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公开(公告)号:US20230046904A1
公开(公告)日:2023-02-16
申请号:US17761097
申请日:2020-09-17
Inventor: Yuguang WANG , Feilan WANG , Nong ZHANG
IPC: A61K31/198 , A61K39/395 , A61K45/06
Abstract: The invention provides methods for treating a cancer, comprising administering to a subject in need thereof a therapeutically effective amount of a small molecule inhibitor of the PD-1/PD-L1 interaction or a pharmaceutically acceptable salt or prodrug thereof in combination with a therapeutically effective amount of an anti-PD-1 antibody, wherein the small molecule inhibitor of the PD-1/PD-L1 interaction is not a protein.
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公开(公告)号:US20230192653A1
公开(公告)日:2023-06-22
申请号:US17911053
申请日:2021-03-08
Inventor: Yuguang WANG , Zhenhua FENG , Feilan WANG
IPC: C07D401/14 , C07K16/28 , A61P35/00
CPC classification number: C07D401/14 , C07K16/2896 , A61P35/00 , C07B2200/13
Abstract: The disclosure provides new therapeutic uses for certain fused ring pyrimidine compounds, in particular for treating patients having a cancer which expresses elevated fibroblast growth factor receptor oncogene partner 2 (FGFR1OP2) and/or elevated FGFR1, or expresses a FGFR1-FGFR1OP2 fusion protein, and for treating patients who are being treated with an immune checkpoint inhibitor.
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公开(公告)号:US20220313626A1
公开(公告)日:2022-10-06
申请号:US17621576
申请日:2020-06-23
Inventor: Yugang WANG , Feilan WANG , Nong ZHANG
IPC: A61K31/137 , A61K31/198 , A61K31/357 , A61K31/277 , A61K31/397 , A61K31/401 , A61K31/454 , A61K31/4196 , A61K31/4025 , A61K31/423 , A61K31/4545 , A61P35/02
Abstract: Provided herein are methods for treating a cancer in a subject having a tumor with interstitial fluid pressure (IFP) of at least 10 mmHg, comprising administering to the subject a therapeutically effective amount of a compound or a pharmaceutically acceptable salt or prodrug thereof, which is an inhibitor of the interaction between the PD-1 receptor and its ligand PD-L1 and which is not a protein, alone, or in combination with other agents, e.g., in combination with the use of anti-PD-1/PD-L1 antibodies, in combination with an inhibitor of the CTLA-4/B7 interaction, or in combination with an inhibitor binding to VEFG.
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