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公开(公告)号:US09295669B2
公开(公告)日:2016-03-29
申请号:US13313042
申请日:2011-12-07
申请人: Kapil Dhingra , Brian Higgins , Kenneth Kolinsky , Richard J. Lee , Brian Lestini , Kathryn Packman , Fei Su
发明人: Kapil Dhingra , Brian Higgins , Kenneth Kolinsky , Richard J. Lee , Brian Lestini , Kathryn Packman , Fei Su
IPC分类号: A61K31/535 , A61K31/505 , A61K38/21 , A01N43/54 , A01N43/42 , C07D413/00 , C07D239/02 , C07D401/00 , C07D403/00 , C07D471/02 , A61K31/437
CPC分类号: A61K38/212 , A61K31/437 , A61K38/21 , A61K2300/00
摘要: The present invention relates to a combination therapy of propane-1-sulfonic acid{3-[5-(4-chloro-phenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl-2,4-difluoro-phenyl]-amide}, or a pharmaceutically acceptable salt thereof, and an interferon for treating a patient suffering from a proliferative disorder, in particular a solid tumor, for example, colorectal cancer, melanoma, and thyroid cancer. In particular, the present invention relates to such a therapy wherein the interferon is peginterferon alfa-2a and the disorder is melanoma containing the V600E b-Raf mutation.
摘要翻译: 本发明涉及丙烷-1-磺酸{3- [5-(4-氯 - 苯基)-1H-吡咯并[2,3-b]吡啶-3-羰基-2,4-二氟 - 苯基] - 酰胺}或其药学上可接受的盐,以及用于治疗患有增殖性疾病,特别是实体瘤例如结肠直肠癌,黑素瘤和甲状腺癌的患者的干扰素。 特别地,本发明涉及这样的治疗,其中干扰素是聚乙二醇化干扰素α-2a,该病症是含有V600E b-Raf突变的黑素瘤。
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公开(公告)号:US20120045433A1
公开(公告)日:2012-02-23
申请号:US13206548
申请日:2011-08-10
申请人: Kapil Dhingra , Brian Higgins , Kenneth Kolinsky , Richard J. Lee , Brian Lestini , Kathryn Packman , Fei Su
发明人: Kapil Dhingra , Brian Higgins , Kenneth Kolinsky , Richard J. Lee , Brian Lestini , Kathryn Packman , Fei Su
IPC分类号: A61K31/437 , A61K39/395 , A61P35/00 , A61K31/4545
CPC分类号: A61K31/00 , A61K31/437 , A61K31/4745 , A61K39/39558 , A61K45/06 , A61K2039/545 , C07K16/2863 , A61K2300/00
摘要: The present invention relates to a combination therapy of propane-1-sulfonic acid {3-[5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-2,4-difluoro-phenyl}-amide, or a pharmaceutically acceptable salt thereof, and an topoisomerase inhibitor for treating a patient suffering from a proliferative disorder, in particular a solid tumor, for example, colorectal cancer, melanoma, and thyroid cancer. In particular, the present invention relates to such a therapy wherein the topoisomerase inhibitor is irinotecan, or a pharmaceutically acceptable salt thereof, and the disorder is colorectal cancer involving a tumor comprising b-Raf having the V600E mutation.
摘要翻译: 本发明涉及丙烷-1-磺酸{3- [5-(4-氯苯基)-1H-吡咯并[2,3-b]吡啶-3-羰基] -2,4-二氟 - 苯基} - 酰胺或其药学上可接受的盐,和拓扑异构酶抑制剂,用于治疗患有增殖性病症的患者,特别是实体瘤,例如结肠直肠癌,黑素瘤和甲状腺癌。 特别地,本发明涉及这样的治疗方法,其中拓扑异构酶抑制剂是伊立替康或其药学上可接受的盐,该病症是涉及包含具有V600E突变的b-Raf的肿瘤的结肠直肠癌。
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公开(公告)号:US06548531B2
公开(公告)日:2003-04-15
申请号:US10055451
申请日:2002-01-23
IPC分类号: A61R31405
CPC分类号: A61K31/337 , A61K31/404 , A61K31/40 , A61K31/335 , A61K2300/00
摘要: Disclosed is a method of treating a patient suffering from cancer. The method comprises administering to a patient over a period of up to about 15 days a first component and a second component. The first component consists of a pharmaceutical composition containing as an active ingredient a compound of formula I or a pharmaceutically acceptable salt or ester of said compound. The second component consists of an injection solution containing as an active ingredient paclitaxel. The amount of each component in the combination is such that the combination is therapeutically effective. The components are administered concomitantly or sequentially in a three week to four week treatment cycle for as long as the tumor remains under control and the patient tolerates the regimen.
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公开(公告)号:US08709419B2
公开(公告)日:2014-04-29
申请号:US13206557
申请日:2011-08-10
申请人: Kapil Dhingra , Brian Higgins , Kenneth Kolinsky , Richard J. Lee , Brian Lestini , Kathryn Packman , Fei Su
发明人: Kapil Dhingra , Brian Higgins , Kenneth Kolinsky , Richard J. Lee , Brian Lestini , Kathryn Packman , Fei Su
IPC分类号: A61K39/00 , A61K31/517 , A61K31/44
CPC分类号: A61K31/4745 , A61K31/00 , A61K31/437 , A61K31/517 , A61K39/395 , A61K45/06 , A61K2039/505 , C07K16/2863 , C07K2317/24 , C07K2317/76 , A61K2300/00
摘要: The present invention relates to a combination therapy of propane-1-sulfonic acid {3-[5-(4-chloro-phenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-2,4-difluoro-phenyl}-amide, or a pharmaceutically acceptable salt thereof, and an EGFR inhibitor for treating a patient suffering from a proliferative disorder, in particular a solid tumor, for example, colorectal cancer, melanoma, and thyroid cancer.
摘要翻译: 本发明涉及丙烷-1-磺酸{3- [5-(4-氯 - 苯基)-1H-吡咯并[2,3-b]吡啶-3-羰基] 二氟 - 苯基} - 酰胺或其药学上可接受的盐,以及用于治疗患有增殖性病症的患者,特别是实体瘤例如结肠直肠癌,黑素瘤和甲状腺癌的EGFR抑制剂。
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公开(公告)号:US20120148533A1
公开(公告)日:2012-06-14
申请号:US13313042
申请日:2011-12-07
申请人: Kapil Dhingra , Brian Higgins , Kenneth Kolinsky , Richard J. Lee , Brian Lestini , Kathryn Packman , Fei Su
发明人: Kapil Dhingra , Brian Higgins , Kenneth Kolinsky , Richard J. Lee , Brian Lestini , Kathryn Packman , Fei Su
CPC分类号: A61K38/212 , A61K31/437 , A61K38/21 , A61K2300/00
摘要: The present invention relates to a combination therapy of propane-1-sulfonic acid{3-[5-(4-chloro-phenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl-2,4-difluoro-phenyl]-amide}, or a pharmaceutically acceptable salt thereof, and an interferon for treating a patient suffering from a proliferative disorder, in particular a solid tumor, for example, colorectal cancer, melanoma, and thyroid cancer. In particular, the present invention relates to such a therapy wherein the interferon is peginterferon alfa-2a and the disorder is melanoma containing the V600E b-Raf mutation.
摘要翻译: 本发明涉及丙烷-1-磺酸{3- [5-(4-氯 - 苯基)-1H-吡咯并[2,3-b]吡啶-3-羰基-2,4-二氟 - 苯基] - 酰胺}或其药学上可接受的盐,以及用于治疗患有增殖性疾病,特别是实体瘤例如结肠直肠癌,黑素瘤和甲状腺癌的患者的干扰素。 特别地,本发明涉及这样的治疗,其中干扰素是聚乙二醇化干扰素α-2a,该病症是含有V600E b-Raf突变的黑素瘤。
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公开(公告)号:US20120045434A1
公开(公告)日:2012-02-23
申请号:US13206557
申请日:2011-08-10
申请人: Kapil Dhingra , Brian Higgins , Kenneth Kolinsky , Richard J. Lee , Brian Lestini , Kathryn Packman , Fei Su
发明人: Kapil Dhingra , Brian Higgins , Kenneth Kolinsky , Richard J. Lee , Brian Lestini , Kathryn Packman , Fei Su
IPC分类号: A61K39/395 , A61P35/00 , A61K31/4738 , A61K31/437 , A61K31/517
CPC分类号: A61K31/4745 , A61K31/00 , A61K31/437 , A61K31/517 , A61K39/395 , A61K45/06 , A61K2039/505 , C07K16/2863 , C07K2317/24 , C07K2317/76 , A61K2300/00
摘要: The present invention relates to a combination therapy of propane-1-sulfonic acid {3-[5-(4-chloro-phenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-2,4-difluoro-phenyl}-amide, or a pharmaceutically acceptable salt thereof, and an EGFR inhibitor for treating a patient suffering from a proliferative disorder, in particular a solid tumor, for example, colorectal cancer, melanoma, and thyroid cancer.
摘要翻译: 本发明涉及丙烷-1-磺酸{3- [5-(4-氯 - 苯基)-1H-吡咯并[2,3-b]吡啶-3-羰基] 二氟 - 苯基} - 酰胺或其药学上可接受的盐,以及用于治疗患有增殖性病症的患者,特别是实体瘤例如结肠直肠癌,黑素瘤和甲状腺癌的EGFR抑制剂。
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