发明公开
EP1418917A1 USE OF C-SRC INHIBITORS ALONE OR IN COMBINATION WITH STI571 FOR THE TREATMENT OF LEUKAEMIA
审中-公开
c-SRC USE单独或组合性抑制剂STI571 FOR白血病的治疗
- 专利标题: USE OF C-SRC INHIBITORS ALONE OR IN COMBINATION WITH STI571 FOR THE TREATMENT OF LEUKAEMIA
- 专利标题(中): c-SRC USE单独或组合性抑制剂STI571 FOR白血病的治疗
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申请号: EP02794592.2申请日: 2002-08-09
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公开(公告)号: EP1418917A1公开(公告)日: 2004-05-19
- 发明人: DONATO, Nicholas, J. , FABBRO, Doriano , MANLEY, Paul, William , MESTAN, Jürgen , WARMUTH, Markus , HALLEK, Michael , TALPAZ, Moshe , WU, Ji
- 申请人: Novartis AG , GSF - National Research Institute for Environment and Health, GmbH , GSF - Forschungszentrum für Umwelt und Gesundheit GmbH , BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM
- 申请人地址: Lichtstrasse 35 4056 Basel CH
- 专利权人: Novartis AG,GSF - National Research Institute for Environment and Health, GmbH,GSF - Forschungszentrum für Umwelt und Gesundheit GmbH,BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM
- 当前专利权人: Novartis AG,GSF - National Research Institute for Environment and Health, GmbH,GSF - Forschungszentrum für Umwelt und Gesundheit GmbH,BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM
- 当前专利权人地址: Lichtstrasse 35 4056 Basel CH
- 代理机构: Grubb, Philip William
- 优先权: US311690P 20010810
- 国际公布: WO2003013540 20030220
- 主分类号: A61K31/506
- IPC分类号: A61K31/506 ; A61K31/519 ; A61P35/02
摘要:
The invention relates to a combination which comprises (a) at least one compound decreasing the c-Src activity and (b) N-{5-[4-(4-methyl-piperazino-methyl)-benzoylamido]-2-methylphenyl}-4-(3-pyridyl)-2-pyrimidine-amine or the monomethanesulfonate salt thereof; to pharmaceutical compositions comprising said combinations; and to a method of treating a warm-blooded animal having leukaemia, especially chronic myelogenous leukaemia, comprising administering to the animal at least one compound inhibiting the activity of a member of the Src kinase family, the Btk kinase family, the Tec kinase family or a Raf kinase inhibitor, in particular inhibiting the c-Src protein tyrosine kinase activity or inhibiting simultaneously the c-Src protein tyrosine kinase activity and the Bcr-Abl tyrosine kinase activity, alone or in combination with a Bcr-Abl inhibitor, in particular N-{5-[4-(4-methyl-piperazino-methyl)-benzoylamido]-2-methylphenyl}-4-(3-pyridyl)-2-pyrimidine-amine.
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