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公开(公告)号:EP3484311B1
公开(公告)日:2023-12-06
申请号:EP17745586.2
申请日:2017-07-17
IPC分类号: A23L33/21 , A61K31/702 , A61K31/7016 , A23L2/52 , A61K31/07 , A61K31/197 , A61K31/198 , A61K31/28 , A61K31/355 , A61K31/375 , A61K31/401 , A61K31/405 , A61K31/4172 , A61K31/4188 , A61K31/4415 , A61K31/455 , A61K31/51 , A61K31/525
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2.
公开(公告)号:EP4281439A1
公开(公告)日:2023-11-29
申请号:EP22704251.2
申请日:2022-01-20
发明人: BOLLONG, Michael , SCHULTZ, Peter , SHAO, Sida , CHATTERJEE, Arnab , CHEN, Jian , ZHANG, Nan
IPC分类号: C07D207/16 , C07D487/04 , A61P11/00 , A61K31/401
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3.
公开(公告)号:EP4267247A1
公开(公告)日:2023-11-01
申请号:EP21912051.6
申请日:2021-12-21
IPC分类号: A61P31/00 , A61P31/10 , A61K31/401 , A23K30/18 , C12N1/20
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公开(公告)号:EP4180045A1
公开(公告)日:2023-05-17
申请号:EP20952613.6
申请日:2020-09-02
发明人: OLLERVIDES RUBIO, Paola Yazmín , ESPINOZA LEÓN, Sixto Serafín , CUAHUTENCOS ESCOBAR, Ernesto , GONZÁLEZ CANUDAS, Jorge Alejandro
IPC分类号: A61K31/64 , A61K31/155 , A61K31/401 , A61P3/10
摘要: This invention relates to an innovative stable immediate release drug for the treatment, control, and better management of type 2 diabetes mellitus containing a sulfonylurea such as glimepiride, a dipeptidyl peptidase-4 (DPP4) inhibitor such as vildagliptin, and a biguanidine such as metformin. At the same time, this invention allows solving a set of important technological challenges in the manufacture of said drug product due to the physicochemical properties and the difference in dosage of the synergistic combination of the drugs.
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5.
公开(公告)号:EP4165021A1
公开(公告)日:2023-04-19
申请号:EP21731503.5
申请日:2021-06-10
申请人: EPICS THERAPEUTICS
发明人: DUTHEUIL, Guillaume
IPC分类号: C07D207/16 , A61K31/401 , A61P29/00
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6.
公开(公告)号:EP4129407A1
公开(公告)日:2023-02-08
申请号:EP22193148.8
申请日:2015-02-25
发明人: GADHACHANDA, Venkat Rao , WANG, Qiuping , PAIS, Godwin , HASHIMOTO, Akihiro , CHEN, Dawei , WANG, Xiangzhu , ARARWAL, Atul , DESHPANDE, Milind , WILES, Jason Allan , PHADKE, Avinash S.
IPC分类号: A61P37/00 , A61K31/416 , A61K31/401 , C07D401/14 , C07D403/14
摘要: Compounds, methods of use, and processes for making inhibitors of complement factor D comprising Formulae X or VI, or a pharmaceutically acceptable salt or composition thereof are provided. The inhibitors described herein target factor D and inhibit or regulate the complement cascade at an early and essential point in the alternative complement pathway, and reduce factor D's ability to modulate the classical and lectin complement pathways. The inhibitors of factor D described herein are capable of reducing the excessive activation of complement, which has been linked to certain autoimmune, inflammatory, and neurodegenerative diseases, as well as ischemia-reperfusion injury and cancer.
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公开(公告)号:EP4091620A1
公开(公告)日:2022-11-23
申请号:EP22179865.5
申请日:2019-01-30
IPC分类号: A61K35/612 , A61K38/01 , A23L33/10 , A61K35/60 , A23K10/22 , A23J3/34 , A23K20/147 , A23L33/18 , A61K31/04 , A61K31/131 , A61K31/198 , A61K31/401 , A61K31/4172 , A61K33/00 , A61K33/06 , A61K33/16 , A61K31/405
摘要: The present invention provides marine protein hydrolysates for use in nutraceuticals, functional foods, foods, beverages, and animal feeds.
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公开(公告)号:EP3500252B1
公开(公告)日:2022-11-02
申请号:EP17757821.8
申请日:2017-08-16
IPC分类号: A61K31/165 , A61K31/401 , A61K31/4045 , A61K38/06 , A61P25/28 , A61P25/00 , A61P25/14 , A61P25/16 , A61P25/18
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10.
公开(公告)号:EP4066895A1
公开(公告)日:2022-10-05
申请号:EP20892362.3
申请日:2020-11-27
发明人: IWAKI, Yuzo , ENDO, Toshimitsu , KUSUMI, Kensuke
IPC分类号: A61P7/00 , A61P43/00 , C07D207/34 , C07D409/04 , C07D409/12 , C07D471/04 , C07D495/04 , C07D513/04 , C07D209/42 , C07D209/52 , A61K31/401 , A61K31/403 , A61K31/4045 , A61K31/407 , A61K31/429 , A61K31/437
摘要: An object of the present invention is to provide a pharmaceutical containing a compound having an agonist activity for LPA3 as an active ingredient. As a result of intensive studies, the inventors of the present invention have found a compound represented by the following general formula (IY):
wherein all symbols represent the same meaning as described in the specification, having an agonist activity for LPA3, as a substance capable of solving such a problem and the like, and completed the present invention. Since the compound represented by general formula (IY) of the present invention and the like have an agonist activity for LPA3, it can be used as an active ingredient of a preventive and/or therapeutic agent for essential thrombocythemia or reactive thrombocytosis.
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