JP2005535569A5 - - Google Patents

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Publication number
JP2005535569A5
JP2005535569A5 JP2003581803A JP2003581803A JP2005535569A5 JP 2005535569 A5 JP2005535569 A5 JP 2005535569A5 JP 2003581803 A JP2003581803 A JP 2003581803A JP 2003581803 A JP2003581803 A JP 2003581803A JP 2005535569 A5 JP2005535569 A5 JP 2005535569A5
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JP
Japan
Prior art keywords
pharmaceutical composition
glp
composition according
val
amide
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
JP2003581803A
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English (en)
Japanese (ja)
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JP2005535569A (ja
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Publication date
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Priority claimed from PCT/DK2003/000216 external-priority patent/WO2003084563A1/en
Publication of JP2005535569A publication Critical patent/JP2005535569A/ja
Publication of JP2005535569A5 publication Critical patent/JP2005535569A5/ja
Withdrawn legal-status Critical Current

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JP2003581803A 2002-04-04 2003-04-02 Glp−1アゴニスト及び心臓血管合併症 Withdrawn JP2005535569A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DKPA200200499 2002-04-04
US37525502P 2002-04-23 2002-04-23
PCT/DK2003/000216 WO2003084563A1 (en) 2002-04-04 2003-04-02 Glp-1 agonist and cardiovascular complications

Publications (2)

Publication Number Publication Date
JP2005535569A JP2005535569A (ja) 2005-11-24
JP2005535569A5 true JP2005535569A5 (https=) 2006-05-25

Family

ID=28793124

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2003581803A Withdrawn JP2005535569A (ja) 2002-04-04 2003-04-02 Glp−1アゴニスト及び心臓血管合併症

Country Status (5)

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US (7) US20030220255A1 (https=)
EP (1) EP1494704A1 (https=)
JP (1) JP2005535569A (https=)
AU (1) AU2003226913A1 (https=)
WO (1) WO2003084563A1 (https=)

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UA97707C2 (ru) * 2007-11-14 2012-03-12 Амилин Фармасьютикалз, Инк. Способы лечения ожирения и заболеваний, расстройств, связанных с ожирением
PT2373681T (pt) 2008-12-10 2017-04-11 Glaxosmithkline Llc Composições farmacêuticas de albiglutida
US8691763B2 (en) 2010-05-04 2014-04-08 Glaxosmithkline Llc Methods for treating or preventing cardiovascular disorders and providing cardiovascular protection
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UA116217C2 (uk) 2012-10-09 2018-02-26 Санофі Пептидна сполука як подвійний агоніст рецепторів glp1-1 та глюкагону
AU2013366692B2 (en) 2012-12-21 2017-11-23 Sanofi Dual GLP1/GIP or trigonal GLP1/GIP/Glucagon agonists
US20160151461A1 (en) * 2013-03-14 2016-06-02 The Trustees Of The University Of Pennsylvania Cardio-Metabolic and Vascular Effects of GLP-1 Metabolites
EP3080154B1 (en) 2013-12-13 2018-02-07 Sanofi Dual glp-1/gip receptor agonists
WO2015086733A1 (en) 2013-12-13 2015-06-18 Sanofi Dual glp-1/glucagon receptor agonists
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
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
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
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
US9932381B2 (en) 2014-06-18 2018-04-03 Sanofi Exendin-4 derivatives as selective glucagon receptor agonists
AR105319A1 (es) 2015-06-05 2017-09-27 Sanofi Sa Profármacos que comprenden un conjugado agonista dual de glp-1 / glucagón conector ácido hialurónico
TW201706291A (zh) 2015-07-10 2017-02-16 賽諾菲公司 作為選擇性肽雙重glp-1/升糖素受體促效劑之新毒蜥外泌肽(exendin-4)衍生物
EP3337518A4 (en) * 2015-08-17 2019-06-12 Temple University Of The Commonwealth System Of Higher Education BAG3 COMPOSITIONS AND METHOD
US9968659B2 (en) * 2016-03-04 2018-05-15 Novo Nordisk A/S Liraglutide in cardiovascular conditions
CA3022535A1 (en) 2016-04-28 2017-11-02 Novo Nordisk A/S Semaglutide in cardiovascular conditions
KR102665710B1 (ko) 2017-08-24 2024-05-14 노보 노르디스크 에이/에스 Glp-1 조성물 및 그 용도
JP7761567B2 (ja) 2020-02-18 2025-10-28 ノヴォ ノルディスク アー/エス 医薬製剤

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WO2004050115A2 (en) * 2002-12-03 2004-06-17 Novo Nordisk A/S Combination treatment using exendin-4 and thiazolidinediones

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