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公开(公告)号:US20210363254A1
公开(公告)日:2021-11-25
申请号:US16981828
申请日:2019-03-18
申请人: Novartis AG
发明人: Stephane FERRETTI , Nelson GUERREIRO , Ensar HALILOVIC , Sebastien JEAY , Astrid JULLION , Jinsheng LIANG , Christophe MEILLE , Hui-Qin WANG , Jens WUERTHNER
IPC分类号: C07K16/28 , A61P35/00 , C07D487/04
摘要: The present invention relates to a pharmaceutical combination which comprises (a) at least one antibody molecule (e.g., humanized antibody molecules) that bind to Programmed Death 1 (PD-1), and (b) a HDM2-p53 interaction inhibitor, said combination for simultaneous, separate or sequential administration for use in the treatment of a proliferative disease, a pharmaceutical composition comprising such combination; a method of treating a subject having a proliferative disease comprising administration of said combination to a subject in need thereof; use of such combination for the treatment of proliferative disease; and a commercial package comprising such combination; said proliferative disease being a TP53 wildtype tumor, in particular TP53 wildtype renal cell carcinoma (RCC) or TP53 wildtype colorectal cancer (CRC).
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公开(公告)号:US20230172920A1
公开(公告)日:2023-06-08
申请号:US17996616
申请日:2021-04-19
申请人: Novartis AG
IPC分类号: A61K31/4439 , A61P25/28
CPC分类号: A61K31/4439 , A61P25/28
摘要: The present disclosure relates to the field of pharmacy, particularly to a CSF-1R inhibitor for use in the treatment of disease modulated by CSF-1R. For example, the disclosure relates to a CSF-1R inhibitor for use in the treatment of cancer or neurodegenerative diseases. The disclosure also relates to a CSF-1R inhibitor or a pharmaceutical combination comprising a CSF-1R inhibitor, or a pharmaceutically acceptable salt thereof, and an anti-PD-1 antibody molecule, or a pharmaceutically acceptable salt thereof, for use in the treatment of cancer; to a method for the treatment of cancer that involves administering a CSF-1R inhibitor or the combination; and to the use of a CSF-1R inhibitor or the combination for the manufacture of a medicament for the treatment of cancer.
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公开(公告)号:US20210386763A1
公开(公告)日:2021-12-16
申请号:US17415985
申请日:2019-12-18
申请人: NOVARTIS AG
IPC分类号: A61K31/635 , A61K31/506 , A61K45/06 , A61P35/02
摘要: The present invention relates to the combination of the HDM2-p53 interaction inhibitor drug (S)-5-(5-Chloro-1-methyl-2-oxo-1,2-dihydro-pyridin-3-yl)-6-(4-chloro-phenyl)-2-(2,4-dimethoxy-pyrimidin-5-yl)-1-isopropyl-5,6-dihydro-1H-pyrrolo[3,4-d]imidazol-4-one [HDM201] and the BCL2 inhibitor 4-(4-{[2-(4-chlorophenyl)-4,4-dimethylcyclohex-1-en-1-yl]methyl}piperazin-1-yl)-N-[(3-nitro-4-{[(oxan-4yl)methyl]amino}phenyl)sulfonyl]-2-[(1H-pyrrolo[2,3-b]pyridin-5-yl)oxy]benzamide [venetoclax]. The present invention further relates to the use of said combination in the treatment of cancer, in particular hematological tumors. The present invention further relates to dose and dosing regimen related to this combination cancer treatment.
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公开(公告)号:US20200281925A1
公开(公告)日:2020-09-10
申请号:US16494927
申请日:2018-03-29
申请人: Novartis AG
发明人: Stephane FERRETTI , Nesol GURREIO , Senastien JEAY , Astrid JULLION , Christophe MEILLE , Jens WUERTHNER
IPC分类号: A61K31/506 , A61K45/06 , A61K31/553 , A61K31/706 , A61K31/7068 , A61P35/00
摘要: The present invention relates to the HDM2-p53 interaction inhibitors (S)-5-(5-Chloro-1-methyl-2-oxo-1,2-dihydro-pyridin-3-yl)-6-(4-chloro-phenyl)-2-(2,4-dimethoxy-pyrimidin-5-yl)-1-isopropyl-5,6-dihydro-1H-pyrrolo[3,4-d]imidazol-4-one (HDM201), or a pharmaceutically acceptable non-covalent derivative thereof, for use in the treatment of patients with hematological tumors, wherein the drug is administered by an extended low dose dosing regimen.
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公开(公告)号:US20220031697A1
公开(公告)日:2022-02-03
申请号:US17401600
申请日:2021-08-13
申请人: Novartis AG
发明人: Stephane FERRETTI , Nelson GUERREIRO , Sebastien JEAY , Astrid JULLION , Christophe MEILLE , Jens WUERTHNER , Claire Fabre
IPC分类号: A61K31/506 , A61P35/00 , A61K31/553 , A61K31/706 , A61K31/7068 , A61K45/06
摘要: The present invention relates to the HDM2-p53 interaction inhibitors (S)-5-(5-Chloro-1-methyl-2-oxo-1,2-dihydro-pyridin-3-yl)-6-(4-chloro-phenyl)-2-(2,4-dimethoxy-pyrimidin-5-yl)-1-isopropyl-5,6-dihydro-1H-pyrrolo[3,4-d]imidazol-4-one (HDM201), or a pharmaceutically acceptable non-covalent derivative thereof, for use in the treatment of patients with hematological tumors, wherein the drug is administered by an extended low dose dosing regimen.
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