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公开(公告)号:EP4440615A1
公开(公告)日:2024-10-09
申请号:EP21966037.0
申请日:2021-12-02
发明人: HAN, Zhaozhong , PAN, Hongya , PENG, Mengfan
IPC分类号: A61K39/395 , A61P25/00 , C12N15/62
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公开(公告)号:EP4424320A2
公开(公告)日:2024-09-04
申请号:EP24154518.5
申请日:2017-12-11
申请人: Zealand Pharma A/S
IPC分类号: A61K38/26
CPC分类号: C07K14/605 , A61K38/00 , A61P3/04 , A61P3/10 , A61K47/542
摘要: The invention relates to compounds having agonist activity at the GLP-1 (glucagon-like-peptide 1) and GLP-2 (glucagon-like peptide 2) receptors. The compounds find use, inter alia, in the prophylaxis or treatment of intestinal damage and dysfunction, regulation of body weight, and prophylaxis or treatment of metabolic dysfunction.
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公开(公告)号:EP4364751A3
公开(公告)日:2024-06-26
申请号:EP24161843.8
申请日:2019-04-05
发明人: THENNATI, Rajamannar , CHATURVEDI, Nishith , BURADE, Vinod Sampatrao , SHAHI, Pradeep Dinesh , NATARAJAN, Muthukumaran , NAGARAJA, Ravishankara Madavati , ZALAWADIA, Rishit Mansukhlal , PANDYA, Kunal , PATEL, Brijeshkumar , JOSHI, Dhiren Rameshchandra , SONI, Krunal Harishbhai , TIWARI, Abhishek , PATEL, Vipulkumar Shankarbhai
IPC分类号: C07K14/605 , A61K38/26
CPC分类号: C07K14/605 , A61K38/00
摘要: The present disclosure pertains to novel Glucagon like Peptide-1 (GLP-1) (7-37) analogs having an amino acid sequence with Leu or Ile at the C-terminal. The new analogs are potent GLP-1 agonists with reduced adverse effect and improved duration of action. The present disclosure further relates to acylated derivatives of the new analogs which have further improved potency and duration of action and are suitable for oral administration. The analogs of present disclosure may be useful in treatment of diabetes and obesity.
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公开(公告)号:EP4380962A1
公开(公告)日:2024-06-12
申请号:EP22852521.8
申请日:2022-08-04
发明人: SAJJA, Eswaraiah , GHOJALA, Venkat Reddy , MALLEPALLY, Venkat Reddy , SRINIVASAN, Thirumalai Rajan
IPC分类号: C07K14/605
CPC分类号: C07K14/605
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公开(公告)号:EP4362970A1
公开(公告)日:2024-05-08
申请号:EP22834208.5
申请日:2022-06-30
发明人: HSU, Henry , OTVOS, Laszlo
CPC分类号: A61P3/10 , C07K14/605 , C07K2319/0020130101 , C07K14/5759 , A61K47/64
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公开(公告)号:EP4357358A1
公开(公告)日:2024-04-24
申请号:EP22824309.3
申请日:2022-06-17
发明人: LIU, Weibing , HUANG, Xuchao , ZHANG, Xiaoqian , WU, Fangzhou , WANG, Lei , QU, Liang
IPC分类号: C07K14/605 , A61K38/26 , A61P3/10
CPC分类号: C07K14/605 , A61P3/10 , A61K38/26
摘要: A glucagon analog and the medical use thereof. Specifically, the glucagon analog has a significantly improved in vitro activity, excellent physical/chemical stability, and high solubility, and can be used to treat metabolic diseases such as hypoglycemia, obesity, and diabetes.
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公开(公告)号:EP4352088A1
公开(公告)日:2024-04-17
申请号:EP22819576.4
申请日:2022-06-08
发明人: AMSO, Zaid , SCHULTZ, Peter G. , SHEN, Weijun
IPC分类号: C07K14/605 , A61K38/26 , A61P3/10 , A61P3/04 , A61P1/00
CPC分类号: C07K14/605 , A61P3/10 , A61K38/26 , A61P1/00 , A61P3/04
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公开(公告)号:EP4351630A1
公开(公告)日:2024-04-17
申请号:EP22733387.9
申请日:2022-06-10
IPC分类号: A61K38/22 , A61K38/26 , C07K14/435 , C07K14/605 , C07K14/575 , A61P3/00 , A61P3/04 , A61P3/06 , A61P3/10 , A61P5/50 , A61P9/12
CPC分类号: A61K38/2278 , A61K38/26 , A61P3/10 , A61P3/04 , A61P3/00 , A61P3/06 , A61P5/50 , A61P9/12 , A61K38/22 , C07K14/645 , C07K14/605
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9.
公开(公告)号:EP3417871A1
公开(公告)日:2018-12-26
申请号:EP18165437.7
申请日:2010-11-11
发明人: Hagendorf, Annika , Hauck, Gerrit , Müller, Werner , Schoettle, Isabell , Siefke-Henzler, Verena , Tertsch, Katrin
CPC分类号: A61K47/10 , A61K9/0019 , A61K38/26 , A61K38/28 , A61K47/183 , C07K14/605 , C07K14/62 , A61K2300/00
摘要: Flüssige Zusammensetzung umfassend einen GLP-1-Agonisten oder/und ein pharmakologisch tolerierbares Salz davon, ein Insulin oder/und ein pharmakologisch tolerierbares Salz davon und gegebenenfalls mindestens einen pharmazeutisch akzeptablen Hilfsstoff, dadurch gekennzeichnet, dass sie Methionin enthält, gegebenenfalls als add-on Therapie mit Metformin.
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公开(公告)号:EP3405476A1
公开(公告)日:2018-11-28
申请号:EP17741733.4
申请日:2017-01-20
CPC分类号: C07K1/10 , C07K1/02 , C07K1/026 , C07K14/605
摘要: The invention discloses a method for the preparation of a peptide by liquid phase coupling of two fragments, an N-terminal fragment and a C-terminal fragment of the desired peptide, wherein the C-terminal fragment is protected on its C-terminal COOH by a psWang linker; the method is demonstrated with liraglutide wherein the C-terminal fragment carries the Palmitoyl-Glu-OtBu residue on the Lys.
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