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公开(公告)号:US20160339023A1
公开(公告)日:2016-11-24
申请号:US15107232
申请日:2014-12-19
Applicant: Fang Li , Hui-Qin WANG , Ensar HALILOVIC , Jinsheng LIANG
Inventor: Fang Li , Hui-Qin WANG , Ensar HALILOVIC , Jinsheng LIANG
IPC: A61K31/506 , A61K31/496
CPC classification number: A61K31/506 , A61K31/4025 , A61K31/404 , A61K31/435 , A61K31/496 , A61K45/06 , A61K2300/00
Abstract: A pharmaceutical combination comprising (a) an ALK inhibitor, or a pharmaceutically acceptable salt thereof, and (b) at least one HDMA-2/p53 receptor inhibitor or a pharmaceutically acceptable salt, or at least one BRaf inhibitor or a pharmaceutically acceptable salt, and optionally a pharmaceutically acceptable carrier, for simultaneous, separate or sequential administration; the uses of such combination in the treatment of cancer; and methods of treating a subject suffering from a proliferative disease comprising administering a therapeutically effective amount of such combination.
Abstract translation: 一种药物组合,其包含(a)ALK抑制剂或其药学上可接受的盐,和(b)至少一种HDMA-2 / p53受体抑制剂或其药学上可接受的盐,或至少一种BRaf抑制剂或药学上可接受的盐, 和任选的药学上可接受的载体,用于同时,分别或连续施用; 这种组合在治疗癌症中的用途; 以及治疗患有增殖性疾病的受试者的方法,包括施用治疗有效量的这种组合。
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公开(公告)号:US20160331751A1
公开(公告)日:2016-11-17
申请号:US15106886
申请日:2014-12-19
Applicant: Stephane Ferretti , Sebastien Jeay , Ensar Halilovic , Fang Li , Hui-Qin Wang
Inventor: Stephane Ferretti , Sebastien Jeay , Ensar Halilovic , Fang Li , Hui-Qin Wang
IPC: A61K31/519 , A61K31/506 , A61K31/496
CPC classification number: A61K31/519 , A61K31/4188 , A61K31/496 , A61K31/505 , A61K31/506 , A61K2300/00
Abstract: The disclosure relates to a pharmaceutical combination of a mdm2/4 inhibitor, namely (S)-1-(4-Chloro-phenyl)-7-isopropoxy-6-methoxy-2-(4-{methyl-[4-(4-methyl-3-oxo-piperazin-1-yl)-trans-cyclohexylmethyl]-amino}-phenyl)-1,4-dihydro-2H-isoquinolin-3-one or (S)-5-(5-Chloro-1-methyl-2-oxo-1,2-dihydro-pyridin-3-yl)-6-(4-chloro-phenyl)-2-(2,4-dimethoxy-pyrimidin-5-yl)-1-isopropyl-5,6-dihydro-1H-pyrrolo[3,4-d]imidazol-4-one, and a cyclin dependent kinase 4/6 (CDK4/6) inhibitor 7-Cyclopentyl-2-(5-piperazin-1-yl-pyridin-2-ylamino)-7H-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid dimethylamide. In addition, the disclosure relates to a pharmaceutical combination product. The disclosure also relates to corresponding pharmaceutical formulations, uses and treatment methods comprising said mdm2/4 inhibitor or a cyclin dependent kinase 4/6 (CDK4/6) inhibitor.
Abstract translation: 本公开涉及mdm2 / 4抑制剂的药物组合,即(S)-1-(4-氯 - 苯基)-7-异丙氧基-6-甲氧基-2-(4- {甲基 - [4-(4 - 甲基-3-氧代 - 哌嗪-1-基) - 反式 - 环己基甲基] - 氨基} - 苯基)-1,4-二氢-2H-异喹啉-3-酮或(S)-5-(5-氯 - -1-甲基-2-氧代-1,2-二氢 - 吡啶-3-基)-6-(4-氯 - 苯基)-2-(2,4-二甲氧基 - 嘧啶-5-基)-1-异丙基 -5,6-二氢-1H-吡咯并[3,4-d]咪唑-4-酮和细胞周期蛋白依赖性激酶4/6(CDK4 / 6)抑制剂7-环戊基-2-(5-哌嗪-1-基) 吡啶-2-基氨基)-7H-吡咯并[2,3-d]嘧啶-6-甲酸二甲基酰胺。 此外,本公开涉及药物组合产品。 本公开还涉及包含所述mdm2 / 4抑制剂或细胞周期蛋白依赖性激酶4/6(CDK4 / 6)抑制剂的相应药物制剂,用途和治疗方法。
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