생 억제제가 결합된 항-C3b 항체 또는 항-C5 항체 및 이의 용도 |
| CN116675777B (zh) * | 2022-02-23 | 2025-07-08 | 中山光度生物医药有限公司 | 包含补体抑制结构域的多特异性配体结合分子及其用途 |
| GB202203627D0 (en) | 2022-03-16 | 2022-04-27 | Univ Manchester | Agents for treating complement-related disorders |
| US20250257106A1 (en) | 2022-04-11 | 2025-08-14 | Longbio Pharma (Suzhou) Co., Ltd. | Complement-inhibiting hybrid protein |
| US11723955B1 (en) | 2022-05-13 | 2023-08-15 | Allgenesis Biotherapeutics Inc. | VEGFR fusion protein pharmaceutical composition |
| CN118005802A (zh) | 2022-11-10 | 2024-05-10 | 天辰生物医药(苏州)有限公司 | 补体抑制杂合蛋白突变体及其抗体融合蛋白 |
| CN120476152A (zh) * | 2022-11-28 | 2025-08-12 | 深圳欧科健生物医药科技有限公司 | C5/vegf双特异性结合分子 |
| KR20250163297A (ko) | 2023-01-05 | 2025-11-20 | 컴플리먼트 테라퓨틱스 리미티드 | 보체 질환 치료제 및 치료방법 |
| WO2025021112A1 (zh) * | 2023-07-24 | 2025-01-30 | 佳吾益(北京)科技有限公司 | 开发mhc新抗原的工程化细胞 |
| WO2025109172A1 (en) * | 2023-11-24 | 2025-05-30 | Universität Ulm | Complement modulator |
| EP4559472A1 (en) * | 2023-11-24 | 2025-05-28 | Universität Ulm | Complement modulator |
| CN117467025B (zh) * | 2023-12-28 | 2024-04-16 | 上海鼎新基因科技有限公司 | 一种抗vegf和补体双功能融合蛋白及其应用 |
Family Cites Families (46)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| USRE30985E (en) | 1978-01-01 | 1982-06-29 | Serum-free cell culture media | |
| US4657760A (en) | 1979-03-20 | 1987-04-14 | Ortho Pharmaceutical Corporation | Methods and compositions using monoclonal antibody to human T cells |
| US4419446A (en) | 1980-12-31 | 1983-12-06 | The United States Of America As Represented By The Department Of Health And Human Services | Recombinant DNA process utilizing a papilloma virus DNA as a vector |
| NZ201705A (en) | 1981-08-31 | 1986-03-14 | Genentech Inc | Recombinant dna method for production of hepatitis b surface antigen in yeast |
| US4601978A (en) | 1982-11-24 | 1986-07-22 | The Regents Of The University Of California | Mammalian metallothionein promoter system |
| US4560655A (en) | 1982-12-16 | 1985-12-24 | Immunex Corporation | Serum-free cell culture medium and process for making same |
| US4657866A (en) | 1982-12-21 | 1987-04-14 | Sudhir Kumar | Serum-free, synthetic, completely chemically defined tissue culture media |
| DD266710A3 (de) | 1983-06-06 | 1989-04-12 | Ve Forschungszentrum Biotechnologie | Verfahren zur biotechnischen Herstellung van alkalischer Phosphatase |
| US4767704A (en) | 1983-10-07 | 1988-08-30 | Columbia University In The City Of New York | Protein-free culture medium |
| US4879231A (en) | 1984-10-30 | 1989-11-07 | Phillips Petroleum Company | Transformation of yeasts of the genus pichia |
| US5206344A (en) | 1985-06-26 | 1993-04-27 | Cetus Oncology Corporation | Interleukin-2 muteins and polymer conjugation thereof |
| GB8516415D0 (en) | 1985-06-28 | 1985-07-31 | Celltech Ltd | Culture of animal cells |
| US4927762A (en) | 1986-04-01 | 1990-05-22 | Cell Enterprises, Inc. | Cell culture medium with antioxidant |
| GB8610600D0 (en) | 1986-04-30 | 1986-06-04 | Novo Industri As | Transformation of trichoderma |
| IL89790A (en) * | 1988-04-01 | 2002-05-23 | Johns Hopking University | Nucleic acid sequences that encode and cells that produce cr1 protein and methods of production and purification |
| EP0435911B1 (en) | 1988-09-23 | 1996-03-13 | Cetus Oncology Corporation | Cell culture medium for enhanced cell growth, culture longevity and product expression |
| FR2646437B1 (fr) | 1989-04-28 | 1991-08-30 | Transgene Sa | Nouvelles sequences d'adn, leur application en tant que sequence codant pour un peptide signal pour la secretion de proteines matures par des levures recombinantes, cassettes d'expression, levures transformees et procede de preparation de proteines correspondant |
| EP0402226A1 (en) | 1989-06-06 | 1990-12-12 | Institut National De La Recherche Agronomique | Transformation vectors for yeast yarrowia |
| US5225212A (en) | 1989-10-20 | 1993-07-06 | Liposome Technology, Inc. | Microreservoir liposome composition and method |
| US5122469A (en) | 1990-10-03 | 1992-06-16 | Genentech, Inc. | Method for culturing Chinese hamster ovary cells to improve production of recombinant proteins |
| WO1993006217A1 (en) | 1991-09-19 | 1993-04-01 | Genentech, Inc. | EXPRESSION IN E. COLI OF ANTIBODY FRAGMENTS HAVING AT LEAST A CYSTEINE PRESENT AS A FREE THIOL, USE FOR THE PRODUCTION OF BIFUNCTIONAL F(ab')2 ANTIBODIES |
| ES2091684T3 (es) | 1992-11-13 | 1996-11-01 | Idec Pharma Corp | Aplicacion terapeutica de anticuerpos quimericos y radiomarcados contra el antigeno de diferenciacion restringida de los linfocitos b humanos para el tratamiento del linfoma de las celulas b. |
| CA2171953C (en) * | 1993-09-24 | 2003-02-04 | John P. Atkinson | Modified truncated complement system regulators |
| US5789199A (en) | 1994-11-03 | 1998-08-04 | Genentech, Inc. | Process for bacterial production of polypeptides |
| US5840523A (en) | 1995-03-01 | 1998-11-24 | Genetech, Inc. | Methods and compositions for secretion of heterologous polypeptides |
| GB9614871D0 (en) * | 1996-07-15 | 1996-09-04 | Smithkline Beecham Plc | Compounds |
| JP4723140B2 (ja) | 1999-06-08 | 2011-07-13 | リジェネロン・ファーマシューティカルズ・インコーポレイテッド | 改善された薬物動態特性を有する改変キメラポリペプチド |
| US7087411B2 (en) * | 1999-06-08 | 2006-08-08 | Regeneron Pharmaceuticals, Inc. | Fusion protein capable of binding VEGF |
| AU7902401A (en) * | 2000-08-01 | 2002-02-13 | Amgen Inc | C3b/c4b complement receptor-like molecules and uses thereof |
| MXPA03007186A (es) * | 2001-02-09 | 2005-07-01 | Human Genome Sciences Inc | Receptor de quimiocina de proteina g humana (ccr5) hdgnr10. |
| EP2292259A3 (en) | 2002-11-15 | 2011-03-23 | MUSC Foundation For Research Development | Complement receptor 2 targeted complement modulators |
| US20070155663A1 (en) | 2003-03-24 | 2007-07-05 | Rudolf Richter | Use of chemokine receptor agonists for stem cell transplantation |
| US20070148170A1 (en) | 2005-10-03 | 2007-06-28 | Desjarlais John R | Fc Variants With Optimized Fc Receptor Binding Properties |
| US20060134105A1 (en) | 2004-10-21 | 2006-06-22 | Xencor, Inc. | IgG immunoglobulin variants with optimized effector function |
| CA2621047A1 (en) | 2005-02-02 | 2006-08-24 | Regeneron Pharmaceuticals, Inc. | Method of treating eye injury with local administration of a vegf inhibitor |
| CN101384614A (zh) * | 2005-08-15 | 2009-03-11 | 加利福尼亚大学董事会 | Vegf活化的fas配体 |
| US8168584B2 (en) | 2005-10-08 | 2012-05-01 | Potentia Pharmaceuticals, Inc. | Methods of treating age-related macular degeneration by compstatin and analogs thereof |
| JP5345849B2 (ja) | 2005-10-08 | 2013-11-20 | ポテンシア ファーマシューティカルズ, インコーポレイテッド | 眼の障害のためのコンプスタチンおよびそのアナログ |
| WO2007047995A2 (en) * | 2005-10-21 | 2007-04-26 | Catalyst Biosciences, Inc. | Modified proteases that inhibit complement activation |
| AU2007261315B2 (en) | 2006-06-21 | 2012-10-25 | Musc Foundation For Research Development | Targeting complement factor H for treatment of diseases |
| WO2008048675A2 (en) * | 2006-10-20 | 2008-04-24 | Celldex Therapeutics, Inc. | Treatment for age-related macular degeneration and other diseases of the eye |
| US8268314B2 (en) * | 2008-10-08 | 2012-09-18 | Hoffmann-La Roche Inc. | Bispecific anti-VEGF/anti-ANG-2 antibodies |
| CN102317320A (zh) * | 2008-12-11 | 2012-01-11 | 韩国科学技术院 | 能够结合于VEGF-A和TNF-α的融合蛋白 |
| EP2417263B1 (en) * | 2009-04-09 | 2015-09-23 | ProteoVec Holding L.L.C. | Production of proteins using transposon-based vectors |
| CN102219859B (zh) * | 2011-05-20 | 2012-09-12 | 烟台荣昌生物工程有限公司 | 拮抗血管新生诱导因子的融合蛋白及其用途 |
| CN110078831A (zh) | 2011-12-01 | 2019-08-02 | 圆祥生命科技股份有限公司 | 补体和vegf途径的蛋白质抑制剂及其使用方法 |
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Also Published As
| Publication number | Publication date |
|---|---|
| US20150079084A1 (en) | 2015-03-19 |
| CN110078831A (zh) | 2019-08-02 |
| JP2015500811A (ja) | 2015-01-08 |
| AU2012318288B2 (en) | 2015-09-17 |
| WO2013082563A8 (en) | 2014-06-26 |
| EP2785744B1 (en) | 2017-10-04 |
| JP6138815B2 (ja) | 2017-05-31 |
| US9988611B2 (en) | 2018-06-05 |
| CA2857168C (en) | 2020-10-27 |
| US11518984B2 (en) | 2022-12-06 |
| CN104159926A (zh) | 2014-11-19 |
| DK2785744T3 (da) | 2017-11-27 |
| EP2785744A4 (en) | 2015-07-22 |
| EP2785744A1 (en) | 2014-10-08 |
| AU2012318288A1 (en) | 2013-06-20 |
| US20180312819A1 (en) | 2018-11-01 |
| WO2013082563A1 (en) | 2013-06-06 |
| CN104159926B (zh) | 2019-02-01 |
| JP2017189167A (ja) | 2017-10-19 |
| CA2857168A1 (en) | 2013-06-06 |
| BR112014013205A2 (pt) | 2020-10-27 |
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