SG11201406468YA - Salt form of a human hi stone methyltransf erase ezh2 inhibitor - Google Patents

Salt form of a human hi stone methyltransf erase ezh2 inhibitor

Info

Publication number
SG11201406468YA
SG11201406468YA SG11201406468YA SG11201406468YA SG11201406468YA SG 11201406468Y A SG11201406468Y A SG 11201406468YA SG 11201406468Y A SG11201406468Y A SG 11201406468YA SG 11201406468Y A SG11201406468Y A SG 11201406468YA SG 11201406468Y A SG11201406468Y A SG 11201406468YA
Authority
SG
Singapore
Prior art keywords
eisai
international
andover
drive
corporate
Prior art date
Application number
SG11201406468YA
Other languages
English (en)
Inventor
Kevin Wayne Kuntz
Kuan-Chun Huang
Hyeong Wook Choi
Kristen Sanders
Steven Mathieu
Arani Chanda
Frank Fang
Original Assignee
Epizyme Inc
Eisai R&D Man Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Epizyme Inc, Eisai R&D Man Co Ltd filed Critical Epizyme Inc
Publication of SG11201406468YA publication Critical patent/SG11201406468YA/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Steroid Compounds (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Hydrogenated Pyridines (AREA)
  • Pyridine Compounds (AREA)
SG11201406468YA 2012-04-13 2013-04-11 Salt form of a human hi stone methyltransf erase ezh2 inhibitor SG11201406468YA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201261624215P 2012-04-13 2012-04-13
PCT/US2013/036193 WO2013155317A1 (en) 2012-04-13 2013-04-11 Salt form of a human hi stone methyltransf erase ezh2 inhibitor

Publications (1)

Publication Number Publication Date
SG11201406468YA true SG11201406468YA (en) 2015-01-29

Family

ID=49328166

Family Applications (3)

Application Number Title Priority Date Filing Date
SG11201406468YA SG11201406468YA (en) 2012-04-13 2013-04-11 Salt form of a human hi stone methyltransf erase ezh2 inhibitor
SG10201912109QA SG10201912109QA (en) 2012-04-13 2013-04-11 Salt form of a human hi stone methyltransf erase ezh2 inhibitor
SG10201608577RA SG10201608577RA (en) 2012-04-13 2013-04-11 Salt form of a human hi stone methyltransf erase ezh2 inhibitor

Family Applications After (2)

Application Number Title Priority Date Filing Date
SG10201912109QA SG10201912109QA (en) 2012-04-13 2013-04-11 Salt form of a human hi stone methyltransf erase ezh2 inhibitor
SG10201608577RA SG10201608577RA (en) 2012-04-13 2013-04-11 Salt form of a human hi stone methyltransf erase ezh2 inhibitor

Country Status (26)

Country Link
US (7) US9394283B2 (enrdf_load_stackoverflow)
EP (4) EP3628670B1 (enrdf_load_stackoverflow)
JP (3) JP6255382B2 (enrdf_load_stackoverflow)
KR (4) KR102744039B1 (enrdf_load_stackoverflow)
CN (2) CN108358899B (enrdf_load_stackoverflow)
AU (2) AU2013245878B2 (enrdf_load_stackoverflow)
BR (1) BR112014025508B1 (enrdf_load_stackoverflow)
CA (1) CA2870005C (enrdf_load_stackoverflow)
CY (2) CY1119383T1 (enrdf_load_stackoverflow)
DK (3) DK3184523T3 (enrdf_load_stackoverflow)
ES (3) ES2617379T3 (enrdf_load_stackoverflow)
HR (2) HRP20170295T1 (enrdf_load_stackoverflow)
HU (3) HUE045353T2 (enrdf_load_stackoverflow)
IL (4) IL296199B2 (enrdf_load_stackoverflow)
IN (1) IN2014DN09068A (enrdf_load_stackoverflow)
LT (2) LT2836491T (enrdf_load_stackoverflow)
MX (2) MX362339B (enrdf_load_stackoverflow)
NZ (1) NZ700761A (enrdf_load_stackoverflow)
PL (3) PL3184523T3 (enrdf_load_stackoverflow)
PT (3) PT3628670T (enrdf_load_stackoverflow)
RS (2) RS59392B1 (enrdf_load_stackoverflow)
RU (1) RU2658911C2 (enrdf_load_stackoverflow)
SG (3) SG11201406468YA (enrdf_load_stackoverflow)
SI (2) SI2836491T1 (enrdf_load_stackoverflow)
SM (2) SMT201900501T1 (enrdf_load_stackoverflow)
WO (1) WO2013155317A1 (enrdf_load_stackoverflow)

Families Citing this family (42)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JO3438B1 (ar) 2011-04-13 2019-10-20 Epizyme Inc مركبات بنزين مستبدلة بأريل أو أريل غير متجانس
US9051269B2 (en) 2011-11-18 2015-06-09 Constellation Pharmaceuticals, Inc. Modulators of methyl modifying enzymes, compositions and uses thereof
US9085583B2 (en) 2012-02-10 2015-07-21 Constellation—Pharmaceuticals, Inc. Modulators of methyl modifying enzymes, compositions and uses thereof
US10301290B2 (en) 2012-04-13 2019-05-28 Epizyme, Inc. Combination therapy for treating cancer
CN108358899B (zh) 2012-04-13 2021-07-27 Epizyme股份有限公司 人类组蛋白甲基转移酶ezh2抑制剂的盐形式
WO2013173441A2 (en) 2012-05-16 2013-11-21 Glaxosmithkline Llc Enhancer of zeste homolog 2 inhibitors
EP2908823B1 (en) 2012-10-15 2019-09-25 Epizyme, Inc. Methods of treating cancer
MY180311A (en) 2012-10-15 2020-11-28 Epizyme Inc Substituted benzene compounds
WO2014151142A1 (en) 2013-03-15 2014-09-25 Constellation Pharmaceuticals, Inc. Modulators of methyl modifying enzymes, compositions and uses thereof
HK1214815A1 (zh) 2013-04-30 2016-08-05 Glaxosmithkline Intellectual Property (No. 2) Limited Zeste增强子同源物2的抑制剂
US9556157B2 (en) 2013-07-10 2017-01-31 Glaxosmithkline Intellectual Property (No.2) Limited Enhancer of zeste homolog 2 inhibitors
WO2015023915A1 (en) 2013-08-15 2015-02-19 Constellation Pharmaceuticals, Inc. Indole derivatives as modulators of methyl modifying enzymes, compositions and uses thereof
ES2960953T3 (es) 2013-10-16 2024-03-07 Epizyme Inc Forma de sal de clorhidrato para la inhibición de EZH2
JP2016533364A (ja) * 2013-10-18 2016-10-27 エピザイム,インコーポレイティド 癌を処置する方法
WO2015077193A1 (en) * 2013-11-19 2015-05-28 Bristol-Myers Squibb Company Inhibitors of lysine methyl transferase
CA2931263A1 (en) 2013-12-06 2015-06-11 Epizyme, Inc. Combination therapy for treating cancer
KR20230031963A (ko) 2014-06-17 2023-03-07 에피자임, 인코포레이티드 림프종 치료를 위한 ezh2 억제제
LT3157928T (lt) 2014-06-20 2019-05-27 Constellation Pharmaceuticals, Inc. 2-((4s)-6-(4-chlorfenil)-1-metil-4h-benzo[c]iizoksazolo[4,5-e]azepin-4-il)acetamido kristalinės formos
MX383635B (es) 2014-10-16 2025-03-14 Epizyme Inc Método para tratar el cáncer.
US10786511B2 (en) * 2014-11-17 2020-09-29 Epizyme, Inc. Method for treating cancer
AR102767A1 (es) 2014-12-05 2017-03-22 Lilly Co Eli Inhibidores de ezh2
AU2016252546A1 (en) 2015-04-20 2017-11-02 Epizyme, Inc. Combination therapy for treating cancer
MX387885B (es) 2015-06-10 2025-03-19 Epizyme Inc Inhibidores de ezh2 para tratar linfomas.
EA201890567A1 (ru) 2015-08-24 2018-08-31 Эпизайм, Инк. Способ лечения рака
TW201718598A (zh) 2015-08-27 2017-06-01 美國禮來大藥廠 Ezh2抑制劑
US10577350B2 (en) 2015-08-28 2020-03-03 Constellation Pharmaceuticals, Inc. Crystalline forms of (R)-N-((4-methoxy-6-methyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-2-methyl-1-(1-(1-(2,2,2-trifluoroethyl)piperidin-4-yl)ethyl)-1H-indole-3-carboxamide
US11951108B2 (en) 2016-01-29 2024-04-09 Epizyme, Inc. Combination therapy for treating cancer
EP3464643A4 (en) * 2016-06-01 2020-04-01 Epizyme Inc USE OF EZH2 INHIBITORS FOR THE TREATMENT OF CANCER
MA45406A (fr) 2016-06-17 2019-04-24 Epizyme Inc Inhibiteurs d'ezh2 pour traiter le cancer
US10457640B2 (en) 2016-10-19 2019-10-29 Constellation Pharmaceuticals, Inc. Synthesis of inhibitors of EZH2
CN110191879A (zh) * 2017-01-25 2019-08-30 恩瑞生物医药科技(上海)有限公司 一种组蛋白甲基转移酶ezh2抑制剂、其制备方法及其医药用途
WO2018183885A1 (en) 2017-03-31 2018-10-04 Epizyme, Inc. Combination therapy for treating cancer
CN110944628A (zh) 2017-06-02 2020-03-31 Epizyme股份有限公司 使用ezh2抑制剂治疗癌症
CN111093660A (zh) 2017-09-05 2020-05-01 Epizyme股份有限公司 用于治疗癌症的组合疗法
EP3823671B1 (en) 2018-07-09 2024-02-07 Fondation Asile Des Aveugles Inhibition of prc2 subunits to treat eye disorders
WO2021035194A1 (en) 2019-08-22 2021-02-25 Juno Therapeutics, Inc. Combination therapy of a t cell therapy and an enhancer of zeste homolog 2 (ezh2) inhibitor and related methods
EP4077314A1 (en) * 2019-12-20 2022-10-26 Epizyme, Inc. Crystalline hydrobromide salt of a ezh2 inhibitor, its preparation and pharmaceutical composition useful for the treatment of cancer
WO2022208552A1 (en) * 2021-03-31 2022-10-06 Msn Laboratories Private Limited, R&D Center Crystalline forms of [1,1'-Biphenyl]-3-carboxamide, N-[(1,2-dihydro-4,6-dimethyl-2-oxo-3-pyridinyl)methyl]-5-[ethyl(tetrahydro-2H-pyran-4-yl)amino]-4-methyl-4'-(4-morpholinylmethyl)-, hydrobromide (1:1) and process for its preparation thereof
WO2024229406A1 (en) 2023-05-04 2024-11-07 Revolution Medicines, Inc. Combination therapy for a ras related disease or disorder
WO2025034702A1 (en) 2023-08-07 2025-02-13 Revolution Medicines, Inc. Rmc-6291 for use in the treatment of ras protein-related disease or disorder
WO2025080946A2 (en) 2023-10-12 2025-04-17 Revolution Medicines, Inc. Ras inhibitors
WO2025171296A1 (en) 2024-02-09 2025-08-14 Revolution Medicines, Inc. Ras inhibitors

Family Cites Families (59)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0733729A (ja) 1993-07-26 1995-02-03 Kirin Brewery Co Ltd N−シアノ−n′−置換−アリールカルボキシイミダミド化合物の製造法
NZ277556A (en) 1993-12-27 1997-06-24 Eisai Co Ltd N-phenyl(alkyl)- and n-pyridyl(alkyl)anthranilic acid derivatives; intermediates
DE19516776A1 (de) 1995-05-10 1996-11-14 Boehringer Ingelheim Int Chromatin-Regulatorgene
US5741819A (en) 1995-06-07 1998-04-21 3-Dimensional Pharmaceuticals, Inc. Arylsulfonylaminobenzene derivatives and the use thereof as factor Xa inhibitors
JP3906935B2 (ja) 1995-12-18 2007-04-18 杏林製薬株式会社 N−置換ジオキソチアゾリジルベンズアミド誘導体及びその製造法
WO2000018725A1 (en) 1998-09-30 2000-04-06 The Procter & Gamble Company 2-substituted ketoamides
UA71587C2 (uk) 1998-11-10 2004-12-15 Шерінг Акцієнгезелльшафт Аміди антранілової кислоти та їхнє застосування як лікарських засобів
US6710058B2 (en) 2000-11-06 2004-03-23 Bristol-Myers Squibb Pharma Company Monocyclic or bicyclic carbocycles and heterocycles as factor Xa inhibitors
CA2433158C (en) 2000-12-28 2011-05-10 Shionogi & Co., Ltd. Pyridone derivatives having a binding activity to the cannabinoid type 2 receptor
US7700293B2 (en) 2001-08-02 2010-04-20 The Regents Of The University Of Michigan Expression profile of prostate cancer
TW200303304A (en) * 2002-02-18 2003-09-01 Astrazeneca Ab Chemical compounds
ES2333214T3 (es) 2002-02-19 2010-02-18 SHIONOGI & CO., LTD. Antipruriticos.
TW200306155A (en) 2002-03-19 2003-11-16 Du Pont Benzamides and advantageous compositions thereof for use as fungicides
US7442685B2 (en) 2003-06-13 2008-10-28 The University Of North Carolina At Chapel Hill DOT1 histone methyltransferases as a target for identifying therapeutic agents for leukemia
CN1989131A (zh) * 2004-03-30 2007-06-27 希龙公司 取代的噻吩衍生物用作抗癌药
ATE449168T1 (de) 2004-06-01 2009-12-15 Univ North Carolina Rekonstituierter histon-methyltransferase-komplex und verfahren zur identifizierung von modulatoren dafür
JO2787B1 (en) 2005-04-27 2014-03-15 امجين إنك, Alternative amide derivatives and methods of use
WO2006130720A2 (en) 2005-06-02 2006-12-07 University Of North Carolina At Chapel Hill Purification, characterization and reconstitution of a ubiquitin e3 ligase
FR2889526B1 (fr) 2005-08-04 2012-02-17 Aventis Pharma Sa 7-aza-indazoles substitues, compositions les contenant, procede de fabrication et utilisation
AR056875A1 (es) 2005-10-19 2007-10-31 Gruenenthal Gmbh Ligandos del receptor vaniloide y su aplicacion para la fabricacion de medicamentos
BRPI0617655A2 (pt) 2005-10-21 2016-08-23 Merck & Co Inc composto ou um sal farmaceuticamente aceitável do mesmo, ou um isômero óptico do mesmo, uso de um composto, e, formulação farmacêutica
WO2007053480A2 (en) 2005-10-28 2007-05-10 The University Of North Carolina At Chapel Hill Protein demethylases comprising a jmjc domain
AU2006325746A1 (en) 2005-12-14 2007-06-21 Bristol-Myers Squibb Company Six-membered heterocycles useful as serine protease inhibitors
JP5167149B2 (ja) 2006-01-20 2013-03-21 ザ・ユニヴァーシティ・オヴ・ノース・キャロライナ・アト・チャペル・ヒル 白血病の診断および治療ターゲット
EP2018166A2 (en) 2006-05-15 2009-01-28 Irm Llc Terephthalamate compounds and compositions, and their use as hiv integrase inhibitors
WO2007136592A2 (en) 2006-05-18 2007-11-29 Amphora Discovery Corporation 2-0x0-l,2-dihydr0quin0line derivatives, compositions, and uses thereof as antiproliferative agents
US8022246B2 (en) 2006-10-10 2011-09-20 The Burnham Institute For Medical Research Neuroprotective compositions and methods
WO2008103277A2 (en) 2007-02-16 2008-08-28 Amgen Inc. Nitrogen-containing heterocyclyl ketones and their use as c-met inhibitors
EP2137158A4 (en) 2007-02-28 2012-04-18 Methylgene Inc LOW-MOLECULAR INHIBITORS OF PROTEINARGININE METHYLTRANSFERASES (PRMTS)
WO2008113006A1 (en) 2007-03-14 2008-09-18 Xenon Pharmaceuticals Inc. Methods of using quinolinone compounds in treating sodium channel-mediated diseases or conditions
DE102007017884A1 (de) 2007-04-13 2008-10-16 Grünethal GmbH Neue Vanilloid-Rezeptor Liganden und ihre Verwendung zur Herstellung von Arzneimitteln
US20090012031A1 (en) 2007-07-03 2009-01-08 The Regents Of The University Of Michigan EZH2 Cancer Markers
DE102007047737A1 (de) * 2007-10-05 2009-04-30 Merck Patent Gmbh Piperidin- und Piperazinderivate
US8247401B2 (en) 2007-10-31 2012-08-21 Merck Sharp & Dohme Corp. P2X3 receptor antagonists for treatment of pain
CN101945869B (zh) 2007-12-19 2014-06-18 癌症研究技术有限公司 吡啶并[2,3-b]吡嗪-8-取代化合物及其用途
WO2009124137A2 (en) 2008-04-01 2009-10-08 Mount Sinai School Of Medicine Of New York University Method of suppressing gene transcription through histone lysine methylation
US20100113415A1 (en) 2008-05-29 2010-05-06 Rajapakse Hemaka A Epha4 rtk inhibitors for treatment of neurological and neurodegenerative disorders and cancer
US8299093B2 (en) 2008-08-08 2012-10-30 New York Blood Center, Inc. Small molecule inhibitors of retroviral assembly and maturation
FR2934995B1 (fr) 2008-08-14 2010-08-27 Sanofi Aventis Composes d'azetidines polysubstitues, leur preparation et leur application en therapeutique
US20120065247A1 (en) 2009-03-27 2012-03-15 Discoverybiomed, Inc. Modulating ires-mediated translation
WO2011011366A2 (en) 2009-07-20 2011-01-27 Constellation Pharmaceuticals Agents for stimulating activity of methyl modifying enzymes and methods of use thereof
WO2011082044A1 (en) 2009-12-30 2011-07-07 Avon Products, Inc. Topical lightening composition and uses thereof
SMT201700245T1 (it) * 2010-05-07 2017-07-18 Glaxosmithkline Llc Indoli
WO2012005805A1 (en) * 2010-05-07 2012-01-12 Glaxosmithkline Llc Azaindazoles
WO2011140325A1 (en) * 2010-05-07 2011-11-10 Glaxosmithkline Llc Indazoles
US9175331B2 (en) 2010-09-10 2015-11-03 Epizyme, Inc. Inhibitors of human EZH2, and methods of use thereof
AU2011298987B2 (en) 2010-09-10 2017-09-28 Epizyme, Inc. Inhibitors of human EZH2, and methods of use thereof
WO2012068589A2 (en) 2010-11-19 2012-05-24 Constellation Pharmaceuticals Modulators of methyl modifying enzymes, compositions and uses thereof
WO2012075080A1 (en) 2010-12-01 2012-06-07 Glaxosmithkline Llc Indoles
BR112013013668A2 (pt) 2010-12-03 2016-09-06 Epizyme Inc moduladores 7-deazapurina de histona metiltransferase, e métodos de uso dos mesmos
WO2012118812A2 (en) 2011-02-28 2012-09-07 Epizyme, Inc. Substituted 6,5-fused bicyclic heteroaryl compounds
TW201733984A (zh) 2011-04-13 2017-10-01 雅酶股份有限公司 經取代之苯化合物
JO3438B1 (ar) 2011-04-13 2019-10-20 Epizyme Inc مركبات بنزين مستبدلة بأريل أو أريل غير متجانس
WO2013138361A1 (en) 2012-03-12 2013-09-19 Epizyme, Inc. Inhibitors of human ezh2, and methods of use thereof
CN108358899B (zh) 2012-04-13 2021-07-27 Epizyme股份有限公司 人类组蛋白甲基转移酶ezh2抑制剂的盐形式
US10301290B2 (en) 2012-04-13 2019-05-28 Epizyme, Inc. Combination therapy for treating cancer
WO2013173441A2 (en) 2012-05-16 2013-11-21 Glaxosmithkline Llc Enhancer of zeste homolog 2 inhibitors
EP2908823B1 (en) 2012-10-15 2019-09-25 Epizyme, Inc. Methods of treating cancer
ES2960953T3 (es) 2013-10-16 2024-03-07 Epizyme Inc Forma de sal de clorhidrato para la inhibición de EZH2

Also Published As

Publication number Publication date
US20150065503A1 (en) 2015-03-05
DK2836491T3 (en) 2017-03-06
HUE031976T2 (en) 2017-08-28
KR102120883B1 (ko) 2020-06-09
MX2014012380A (es) 2015-07-23
US20230140327A1 (en) 2023-05-04
IL296199B2 (en) 2024-12-01
EP3628670B1 (en) 2022-10-12
CY1119383T1 (el) 2018-02-14
EP2836491B1 (en) 2016-12-07
US20190269692A1 (en) 2019-09-05
AU2018200168A1 (en) 2018-02-01
PL2836491T3 (pl) 2017-08-31
IL235045A0 (en) 2014-12-31
CN108358899A (zh) 2018-08-03
JP6255382B2 (ja) 2017-12-27
EP3628670A1 (en) 2020-04-01
PT3628670T (pt) 2022-12-02
KR20150002730A (ko) 2015-01-07
NZ700761A (en) 2016-09-30
JP2015512942A (ja) 2015-04-30
SI3184523T1 (sl) 2020-04-30
AU2018200168B2 (en) 2019-08-29
BR112014025508B1 (pt) 2020-11-17
CA2870005A1 (en) 2013-10-17
US20180243316A1 (en) 2018-08-30
WO2013155317A1 (en) 2013-10-17
IL296199B1 (en) 2024-08-01
EP2836491A4 (en) 2015-09-16
RS59392B1 (sr) 2019-11-29
CY1122883T1 (el) 2022-03-24
ES2617379T3 (es) 2017-06-16
RS55690B1 (sr) 2017-07-31
DK3628670T3 (da) 2022-12-05
CN104603130A (zh) 2015-05-06
CN108358899B (zh) 2021-07-27
PL3628670T3 (pl) 2023-02-20
LT3184523T (lt) 2020-02-10
MX362339B (es) 2019-01-11
KR20200066380A (ko) 2020-06-09
EP3184523B1 (en) 2019-06-19
CN104603130B (zh) 2018-04-27
ES2745016T3 (es) 2020-02-27
AU2013245878B2 (en) 2017-10-12
SG10201608577RA (en) 2016-12-29
PT2836491T (pt) 2017-02-08
EP2836491A1 (en) 2015-02-18
IL266165A (en) 2019-06-30
CA2870005C (en) 2021-06-22
KR20220123339A (ko) 2022-09-06
SI2836491T1 (sl) 2017-06-30
JP2018002742A (ja) 2018-01-11
KR20250005505A (ko) 2025-01-09
AU2013245878A1 (en) 2014-10-30
IL282732B2 (en) 2023-04-01
IN2014DN09068A (enrdf_load_stackoverflow) 2015-05-22
HRP20191653T1 (hr) 2020-02-21
US20250268905A1 (en) 2025-08-28
KR102744039B1 (ko) 2024-12-17
LT2836491T (lt) 2017-03-27
DK3184523T3 (da) 2019-08-19
IL296199A (en) 2022-11-01
EP3184523A1 (en) 2017-06-28
PL3184523T3 (pl) 2019-12-31
KR102438340B1 (ko) 2022-08-30
RU2658911C2 (ru) 2018-06-26
JP6634058B2 (ja) 2020-01-22
IL235045B (en) 2019-05-30
HUE045353T2 (hu) 2019-12-30
HRP20170295T1 (hr) 2017-04-21
SMT201900501T1 (it) 2019-11-13
US12251386B2 (en) 2025-03-18
MX384641B (es) 2025-03-14
US10821113B2 (en) 2020-11-03
SMT201700132T1 (it) 2017-05-08
US11491163B2 (en) 2022-11-08
IL282732A (en) 2021-06-30
IL266165B (en) 2021-06-30
EP4190777A1 (en) 2023-06-07
PT3184523T (pt) 2019-09-26
US20170143729A1 (en) 2017-05-25
US9394283B2 (en) 2016-07-19
US9872862B2 (en) 2018-01-23
RU2014145544A (ru) 2016-06-10
US10245269B2 (en) 2019-04-02
US20210137936A1 (en) 2021-05-13
HUE060881T2 (hu) 2023-04-28
IL282732B (en) 2022-12-01
JP2018199740A (ja) 2018-12-20
SG10201912109QA (en) 2020-02-27
ES2931316T3 (es) 2022-12-28

Similar Documents

Publication Publication Date Title
SG11201406468YA (en) Salt form of a human hi stone methyltransf erase ezh2 inhibitor
SG11201900135YA (en) N-(phenylsulfonyl)benzamides and related compounds as bcl-2 inhibitors
SG11201403216UA (en) Methods and compounds useful in the synthesis of orexin-2 receptor antagonists
SG11201908532UA (en) Macrocyclic compounds as ros1 kinase inhibitors
SG11201907356SA (en) Piperidine-substituted mnk inhibitors and methods related thereto
SG11201804934PA (en) Novel Compounds
SG11201909278SA (en) Fungicidal oxadiazoles
SG11201909376TA (en) Crystalline forms of a jak inhibitor compound
SG11201901197PA (en) Amino-pyrrolopyrimidinone compounds and methods of use thereof
SG11201907840RA (en) Fused imidazo-piperidine jak inhibitors
SG11201809714TA (en) Piperidines as menin inhibitors
SG11201807301SA (en) Spiro-condensed pyrrolidine derivatives as deubiquitylating enzymes (dub) inhibitors
SG11201407486PA (en) Compositions and methods for modulating utrn expression
SG11201804152RA (en) Heterocyclic compounds as immunomodulators
SG11201408641UA (en) Phenoxyethyl piperidine compounds
SG11201804647TA (en) Dosing regimens for 2-hydroxy-6-((2-(1-isopropyl-1h-pyrazol-5-yl)pyridin-3-yl)methoxy)benzaldehyde
SG11201407580YA (en) Composition comprising two antibodies engineered to have reduced and increased effector function
SG11201810268YA (en) Combination therapy with notch and pd-1 or pd-l1 inhibitors
SG11201804133PA (en) Modulators of chemokine receptors
SG11201805709RA (en) Anti-pro/latent myostatin antibodies and methods of use thereof
SG11201408271VA (en) Substituted pyrrolidines as factor xia inhibitors for the treatment thromboembolic diseases
SG11201407474VA (en) An audio signal output device and method of processing an audio signal
SG11201901203PA (en) Treatment and sustained virologic remission of hiv infection by antibodies to cd4 in haart stabilized patients
SG11201909189QA (en) 6-pyrimidin-isoindole derivative as erk1/2 inhibitor
SG11201407200TA (en) Liquid formulation