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公开(公告)号:US20240109972A1
公开(公告)日:2024-04-04
申请号:US18038818
申请日:2021-12-07
Applicant: Genmab A/S , BioNTech SE
Inventor: Ugur SAHIN , Alexander MUIK , Ulf FORSSMANN , Maria JURE-KUNKEL , Manish GUPTA , Tahamtan AHMADI , Kathy AMIRI , Gaurav BAJAJ
IPC: C07K16/28 , A61K31/337 , A61K45/06 , A61P35/00
CPC classification number: C07K16/2878 , A61K31/337 , A61K45/06 , A61P35/00 , C07K16/2827 , A61K2039/505
Abstract: The present invention provides combination therapy to reduce or prevent progression of a tumor or treating cancer in a subject. The combination therapy comprises administration of a binding agent that binds to human CD137 and to human PD-L1; and a taxane chemotherapeutic agent.
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公开(公告)号:US20190233522A1
公开(公告)日:2019-08-01
申请号:US16316000
申请日:2017-07-07
Applicant: GENMAB A/S
Inventor: Ulf FORSSMANN , Steen LISBY , Nedjad LOSIC
CPC classification number: C07K16/2863 , A61K47/6803 , A61K47/6849 , A61K47/6851 , A61K2039/505 , A61P35/00 , C07K2317/33 , C07K2317/34 , C07K2317/56 , C07K2317/732 , C07K2317/77 , C07K2317/92
Abstract: An antibody-drug conjugate (ADC) based on an antibody binding to human AXL and pharmaceutical compositions comprising the ADC for use in the treatment of a cancer comprising administering to a subject a weekly dose of from about 0.45 mg/kg to about 2.0 mg/kg of the ADC once a week for three consecutive weeks followed by a one week resting period without any administration of the ADC so that each cycle time is 28 days including the resting period.
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公开(公告)号:US20230087164A1
公开(公告)日:2023-03-23
申请号:US17795318
申请日:2021-02-04
Applicant: GENMAB A/S , BIONTECH SE
Inventor: Ugur SAHIN , Alexander MUIK , Isil ALTINTAS , Ulf FORSSMANN , Kate SASSER , Maria JURE-KUNKEL , Manish GUPTA
Abstract: The present invention relates to a method for reducing or preventing progression of a tumor or treating cancer. The method comprises administering to a subject, a binding agent comprising a first binding region binding to human CD137 and a second binding region binding to human PD-L1. The amount of binding agent administered in each treatment cycle is preferably about 0.3-5 mg/kg body weight or about 25-400 mg in total.
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公开(公告)号:US20220273809A1
公开(公告)日:2022-09-01
申请号:US17628382
申请日:2020-07-17
Applicant: GENMAB A/S
Inventor: Maarten JANMAAT , Nora PENCHEVA , Esther Cornelia Wilhelmina BREIJ , Julia BOSHUIZEN , Daniel Simon PEEPER , Ulf FORSSMANN , Tahamtan AHMADI , Patricia Garrido CASTRO
Abstract: The present invention relates to conjugates of antibodies and cytotoxic agents for use in treatment of cancer in combination with an inhibitor of PD-1 or PD-L1. The antibodies are directed against Axl.
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公开(公告)号:US20240262924A1
公开(公告)日:2024-08-08
申请号:US18570257
申请日:2022-06-20
Applicant: GENMAB A/S , BioNTech SE
Inventor: Ugur SAHIN , Alexander MUIK , Ulf FORSSMANN , Maria N. JURE-KUNKEL , Gaurav BAJAJ , Craig THALHAUSER , Nora PENCHEVA
CPC classification number: C07K16/2878 , A61P35/00 , C07K16/2827 , A61K2039/505 , A61K2039/54 , A61K2039/545 , C07K2317/31
Abstract: The present invention relates to a method for reducing or preventing progression of a tumor or treating cancer in a subject, comprising administering to the subject a binding agent comprising a first antigen-binding region binding to human CD137, and a second antigen-binding region binding to human PD-L1. The invention further provides a binding agent for use in reducing or preventing progression of a tumor or for use in treatment of cancer.
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公开(公告)号:US20210393793A1
公开(公告)日:2021-12-23
申请号:US17279359
申请日:2019-09-26
Applicant: GENMAB A/S
Inventor: Esther BREIJ , Ulf FORSSMANN , Tahamtan AHMADI
Abstract: The present invention relates to immunoconjugates anti-AXL antibodies and compositions for treatment of non-small cell lung cancer.
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公开(公告)号:US20210070869A1
公开(公告)日:2021-03-11
申请号:US17046199
申请日:2019-04-10
Applicant: GENMAB A/S
Inventor: Maarten JANMAAT , Esther BREIJ , Ulf FORSSMANN , Tahamtan AHMADI , Julia BOSHUIZEN , Daniel PEEPER , Nora PENCHEVA
Abstract: The disclosure relates to anti-AXL antibodies, immunoconjugates, and compositions for treatment of cancer, which is resistant to or is predicted to be or become resistant to treatment with a programmed cell death-1/programmed cell death-1 ligand (PD-1/PD-L1) inhibitor.
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