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公开(公告)号:US5919763A
公开(公告)日:1999-07-06
申请号:US87796
申请日:1998-06-01
申请人: Eithan Galun , Stefan Rose-John , Malte Peters
发明人: Eithan Galun , Stefan Rose-John , Malte Peters
IPC分类号: A61K45/00 , A61K38/00 , A61K38/20 , A61K48/00 , A61P1/16 , A61P31/12 , C07K14/54 , C07K14/715 , C12N15/62
CPC分类号: A61K38/204 , Y10S514/893 , Y10S514/894
摘要: A method for treating an injury of a liver of a subject with a composition featuring a pharmaceutically acceptable amount of an IL-6/sIL-6R complex, preferably Hyper-IL-6. The composition is administered to the subject such that the injury to the liver is treated.
摘要翻译: 一种以具有药学上可接受量的IL-6 / sIL-6R复合物,优选Hyper-IL-6为特征的组合物治疗受试者肝损伤的方法。 将组合物施用于受试者,使得对肝脏的损伤进行治疗。
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公开(公告)号:US20130273061A1
公开(公告)日:2013-10-17
申请号:US13799706
申请日:2013-03-13
申请人: Xizhong Huang , Malte Peters , Jennifer Lorraine Gansert , David Dong Eun Chang , Pedro Beltran
发明人: Xizhong Huang , Malte Peters , Jennifer Lorraine Gansert , David Dong Eun Chang , Pedro Beltran
IPC分类号: A61K39/395 , A61K31/4184
CPC分类号: A61K39/3955 , A61K31/4184 , A61K2039/545 , C07K16/2863 , A61K2300/00
摘要: The present invention relates to a pharmaceutical combination comprising a MEK inhibitor compound 6-(4-bromo-2-fluorophenylamino)-7-fluoro-3-methyl-3H-benzoimidazole-5-carboxylic acid (2-hydroxyethyoxy)-amide or a pharmaceutically acceptable salt thereof and the IGF1R inhibitor ANTIBODY A, a pharmaceutical composition comprising such combination, methods for treating cancer comprising administration of a therapeutically effective amount of such combination to a subject in need thereof, and uses of such combination for the treatment of cancer.
摘要翻译: 本发明涉及药物组合,其包含MEK抑制剂化合物6-(4-溴-2-氟苯基氨基)-7-氟-3-甲基-3H-苯并咪唑-5-甲酸(2-羟基乙氧基) - 酰胺或 其药学上可接受的盐和IGF1R抑制剂抗体A,包含这种组合的药物组合物,用于治疗癌症的方法,包括向有需要的受试者施用治疗有效量的这种组合,以及这种组合用于治疗癌症的用途。
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公开(公告)号:US20170304443A1
公开(公告)日:2017-10-26
申请号:US15510414
申请日:2015-09-11
申请人: David Lebwohl , Malte Peters , NOVARTIS AG
发明人: David Lebwohl , Malte Peters
IPC分类号: A61K39/395 , A61K31/55 , A61K39/00
CPC分类号: A61K39/39558 , A61K9/0053 , A61K31/506 , A61K31/55 , A61K2039/505 , A61K2039/54 , A61K2039/542 , A61K2039/545 , C07K16/28 , C07K16/2803 , C07K16/2818 , C07K16/2827 , C07K16/3023 , C07K2317/21 , C07K2317/76 , A61K2300/00
摘要: Combination therapies are disclosed. The combination therapies can be used to treat or prevent cancerous conditions and/or disorders.
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公开(公告)号:US20170296659A1
公开(公告)日:2017-10-19
申请号:US15510355
申请日:2015-09-11
申请人: David Lebwohl , Malte Peters , Novartis AG
发明人: David Lebwohl , Malte Peters
IPC分类号: A61K39/395 , C07K16/28
摘要: Disclosed is a combination comprising an immunomodulator and a second therapeutic agent for use in treating cancer, wherein the immunomodulator is an inhibitor of an immune checkpoint molecule or an activator of a costimulatory molecule, or a combination thereof; and the second therapeutic agent is chosen from one or more of: 1) a c-MET inhibitor; 2) a CDK4/6 inhibitor; 3) a PI3K inhibitor; 4) a BRAF inhibitor; 5) an FGFR inhibitor; 6) a MEK inhibitor, or 7) a BCR-ABL inhibitor. The combination therapies can be used to treat or prevent cancerous conditions and/or disorders.
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公开(公告)号:US08980259B2
公开(公告)日:2015-03-17
申请号:US13799076
申请日:2013-03-13
申请人: Xizhong Huang , Malte Peters , Karl Maria Schumacher , Zhu Alexander Cao , Jennifer Lorraine Gansert , David Dong Eun Chang
发明人: Xizhong Huang , Malte Peters , Karl Maria Schumacher , Zhu Alexander Cao , Jennifer Lorraine Gansert , David Dong Eun Chang
IPC分类号: A61K31/4439 , A61K39/395 , C07K16/28 , A61K39/00
CPC分类号: A61K31/4439 , A61K39/3955 , A61K2039/505 , C07K16/2863 , C07K2316/96 , C07K2317/565 , C07K2317/73 , C07K2317/76 , A61K2300/00
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.
摘要翻译: 本发明涉及药物组合,其包含α-异构体特异性磷脂酰肌醇3-激酶抑制剂化合物,例如(S) - 吡咯烷-1,2-二羧酸2-酰胺1 - ({4-甲基-5- [2 - (2,2,2-三氟-1,1-二甲基 - 乙基) - 吡啶-4-基] - 噻唑-2-基} - 酰胺)或其药学上可接受的盐,以及胰岛素样生长因子 - 1受体(IGF1R)抑制剂(例如,IGF1R抑制剂抗体A或其变体或衍生物),包含这种组合的药物组合物,用于治疗癌症的方法,包括向有需要的受试者施用治疗有效量的此类抑制剂, 以及这种组合用于治疗癌症的用途。
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公开(公告)号:US20120294873A1
公开(公告)日:2012-11-22
申请号:US13486749
申请日:2012-06-01
申请人: Malte Peters , Mathias Locher , Nadja Prang , Cornelia Quadt
发明人: Malte Peters , Mathias Locher , Nadja Prang , Cornelia Quadt
IPC分类号: A61K39/395 , C07K16/30 , A61P35/00
CPC分类号: C07K16/30 , A61K2039/505 , C07K2317/21
摘要: The invention relates inter alia to a method of treating tumorous disease in a human patient by administering to the patient a human immunoglobulin specifically binding to the human EpCAM antigen, the immunoglobulin exhibiting a serum half-life of at least 15 days, the method comprising the step of administering the immunoglobulin no more frequently than once every week, preferably no more frequently than once every two weeks.
摘要翻译: 本发明特别涉及通过向患者施用与人EpCAM抗原特异性结合的人免疫球蛋白,该免疫球蛋白的血清半衰期至少为15天,该方法包括: 每周施用免疫球蛋白的步骤不超过一次,优选不超过每两周一次。
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公开(公告)号:US20070274982A1
公开(公告)日:2007-11-29
申请号:US10589450
申请日:2005-02-09
申请人: Malte Peters , Mathias Locher , Nadja Prang , Cornelia Quadt
发明人: Malte Peters , Mathias Locher , Nadja Prang , Cornelia Quadt
IPC分类号: A61K39/395 , A61P35/00 , C07K16/30
CPC分类号: C07K16/30 , A61K2039/505 , C07K2317/21
摘要: The invention relates inter alia to a method of treating tumorous disease in a human patient by administering to the patient a human immunoglobulin specifically binding to the human EpCAM antigen, the immunoglobulin exhibiting a serum half-life of at least 15 days, the method comprising the step of administering the immunoglobulin no more frequently than once every week, preferably no more frequently than once every two weeks.
摘要翻译: 本发明特别涉及通过向患者施用与人EpCAM抗原特异性结合的人免疫球蛋白,该免疫球蛋白的血清半衰期至少为15天,该方法包括: 每周施用免疫球蛋白的步骤不超过一次,优选不超过每两周一次。
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公开(公告)号:US20050180979A1
公开(公告)日:2005-08-18
申请号:US10778915
申请日:2004-02-13
申请人: Malte Peters , Mathias Locher , Nadja Prang , Cornelia Quadt
发明人: Malte Peters , Mathias Locher , Nadja Prang , Cornelia Quadt
IPC分类号: C07K16/30 , G01N33/574 , A61K39/395
CPC分类号: C07K16/30 , A61K2039/505 , C07K2317/21
摘要: The invention relates inter alia to a method of treating tumorous disease in a human patient by administering to the patient a human immunoglobulin specifically binding to the human EpCAM antigen, the immunoglobulin exhibiting a serum half-life of at least 15 days, the method comprising the step of administering the immunoglobulin no more frequently than once every week, preferably no more frequently than once every two weeks.
摘要翻译: 本发明特别涉及通过向患者施用与人EpCAM抗原特异性结合的人免疫球蛋白,该免疫球蛋白的血清半衰期至少为15天,该方法包括: 每周施用免疫球蛋白的步骤不超过一次,优选不超过每两周一次。
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公开(公告)号:US08961970B2
公开(公告)日:2015-02-24
申请号:US13799706
申请日:2013-03-13
申请人: Xizhong Huang , Malte Peters , Jennifer Lorraine Gansert , David Dong Eun Chang , Pedro Beltran , Zhu Alexander Cao
发明人: Xizhong Huang , Malte Peters , Jennifer Lorraine Gansert , David Dong Eun Chang , Pedro Beltran , Zhu Alexander Cao
IPC分类号: A61K39/395 , C07K16/28 , A61K31/4184 , A61K39/00
CPC分类号: A61K39/3955 , A61K31/4184 , A61K2039/545 , C07K16/2863 , A61K2300/00
摘要: The present invention relates to a pharmaceutical combination comprising a MEK inhibitor compound 6-(4-bromo-2-fluorophenylamino)-7-fluoro-3-methyl-3H-benzoimidazole-5-carboxylic acid (2-hydroxyethyoxy)-amide or a pharmaceutically acceptable salt thereof and the IGF1R inhibitor ANTIBODY A, a pharmaceutical composition comprising such combination, methods for treating cancer comprising administration of a therapeutically effective amount of such combination to a subject in need thereof, and uses of such combination for the treatment of cancer.
摘要翻译: 本发明涉及药物组合,其包含MEK抑制剂化合物6-(4-溴-2-氟苯基氨基)-7-氟-3-甲基-3H-苯并咪唑-5-甲酸(2-羟基乙氧基) - 酰胺或 其药学上可接受的盐和IGF1R抑制剂抗体A,包含这种组合的药物组合物,用于治疗癌症的方法,包括向有需要的受试者施用治疗有效量的这种组合,以及这种组合用于治疗癌症的用途。
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