ES2345113T3 - Peptidos de la familia amilina y metodos para su obtencion y utilizacion. - Google Patents
Peptidos de la familia amilina y metodos para su obtencion y utilizacion. Download PDFInfo
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- ES2345113T3 ES2345113T3 ES05723040T ES05723040T ES2345113T3 ES 2345113 T3 ES2345113 T3 ES 2345113T3 ES 05723040 T ES05723040 T ES 05723040T ES 05723040 T ES05723040 T ES 05723040T ES 2345113 T3 ES2345113 T3 ES 2345113T3
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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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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Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
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- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
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| US543275P | 2004-02-11 | ||
| US55044704P | 2004-03-04 | 2004-03-04 | |
| US550447P | 2004-03-04 |
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| RU2385878C2 (ru) * | 2004-02-11 | 2010-04-10 | Амилин Фармасьютикалз, Инк. | Пептид, обладающий свойствами амилина (варианты), и его применение (варианты) |
| US8076288B2 (en) | 2004-02-11 | 2011-12-13 | Amylin Pharmaceuticals, Inc. | Hybrid polypeptides having glucose lowering activity |
| EP2286840A3 (en) | 2004-11-01 | 2013-09-04 | Amylin Pharmaceuticals, LLC | Treatment of obesity and related diseases |
| US8394765B2 (en) | 2004-11-01 | 2013-03-12 | Amylin Pharmaceuticals Llc | Methods of treating obesity with two different anti-obesity agents |
| EP2258382A3 (en) | 2005-03-31 | 2014-05-14 | Amylin Pharmaceuticals, LLC | Amylin and amylin agonists for treating psychiatric diseases and disorders |
| EP2120985B1 (en) | 2007-02-05 | 2012-06-27 | Amylin Pharmaceuticals, Inc. | FN-38 peptides for use in the treatment of psychotic and anxiety disorders |
| WO2009156473A1 (en) * | 2008-06-25 | 2009-12-30 | Novo Nordisk A/S | Derivatised hybrid peptides of amylin and salmon calcitonin |
| WO2010014225A2 (en) | 2008-07-30 | 2010-02-04 | Biomarin Pharmaceutical Inc. | Assays for detection of phenylalanine ammonia-lyase and antibodies to phenylalanine ammonia-lyase |
| CN102292346B (zh) * | 2009-01-22 | 2015-12-02 | 关键生物科学有限公司 | 肥胖的治疗 |
| RU2537181C2 (ru) * | 2009-03-12 | 2014-12-27 | Нордик Байосайенс А/С | Лечение диабета и метаболического синдрома |
| US8748375B2 (en) | 2009-03-17 | 2014-06-10 | Amylin Pharmaceuticals, Llc | Methods for affecting body composition using amylin agonists |
| WO2010118384A2 (en) | 2009-04-10 | 2010-10-14 | Amylin Pharmaceuticals, Inc. | Amylin agonist compounds for estrogen-deficient mammals |
| AU2010321587A1 (en) | 2009-11-23 | 2012-06-07 | Amylin Pharmaceuticals, Inc. | Polypeptide Conjugate |
| GB201001333D0 (en) | 2010-01-27 | 2010-03-17 | Imp Innovations Ltd | Novel compounds and their effects on feeding behaviour |
| ES2582459T3 (es) * | 2010-02-04 | 2016-09-13 | Biomarin Pharmaceutical Inc. | Composiciones de variantes de fenilalanina amoníaco-liasa de procariotas y métodos de uso de sus composiciones |
| ES2630031T3 (es) | 2010-09-28 | 2017-08-17 | Aegerion Pharmaceuticals, Inc. | Un polipéptido de leptina pinnípedo-humano quimérico con solubilidad aumentada |
| WO2012050923A2 (en) | 2010-09-28 | 2012-04-19 | Amylin Pharmaceuticals, Inc. | Engineered polypeptides having enhanced duration of action |
| CN103458916B (zh) | 2011-04-07 | 2016-08-10 | 小利兰·斯坦福大学托管委员会 | 长效肽类似物 |
| CA2837104A1 (en) * | 2011-05-25 | 2012-11-29 | Amylin Pharmaceuticals, Llc | Amylin peptides and derivatives and uses thereof |
| WO2012160212A1 (en) | 2011-05-25 | 2012-11-29 | Camurus Ab | Peptide controlled-release formulations |
| JP2014521594A (ja) | 2011-05-25 | 2014-08-28 | アミリン・ファーマシューティカルズ，リミテッド・ライアビリティ・カンパニー | 長持続期間デュアルホルモンコンジュゲート |
| ES2732475T3 (es) | 2011-07-08 | 2019-11-22 | Aegerion Pharmaceuticals Inc | Polipéptidos modificados por ingeniería genética que tienen una duración potenciada de la acción y una inmunogenicidad reducida |
| JP6006309B2 (ja) | 2011-07-08 | 2016-10-12 | アミリン・ファーマシューティカルズ, リミテッド・ライアビリティ・カンパニーAmylin Pharmaceuticals, Llc | 作用持続期間が増大し、免疫原性が減少した操作されたポリペプチド |
| US20140249076A1 (en) * | 2011-10-18 | 2014-09-04 | Astrazeneca Pharmaceuticals Lp | Amylin-calcitonin chimeric peptides conjugated to duration enhancing moieties |
| US9533022B2 (en) | 2011-11-02 | 2017-01-03 | KeyBioscience A/S | Peptide analogs for treating diseases and disorders |
| BR112014010701A2 (pt) | 2011-11-02 | 2020-06-23 | Keybioscience Ag | Uso de um peptídeo |
| CA2861392C (en) * | 2012-01-26 | 2021-08-17 | Christopher J. Soares | Peptide antagonists of the calcitonin cgrp family of peptide hormones and their use |
| CA2868688A1 (en) | 2012-04-03 | 2013-10-10 | Trustees Of Boston University | Compositions, methods and assays comprising amylin or amlyin analogs for abeta-peptide mediated disorders |
| US8575091B1 (en) | 2012-04-19 | 2013-11-05 | Novo Nordisk A/S | Amylin analogues and pharmaceutical compositions thereof |
| UA116217C2 (uk) | 2012-10-09 | 2018-02-26 | Санофі | Пептидна сполука як подвійний агоніст рецепторів glp1-1 та глюкагону |
| HK1211232A1 (en) | 2012-12-21 | 2016-05-20 | Sanofi | Exendin-4 derivatives as dual glp1/gip or trigonal glp1/gip/glucagon agonists |
| BR102013017626A2 (pt) * | 2013-06-14 | 2015-02-10 | Univ Rio De Janeiro | Bioconjugados não aglomerantes de amilinomiméticos com polietilenoglicol, uso de bioconjugados não aglomerantes de amilinomiméticos com polietilenoglicol, composições farmacêuticas de baixa toxicidade, adjuvante para a prevenção ou tratamento das doenças, medicamento, método de tratamento ou prevenção de doenças. |
| WO2015017455A1 (en) * | 2013-07-30 | 2015-02-05 | Soares Christopher J | Cgrp agonist peptides |
| AR097701A1 (es) * | 2013-09-19 | 2016-04-13 | Zealand Pharma As | Análogos de amilina |
| EP3080152A1 (en) | 2013-12-13 | 2016-10-19 | Sanofi | Non-acylated exendin-4 peptide analogues |
| WO2015086728A1 (en) | 2013-12-13 | 2015-06-18 | Sanofi | Exendin-4 peptide analogues as dual glp-1/gip receptor agonists |
| TW201609799A (zh) | 2013-12-13 | 2016-03-16 | 賽諾菲公司 | 雙重ｇｌｐ－１／ｇｉｐ受體促效劑 |
| WO2015086733A1 (en) | 2013-12-13 | 2015-06-18 | Sanofi | Dual glp-1/glucagon receptor agonists |
| TW201625669A (zh) | 2014-04-07 | 2016-07-16 | 賽諾菲公司 | 衍生自艾塞那肽－４（Ｅｘｅｎｄｉｎ－４）之肽類雙重ＧＬＰ－１／升糖素受體促效劑 |
| TW201625670A (zh) | 2014-04-07 | 2016-07-16 | 賽諾菲公司 | 衍生自ｅｘｅｎｄｉｎ－４之雙重ｇｌｐ－１／升糖素受體促效劑 |
| TW201625668A (zh) | 2014-04-07 | 2016-07-16 | 賽諾菲公司 | 作為胜肽性雙重ｇｌｐ－１／昇糖素受體激動劑之艾塞那肽－４衍生物 |
| US9932381B2 (en) | 2014-06-18 | 2018-04-03 | Sanofi | Exendin-4 derivatives as selective glucagon receptor agonists |
| AR103954A1 (es) | 2015-03-18 | 2017-06-14 | Zealand Pharma As | Análogos de amilina |
| AR105319A1 (es) | 2015-06-05 | 2017-09-27 | Sanofi Sa | Profármacos que comprenden un conjugado agonista dual de glp-1 / glucagón conector ácido hialurónico |
| AR105284A1 (es) | 2015-07-10 | 2017-09-20 | Sanofi Sa | Derivados de exendina-4 como agonistas peptídicos duales específicos de los receptores de glp-1 / glucagón |
| BR102015031283A2 (pt) * | 2015-12-14 | 2018-09-18 | Univ Rio De Janeiro | Bioconjugado de amilina humana ou de análogos de amilinanão agregantes, composição, métodos para a preparação deuma composição, para o tratamento de uma doença oucondição e para estabilizar um composto amilino-mimético, e,medicamento |
| US11034745B2 (en) | 2016-01-04 | 2021-06-15 | Adepthera Llc | Superagonist polypeptide analogs of adrenomedullin and intermedin peptide hormones |
| US11701409B2 (en) | 2016-02-09 | 2023-07-18 | Adepthera Llc | Dosing and use of long-acting CLR/ramp agonists |
| EP4316595A3 (en) | 2016-09-02 | 2024-04-17 | Christopher J. Soares | Use of cgrp receptor antagonists in treating glaucoma |
| TWI784968B (zh) | 2016-09-09 | 2022-12-01 | 丹麥商西蘭製藥公司 | 澱粉素類似物 |
| US20190153059A1 (en) | 2017-06-30 | 2019-05-23 | Adepthera Llc | Peptide analogs |
| HRP20240485T1 (hr) | 2017-08-24 | 2024-07-05 | Novo Nordisk A/S | Pripravci glp-1 i njihova upotreba |
| WO2021056106A1 (en) | 2019-09-23 | 2021-04-01 | Dds Research Inc. | Lipid vesicle compositions with penetration enhancing agents |
| PE20230819A1 (es) | 2020-02-18 | 2023-05-19 | Novo Nordisk As | Composiciones y usos de glp-1 |
| MX2023011157A (es) * | 2021-03-24 | 2024-01-25 | Glo Pharma Inc | Peptidos y metodos para reducir la pigmentacion de la piel. |
| WO2024189611A1 (en) * | 2023-03-13 | 2024-09-19 | Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd. | Stabilized analogues of calcitonin |
Family Cites Families (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6936694B1 (en) | 1982-05-06 | 2005-08-30 | Intermune, Inc. | Manufacture and expression of large structural genes |
| GB8720115D0 (en) * | 1987-08-26 | 1987-09-30 | Cooper G J S | Treatment of diabetes mellitus |
| GB8709871D0 (en) | 1987-04-27 | 1987-06-03 | Turner R C | Peptides |
| JP2796388B2 (ja) | 1988-05-13 | 1998-09-10 | アムジエン・インコーポレーテツド | Ｇ−ｃｓｆの精製方法 |
| US5264372A (en) | 1991-03-15 | 1993-11-23 | Amylin Pharmaceuticals, Inc. | Receptor-based screening methods for amylin agonists and antagonists |
| HU222249B1 (hu) | 1991-03-08 | 2003-05-28 | Amylin Pharmaceuticals Inc. | Eljárás amilin agonista peptidszármazékok és ezeket tartalmazó gyógyszerkészítmények előállítására |
| US5580953A (en) * | 1991-08-14 | 1996-12-03 | Amylin Pharmaceuticals, Inc. | Amylin antagonist peptides and uses therefor |
| US5912015A (en) * | 1992-03-12 | 1999-06-15 | Alkermes Controlled Therapeutics, Inc. | Modulated release from biocompatible polymers |
| JPH06256210A (ja) * | 1993-03-10 | 1994-09-13 | Hoechst Japan Ltd | 骨関連転写制御因子様タンパク質およびその製造法 |
| ZA943251B (en) | 1993-05-12 | 1995-01-16 | Univ Cincinnati | Amylin antagonists ans agonists. |
| AU7685894A (en) * | 1993-09-07 | 1995-03-27 | Amylin Pharmaceuticals, Inc. | Methods for regulating gastrointestinal motility |
| US5766627A (en) * | 1993-11-16 | 1998-06-16 | Depotech | Multivescular liposomes with controlled release of encapsulated biologically active substances |
| US6143718A (en) * | 1995-06-07 | 2000-11-07 | Amylin Pharmaceuticals, Inc. | Treatment of Type II diabetes mellutis with amylin agonists |
| US5739106A (en) * | 1995-06-07 | 1998-04-14 | Rink; Timothy J. | Appetite regulating compositions |
| US5686511A (en) | 1996-06-28 | 1997-11-11 | The Valspar Corporation | Esterifying epoxy resin with carboxyl polymer and quenching |
| US5677279A (en) | 1996-12-16 | 1997-10-14 | Amylin Pharmaceuticals, Inc. | Methods and compositions for treating pain with amylin or agonists thereof |
| EP0996459B1 (en) | 1997-01-07 | 2005-09-21 | Amylin Pharmaceuticals, Inc. | Use of exendins and agonists thereof for the reduction of food intake |
| US6410511B2 (en) | 1997-01-08 | 2002-06-25 | Amylin Pharmaceuticals, Inc. | Formulations for amylin agonist peptides |
| US7312196B2 (en) * | 1997-01-08 | 2007-12-25 | Amylin Pharmaceuticals, Inc. | Formulations for amylin agonist peptides |
| US7101853B2 (en) | 1997-05-06 | 2006-09-05 | Amylin Pharmaceuticals, Inc. | Method for treating or preventing gastritis using amylin or amylin agonists |
| US20040022807A1 (en) * | 1998-06-05 | 2004-02-05 | Duft Bradford J | Methods for treating obesity |
| CA2299425A1 (en) | 1997-08-08 | 1999-02-18 | Amylin Pharmaceuticals, Inc. | Novel exendin agonist compounds |
| US7157555B1 (en) | 1997-08-08 | 2007-01-02 | Amylin Pharmaceuticals, Inc. | Exendin agonist compounds |
| US7220721B1 (en) | 1997-11-14 | 2007-05-22 | Amylin Pharmaceuticals, Inc. | Exendin agonist peptides |
| WO1999025727A2 (en) | 1997-11-14 | 1999-05-27 | Amylin Pharmaceuticals, Inc. | Novel exendin agonist compounds |
| ATE383867T1 (de) | 1997-11-14 | 2008-02-15 | Amylin Pharmaceuticals Inc | Neuartige exendin agonisten |
| US6936584B1 (en) * | 1998-02-13 | 2005-08-30 | Amylin Pharmaceuticals, Inc. | Mixed amylin activity compounds |
| EP1053001B1 (en) * | 1998-02-13 | 2010-12-15 | Amylin Pharmaceuticals, Inc. | Novel mixed amylin activity compounds |
| US6087334A (en) * | 1998-08-21 | 2000-07-11 | Amylin Pharmaceuticals, Inc. | Anti-diabetic peptides |
| US6194006B1 (en) * | 1998-12-30 | 2001-02-27 | Alkermes Controlled Therapeutics Inc. Ii | Preparation of microparticles having a selected release profile |
| RU2166258C2 (ru) * | 1999-07-01 | 2001-05-10 | Общество с ограниченной ответственностью Научно-производственный центр "Витиус" | Композиция фиточая |
| US6458387B1 (en) | 1999-10-18 | 2002-10-01 | Epic Therapeutics, Inc. | Sustained release microspheres |
| US6264987B1 (en) * | 2000-05-19 | 2001-07-24 | Alkermes Controlled Therapeutics Inc. Ii | Method for preparing microparticles having a selected polymer molecular weight |
| US6296842B1 (en) * | 2000-08-10 | 2001-10-02 | Alkermes Controlled Therapeutics, Inc. | Process for the preparation of polymer-based sustained release compositions |
| US20030026182A1 (en) * | 2001-08-06 | 2003-02-06 | Fischer Michael C. | Method and system for write clock synchronization in a data storage system |
| EP1631308B1 (en) * | 2003-05-30 | 2013-07-31 | Amylin Pharmaceuticals, LLC | Novel methods and compositions for enhanced transmucosal delivery of peptides and proteins |
| EP1718665B1 (en) | 2004-02-11 | 2013-04-10 | Amylin Pharmaceuticals, LLC | Hybrid polypeptides with selectable properties |
| WO2005077094A2 (en) * | 2004-02-11 | 2005-08-25 | Amylin Pharmaceuticals, Inc. | Pancreatic polypeptide family motifs and polypeptides comprising the same |
| RU2385878C2 (ru) * | 2004-02-11 | 2010-04-10 | Амилин Фармасьютикалз, Инк. | Пептид, обладающий свойствами амилина (варианты), и его применение (варианты) |
| US7399744B2 (en) * | 2004-03-04 | 2008-07-15 | Amylin Pharmaceuticals, Inc. | Methods for affecting body composition |
| MX2007006830A (es) | 2004-12-13 | 2008-02-07 | Amylin Pharmaceuticals Inc | Porciones de la familia del polipeptido pancreatico, polipeptidos y metodos que comprenden las mismas. |
| EP2258382A3 (en) * | 2005-03-31 | 2014-05-14 | Amylin Pharmaceuticals, LLC | Amylin and amylin agonists for treating psychiatric diseases and disorders |
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- 2005-02-11 BR BRPI0507623-4A patent/BRPI0507623A/pt not_active IP Right Cessation
- 2005-02-11 WO PCT/US2005/004631 patent/WO2006083254A1/en not_active Ceased
- 2005-02-11 AT AT05723040T patent/ATE471340T1/de not_active IP Right Cessation
- 2005-02-11 AU AU2005320351A patent/AU2005320351B2/en not_active Ceased
- 2005-02-11 JP JP2007501804A patent/JP2008500281A/ja active Pending
- 2005-02-11 CA CA002556226A patent/CA2556226A1/en not_active Abandoned
- 2005-02-11 EP EP05723040A patent/EP1716172B1/en not_active Expired - Lifetime
- 2005-02-11 ES ES05723040T patent/ES2345113T3/es not_active Expired - Lifetime
- 2005-02-11 EP EP10006105A patent/EP2233497A3/en not_active Withdrawn
- 2005-02-11 NZ NZ571824A patent/NZ571824A/en not_active IP Right Cessation
- 2005-02-11 DE DE602005021858T patent/DE602005021858D1/de not_active Expired - Lifetime
-
2006
- 2006-08-02 IL IL177230A patent/IL177230A0/en unknown
- 2006-09-08 KR KR1020067018379A patent/KR101196122B1/ko not_active Expired - Fee Related
-
2009
- 2009-12-17 IL IL202795A patent/IL202795A0/en unknown
-
2010
- 2010-08-20 AU AU2010212468A patent/AU2010212468A1/en not_active Ceased
-
2012
- 2012-02-01 US US13/364,250 patent/US8598120B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| IL202795A0 (en) | 2011-07-31 |
| US8598120B2 (en) | 2013-12-03 |
| EP1716172B1 (en) | 2010-06-16 |
| IL177230A0 (en) | 2006-12-10 |
| EP2233497A2 (en) | 2010-09-29 |
| AU2010212468A1 (en) | 2010-09-09 |
| ATE471340T1 (de) | 2010-07-15 |
| NZ571824A (en) | 2010-04-30 |
| NZ549332A (en) | 2008-11-28 |
| WO2006083254A1 (en) | 2006-08-10 |
| KR101196122B1 (ko) | 2012-12-18 |
| US20120196796A1 (en) | 2012-08-02 |
| EP1716172A1 (en) | 2006-11-02 |
| CA2556226A1 (en) | 2006-08-10 |
| AU2005320351A8 (en) | 2008-12-18 |
| RU2385878C2 (ru) | 2010-04-10 |
| AU2005320351B2 (en) | 2010-06-03 |
| JP2008500281A (ja) | 2008-01-10 |
| AU2005320351A1 (en) | 2006-08-31 |
| BRPI0507623A (pt) | 2007-07-03 |
| US8114958B2 (en) | 2012-02-14 |
| RU2006132293A (ru) | 2008-03-20 |
| KR20070008589A (ko) | 2007-01-17 |
| DE602005021858D1 (de) | 2010-07-29 |
| US20080274952A1 (en) | 2008-11-06 |
| EP2233497A3 (en) | 2011-01-12 |
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