发明名称 Combination therapy
摘要 The present invention relates to a pharmaceutical combination comprising an alpha-isoform specific phosphatidylinositol 3-kinase inhibitor compound, such as (S)-Pyrrolidine-1,2-dicarboxylic acid 2-amide 1-({4-methyl-5-[2-(2,2,2-trifluoro-1,1-dimethyl-ethyl)-pyridin-4-yl]-thiazol-2-yl}-amide), or pharmaceutically acceptable salt thereof, and an insulin-like growth factor-1 receptor (IGF1R) inhibitor (e.g., the IGF1R inhibitor ANTIBODY A, or a variant or derivative thereof), a pharmaceutical composition comprising such combination, methods for treating cancer comprising administration of therapeutically effective amounts of such inhibitors to a subject in need thereof, and uses of such combination for the treatment of cancer.
申请公布号 US8980259(B2) 申请公布日期 2015.03.17
申请号 US201313799076 申请日期 2013.03.13
申请人 Novartis AG;Amgen, Inc. 发明人 Huang Xizhong;Peters Malte;Schumacher Karl Maria;Cao Zhu Alexander;Gansert Jennifer Lorraine;Chang David Dong Eun
分类号 A61K31/4439;A61K39/395;C07K16/28;A61K39/00 主分类号 A61K31/4439
代理机构 Lathrop & Gage LLP 代理人 Lathrop & Gage LLP ;Trinque Brian C.
主权项 1. A method for treating cancer in a subject in need thereof comprising administering to the subject a therapeutically effective amount of: a) the alpha-isoform specific phosphatidylinositol 3-kinase (PI3K) inhibitor (S)-Pyrrolidine-1,2-dicarboxylic acid 2-amide 1-({4-methyl-5-[2-(2,2,2-trifluoro-1,1-dimethyl-ethyl)-pyridin-4-yl]-thiazol-2-yl}-amide) (COMPOUND A) or a pharmaceutically acceptable salt thereof; and b) an insulin-like growth factor-1 receptor (IGF1R) inhibitor which is an antibody comprising a heavy chain and a light chain, wherein the heavy chain comprises a variable region comprising the complementarity determining region (CDR) amino acid sequences set forth in SEQ ID NOs: 5, 6, and 7, and wherein the light chain comprises a variable region comprising the CDR amino acid sequences set forth in SEQ ID NOs: 8, 9, and 10; and wherein the cancer is ovarian cancer or breast cancer.
地址 Basel CH