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公开(公告)号:US12275715B2
公开(公告)日:2025-04-15
申请号:US18506060
申请日:2023-11-09
Applicant: FORMA Therapeutics, Inc.
Inventor: Jian Lin , Anna Ericsson , Ann-Marie Campbell , Gary Gustafson , Zhongguo Wang , R. Bruce Diebold , Susan Ashwell , David R. Lancia, Jr. , Justin Andrew Caravella , Wei Lu
IPC: C07D401/12 , A61P35/00 , C07D401/14 , C07D471/04 , A61K31/47
Abstract: The invention relates to inhibitors of mutant isocitrate dehydrogenase (mt-IDH) proteins with neomorphic activity useful in the treatment of cell-proliferation disorders and cancers, having the Formula: where A, U, W1, W2, W3, R1-R6, and R9 are described herein.
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公开(公告)号:US20240132499A1
公开(公告)日:2024-04-25
申请号:US18476249
申请日:2023-09-27
Applicant: FORMA Therapeutics, Inc.
Inventor: Alex J. Buckmelter , Justin Andrew Caravella , Hongbin Li , Matthew W. Martin , Steven Mischke , David James Richard , Angela V. West
IPC: C07D471/18 , C07D403/12 , C07D471/08 , C07D487/08 , C07D487/18 , C07D491/107
CPC classification number: C07D471/18 , C07D403/12 , C07D471/08 , C07D487/08 , C07D487/18 , C07D491/107
Abstract: The disclosure relates to USP30 Inhibitor Compounds, pharmaceutically acceptable salts thereof, pharmaceutical compositions comprising same, and medical uses involving same.
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公开(公告)号:US20240131011A1
公开(公告)日:2024-04-25
申请号:US18125932
申请日:2023-03-24
Applicant: FORMA Therapeutics, Inc.
Inventor: George P. Luke , Suresh Babu
IPC: A61K31/436 , A61K9/00 , A61K9/20
CPC classification number: A61K31/436 , A61K9/0053 , A61K9/2009 , A61K9/2013 , A61K9/2018 , A61K9/2027 , A61K9/2054
Abstract: The present disclosure provides crystalline solid forms, spray-dried dispersions and pharmaceutical compositions, including solid oral dosage forms, of (S)-1-(5-[2H,3H-[1,4]dioxino[2,3-b]pyridine-7-sulfonyl]-1H,2H,3H,4H,5H,6H-pyrrolo[3,4-c]pyrrol-2-yl)-3-hydroxy-2-phenylpropan-1-one (“Compound 1”), and preparation methods thereof.
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公开(公告)号:US11963956B2
公开(公告)日:2024-04-23
申请号:US17700027
申请日:2022-03-21
Applicant: FORMA Therapeutics, Inc.
Inventor: Patrick F. Kelly , Susan Ashwell , Blythe Thomson , Alan Collis , Jeff Davis , Duncan Walker , Wei Lu
IPC: A61K31/4709 , A61P35/00
CPC classification number: A61K31/4709 , A61P35/00
Abstract: Patients diagnosed with a cancer harboring an IDH-1 mutation can be treated by the administration of a therapeutically effective amount of a pharmaceutical composition comprising Compound 1, a selective inhibitor of 2-HG production from mIDH-1 enzymes including the R132 mutations R132C, R132H, R132L, R132G, and R132S.
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公开(公告)号:US20240033261A1
公开(公告)日:2024-02-01
申请号:US18215727
申请日:2023-06-28
Applicant: FORMA Therapeutics, Inc.
Inventor: George P. Luke , Pratik Sheth
IPC: A61K31/4709 , A61K9/00 , A61K47/12 , A61K47/38
CPC classification number: A61K31/4709 , A61K9/0053 , A61K47/12 , A61K47/38
Abstract: The present disclosure reports solid forms of ((S)-5-((1-(6-chloro-2-oxo-1,2-dihydroquinolin-3-yl)ethyl)amino)-1-methyl-6-oxo-1,6-dihydropyridine-2-carbonitrile.
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公开(公告)号:US11795168B2
公开(公告)日:2023-10-24
申请号:US17482717
申请日:2021-09-23
Applicant: FORMA Therapeutics, Inc.
Inventor: George Luke , Suresh Babu
IPC: C07D471/04 , A61K9/48 , A61K9/16
CPC classification number: C07D471/04 , A61K9/1611 , A61K9/1617 , A61K9/1623 , A61K9/1635 , A61K9/1652 , A61K9/485 , A61K9/4858 , A61K9/4866
Abstract: The present disclosure is directed to solid and salt forms of inhibitors of the CBP/p300 family of bromodomains made up of salts and crystalline forms of Formula (I). The compounds can be useful in the treatment of disease or disorders associated with the inhibition of the CBP/p300 family of bromodomains. For instance, the disclosure is concerned with compounds and compositions for inhibition of the CBP/p300 family of bromodomains, methods of treating diseases or disorders associated with the inhibition of CBP/p300 family of bromodomains (e.g., certain forms of cancer), and methods of synthesis of these compounds.
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公开(公告)号:US20230061891A1
公开(公告)日:2023-03-02
申请号:US17383610
申请日:2021-07-23
Applicant: FORMA Therapeutics, Inc.
Inventor: Kenneth W. Bair , Torsten Herbertz , Goss S. Kauffman , Katherine J. Kayser-Bricker , George P. Luke , Matthew W. Martin , David S. Millan , Shawn E.R. Schiller , Adam C. Talbot
IPC: C07D401/04 , C07D401/14 , A61K31/4709 , A61K45/06 , A61K31/47 , A61K31/497 , A61K31/506 , A61K31/5377 , C07D405/14 , C07D413/14 , C07D215/20 , C07D215/48 , C07D409/14 , C07D413/04 , C07D417/04 , C07D417/14 , C07D471/04 , C07D473/28 , C07D487/04 , A61K31/517 , A61K31/519 , A61K31/496 , A61K31/501 , A61K31/52 , C07D401/12 , C07D405/04 , C07D417/10
Abstract: The present invention relates to inhibitors of bromo and extra terminal (BET) bromodomains that are useful for the treatment of cancer, inflammatory diseases, diabetes, and obesity, having Formula I: wherein W, X, Y, Z, R1, R2, R5, and R8 are as described herein.
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公开(公告)号:US11498913B2
公开(公告)日:2022-11-15
申请号:US17101018
申请日:2020-11-23
Applicant: FORMA Therapeutics, Inc.
Inventor: Jian Lin , Anna Ericsson , Ann-Marie Campbell , Gary Gustafson , Zhongguo Wang , R. Bruce Diebold , Susan Ashwell , David R. Lancia, Jr. , Justin Andrew Caravella , Wei Lu
IPC: C07D401/12 , C07D401/14 , C07D471/04 , A61P35/00 , A61K31/47
Abstract: The invention relates to inhibitors of mutant isocitrate dehydrogenase (mt-IDH) proteins with neomorphic activity useful in the treatment of cell-proliferation disorders and cancers, having the Formula: where A, U, W1, W2, W3, R1-R6, and R9 are described herein.
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公开(公告)号:US11299484B2
公开(公告)日:2022-04-12
申请号:US17021759
申请日:2020-09-15
Applicant: FORMA Therapeutics, Inc.
Inventor: Matthew W. Martin , Mary-Margaret Zablocki , Scot Mente , Christopher Dinsmore , Zhongguo Wang , Xiaozhang Zheng
IPC: C07D405/14 , C07D221/20 , C07D409/14 , C07D413/14 , C07D405/06
Abstract: The present disclosure is directed to inhibitors of FASN. The compounds can be useful in the treatment of disease or disorders associated with the inhibition of FASN. For instance, the disclosure is concerned with compounds and compositions for inhibition of FASN, methods of treating, preventing, or ameliorating diseases or disorders associated with the inhibition of FASN, and methods of synthesis of these compounds.
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公开(公告)号:US20220088005A1
公开(公告)日:2022-03-24
申请号:US17482720
申请日:2021-09-23
Applicant: FORMA Therapeutics, Inc.
Inventor: Sylvie GUICHARD , Maureen CALIGIURI , Anna ERICSSON , Qunli XU , Hesham MOHAMED
IPC: A61K31/4745 , A61P35/00
Abstract: Methods for treating certain androgen receptor-positive forms of cancer using inhibitors of the CREB binding protein bromodomain are disclosed. In some methods, the AR-positive forms of cancer may be breast cancer, including triple negative forms, hormone receptor positive forms, and HER2-positive forms. In other methods, the AR-positive forms of cancer may be prostate cancer, including metastatic castration resistant prostate cancer. In some embodiments, methods of treating prostate cancer comprise the step of administering to a patient in need thereof the compound (1R,3R)-3-[(7S)-2-[(R)-(5-fluoro-2-methoxyphenyl)(hydroxy)methyl]-6-(methoxycarbonyl)-7-methyl-3H,6H,7H,8H,9H-imidazo[4,5-f]quinolin-3-yl]cyclohexane-1-carboxylic acid, or a pharmaceutically acceptable salt thereof.
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