KR20220013459A - 섬유화 질환을 치료하기 위한 엔도글린 펩티드 - Google Patents
섬유화 질환을 치료하기 위한 엔도글린 펩티드 Download PDFInfo
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| CZ291047B6 (cs) | 1992-10-28 | 2002-12-11 | Genentech, Inc. | Farmaceutický prostředek obsahující antagonisty faktoru růstu vaskulárních endoteliálních buněk |
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| JPH08511420A (ja) | 1993-06-16 | 1996-12-03 | セルテック・セラピューテイクス・リミテッド | 抗 体 |
| US5541087A (en) | 1994-09-14 | 1996-07-30 | Fuji Immunopharmaceuticals Corporation | Expression and export technology of proteins as immunofusins |
| IL117645A (en) | 1995-03-30 | 2005-08-31 | Genentech Inc | Vascular endothelial cell growth factor antagonists for use as medicaments in the treatment of age-related macular degeneration |
| US6423501B2 (en) | 1996-12-13 | 2002-07-23 | Beth Israel Deaconess Medical Center | Calcium-independent negative regulation by CD81 of receptor signaling |
| MX9701946A (es) | 1997-03-14 | 1998-04-30 | Arturo Jimenez Bayardo | Solucion oftalmica transportadora. |
| US6884879B1 (en) | 1997-04-07 | 2005-04-26 | Genentech, Inc. | Anti-VEGF antibodies |
| KR100856995B1 (ko) | 1997-04-07 | 2008-09-04 | 제넨테크, 인크. | 인간화 항체 및 인간화 항체의 제조 방법 |
| US20020032315A1 (en) | 1997-08-06 | 2002-03-14 | Manuel Baca | Anti-vegf antibodies |
| ATE293640T1 (de) | 1997-04-07 | 2005-05-15 | Genentech Inc | Anti-vegf antikörper |
| WO1998047531A2 (en) | 1997-04-21 | 1998-10-29 | Arch Development Corporation | Fc receptor non-binding anti-cd3 monoclonal antibodies deliver a partial tcr signal and induce clonal anergy |
| US6194551B1 (en) | 1998-04-02 | 2001-02-27 | Genentech, Inc. | Polypeptide variants |
| ES2292236T3 (es) | 1998-04-02 | 2008-03-01 | Genentech, Inc. | Variantes de anticuerpos y sus fragmentos. |
| US6703020B1 (en) | 1999-04-28 | 2004-03-09 | Board Of Regents, The University Of Texas System | Antibody conjugate methods for selectively inhibiting VEGF |
| MEP13708A (en) | 2000-06-23 | 2010-06-10 | Bayer Schering Pharma Ag | Combinations and compositions which interfere with vegf/vegf and angiopoietin/tie receptor function and their use (ii) |
| US20040142325A1 (en) | 2001-09-14 | 2004-07-22 | Liat Mintz | Methods and systems for annotating biomolecular sequences |
| PL1638941T3 (pl) | 2003-05-22 | 2010-11-30 | Abbvie Bahamas Ltd | Indazolowe, benzizoksazolowe i benzizotiazolowe inhibitory kinaz |
| RS20181002A1 (sr) | 2003-05-30 | 2018-12-31 | Genentech Inc | Tretman sa anti-vegf antitelima |
| WO2005044853A2 (en) | 2003-11-01 | 2005-05-19 | Genentech, Inc. | Anti-vegf antibodies |
| US20050106667A1 (en) | 2003-08-01 | 2005-05-19 | Genentech, Inc | Binding polypeptides with restricted diversity sequences |
| US20090286271A1 (en) | 2006-05-31 | 2009-11-19 | Karumanchi Ananth S | Methods of Diagnosing and Treating Complications of Pregnancy |
| WO2007143023A1 (en) | 2006-05-31 | 2007-12-13 | Beth Israel Deaconess Medical Center | Soluble endoglin compounds and uses thereof for the treatment and prevention of cancer |
| ES2612755T3 (es) | 2006-11-02 | 2017-05-18 | Acceleron Pharma, Inc. | Antagonistas de receptor y ligando de ALK1 y usos de los mismos |
| WO2008151078A1 (en) | 2007-06-01 | 2008-12-11 | Wyeth | Methods and compositions for modulating bmp-10 activity |
| EP2209003A1 (en) * | 2009-01-16 | 2010-07-21 | F. Hoffmann-Roche AG | Means and methods for differentiating between fibrosis and cirrhosis |
| US20100210713A1 (en) * | 2009-01-16 | 2010-08-19 | The General Hospital Corporation | Regeneration and survival of cardiac progenitors and cardiomyocytes with a stretch activated transcription factor |
| CN102548617B (zh) * | 2009-03-30 | 2017-11-07 | 阿塞勒隆制药公司 | Bmp‑alk3拮抗剂和促进骨生长的用途 |
| US20120183543A1 (en) * | 2009-05-08 | 2012-07-19 | Novartis Ag | Diagnostic biomarkers for fibrotic disorders |
| US8795663B2 (en) | 2010-01-12 | 2014-08-05 | Beth Israel Deaconess Medical Center, Inc. | Soluble endoglin and uses thereof |
| CA2833747C (en) * | 2011-04-20 | 2022-10-18 | Asya Grinberg | Endoglin polypeptides and uses thereof |
| EP2739645B1 (en) * | 2011-08-01 | 2018-12-19 | Tufts Medical Center, Inc. | Endoglin-specific antibody for use in a method of treating heart failure and related conditions |
| US10214590B2 (en) | 2013-09-20 | 2019-02-26 | Tufts Medical Center, Inc. | Inhibitors of endoglin activity for the treatment of fibrosis |
| EP3060235B1 (en) | 2013-10-25 | 2020-12-02 | Acceleron Pharma Inc. | Endoglin peptides to treat fibrotic diseases |
| CA2966905A1 (en) | 2014-11-12 | 2016-05-19 | Tracon Pharmaceuticals, Inc. | Anti-endoglin antibodies and uses thereof |
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2014
- 2014-10-24 EP EP14796626.1A patent/EP3060235B1/en active Active
- 2014-10-24 EP EP20201627.5A patent/EP3851118A1/en not_active Withdrawn
- 2014-10-24 US US14/522,891 patent/US20150202260A1/en not_active Abandoned
- 2014-10-24 KR KR1020227001830A patent/KR20220013459A/ko not_active Ceased
- 2014-10-24 CN CN201480070781.XA patent/CN105899225A/zh active Pending
- 2014-10-24 EA EA202090707A patent/EA202090707A1/ru unknown
- 2014-10-24 EA EA201690855A patent/EA035481B1/ru not_active IP Right Cessation
- 2014-10-24 CA CA2928708A patent/CA2928708A1/en not_active Abandoned
- 2014-10-24 JP JP2016526141A patent/JP6546587B2/ja not_active Expired - Fee Related
- 2014-10-24 AU AU2014339898A patent/AU2014339898B2/en not_active Ceased
- 2014-10-24 KR KR1020167013678A patent/KR102354787B1/ko not_active Expired - Fee Related
- 2014-10-24 WO PCT/US2014/062147 patent/WO2015061666A1/en not_active Ceased
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Also Published As
| Publication number | Publication date |
|---|---|
| US20200164029A1 (en) | 2020-05-28 |
| EA201690855A1 (ru) | 2016-10-31 |
| EP3851118A1 (en) | 2021-07-21 |
| KR102354787B1 (ko) | 2022-01-24 |
| WO2015061666A1 (en) | 2015-04-30 |
| CA2928708A1 (en) | 2015-04-30 |
| AU2020244463A1 (en) | 2020-10-29 |
| AU2014339898B2 (en) | 2020-07-23 |
| AU2014339898A1 (en) | 2016-05-26 |
| EP3060235A1 (en) | 2016-08-31 |
| US20150202260A1 (en) | 2015-07-23 |
| JP2022058352A (ja) | 2022-04-12 |
| JP2016535741A (ja) | 2016-11-17 |
| EA035481B1 (ru) | 2020-06-23 |
| US11590201B2 (en) | 2023-02-28 |
| CN105899225A (zh) | 2016-08-24 |
| JP6546587B2 (ja) | 2019-07-17 |
| EA202090707A1 (ru) | 2020-12-30 |
| EP3060235B1 (en) | 2020-12-02 |
| JP2019196364A (ja) | 2019-11-14 |
| JP6994481B2 (ja) | 2022-02-04 |
| KR20160066553A (ko) | 2016-06-10 |
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