[go: up one dir, main page]

SG10201608577RA - 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
SG10201608577RA
SG10201608577RA SG10201608577RA SG10201608577RA SG10201608577RA SG 10201608577R A SG10201608577R A SG 10201608577RA SG 10201608577R A SG10201608577R A SG 10201608577RA SG 10201608577R A SG10201608577R A SG 10201608577RA SG 10201608577R A SG10201608577R A SG 10201608577RA
Authority
SG
Singapore
Prior art keywords
stone
human
salt form
ezh2 inhibitor
methyltransf erase
Prior art date
Application number
SG10201608577RA
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 SG10201608577RA publication Critical patent/SG10201608577RA/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
    • 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
    • C07D405/02Heterocyclic 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
    • 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)
  • Pyridine Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
SG10201608577RA 2012-04-13 2013-04-11 Salt form of a human hi stone methyltransf erase ezh2 inhibitor SG10201608577RA (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201261624215P 2012-04-13 2012-04-13

Publications (1)

Publication Number Publication Date
SG10201608577RA true SG10201608577RA (en) 2016-12-29

Family

ID=49328166

Family Applications (3)

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

Country Status (26)

Country Link
US (6) US9394283B2 (en)
EP (4) EP3184523B1 (en)
JP (3) JP6255382B2 (en)
KR (4) KR20250005505A (en)
CN (2) CN108358899B (en)
AU (2) AU2013245878B2 (en)
BR (1) BR112014025508B1 (en)
CA (1) CA2870005C (en)
CY (2) CY1119383T1 (en)
DK (3) DK2836491T3 (en)
ES (3) ES2745016T3 (en)
HR (2) HRP20170295T1 (en)
HU (3) HUE031976T2 (en)
IL (4) IL282732B2 (en)
IN (1) IN2014DN09068A (en)
LT (2) LT2836491T (en)
MX (2) MX384641B (en)
NZ (1) NZ700761A (en)
PL (3) PL2836491T3 (en)
PT (3) PT2836491T (en)
RS (2) RS55690B1 (en)
RU (1) RU2658911C2 (en)
SG (3) SG10201608577RA (en)
SI (2) SI2836491T1 (en)
SM (2) SMT201900501T1 (en)
WO (1) WO2013155317A1 (en)

Families Citing this family (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JO3438B1 (en) 2011-04-13 2019-10-20 Epizyme Inc Heteroaryl or aryl substituted gasoline compounds
WO2013075084A1 (en) 2011-11-18 2013-05-23 Constellation Pharmaceuticals Modulators of methyl modifying enzymes, compositions and uses thereof
NZ628762A (en) 2012-02-10 2016-07-29 Constellation Pharmaceuticals Inc Modulators of methyl modifying enzymes, compositions and uses thereof
JP6340361B2 (en) 2012-04-13 2018-06-06 エピザイム,インコーポレイティド Combination therapy to treat cancer
DK2836491T3 (en) * 2012-04-13 2017-03-06 Epizyme Inc SALT FORM OF A HUMAN HISTONMETHYL TRANSFERASE EZH2 INHIBITOR
WO2013173441A2 (en) 2012-05-16 2013-11-21 Glaxosmithkline Llc Enhancer of zeste homolog 2 inhibitors
KR102021642B1 (en) * 2012-10-15 2019-09-16 에피자임, 인코포레이티드 Methods of treating cancer
CN105102432B (en) * 2012-10-15 2019-01-04 Epizyme股份有限公司 The benzene compound being substituted
WO2014151142A1 (en) 2013-03-15 2014-09-25 Constellation Pharmaceuticals, Inc. Modulators of methyl modifying enzymes, compositions and uses thereof
SG11201508203TA (en) 2013-04-30 2015-11-27 Glaxosmithkline Ip No 2 Ltd Enhancer of zeste homolog 2 inhibitors
JP2016523955A (en) 2013-07-10 2016-08-12 グラクソスミスクライン、インテレクチュアル、プロパティー、ナンバー2、リミテッドGlaxosmithkline Intellectual Property No.2 Limited ZESTE homolog 2 enhancer inhibitor
WO2015023915A1 (en) 2013-08-15 2015-02-19 Constellation Pharmaceuticals, Inc. Indole derivatives as modulators of methyl modifying enzymes, compositions and uses thereof
CN105829302B (en) 2013-10-16 2020-09-08 Epizyme股份有限公司 Hydrochloride salt form for EZH2 inhibition
AU2014337121A1 (en) * 2013-10-18 2016-04-14 Epizyme, Inc. Method of treating cancer
US9738630B2 (en) 2013-11-19 2017-08-22 Bristol-Myers Squibb Company Inhibitors of lysine methyl transferase
EP3888659A1 (en) 2013-12-06 2021-10-06 Epizyme Inc Combination therapy for treating cancer
IL285201B2 (en) 2014-06-17 2024-05-01 Epizyme Inc Ezh2 inhibitors for treating lymphoma
CA2952830C (en) 2014-06-20 2022-11-01 Constellation Pharmaceuticals, Inc. Crystalline forms of 2-((4s)-6-(4-chlorophenyl)-1-methyl-4h-benzo[c]isoxazolo[4,5-e]azepin-4-yl)acetamide
JP2017532338A (en) 2014-10-16 2017-11-02 エピザイム,インコーポレイティド How to treat cancer
EP3220916B1 (en) * 2014-11-17 2023-04-19 Epizyme, Inc. Method for treating cancer with n-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-5-(ethyl(tetrahydro-2h-pyran-4-yl) amino)-4-methyl-4'-(morpholinomethyl)-[1,1'-biphenyl]-3-carboxamide
AR102767A1 (en) 2014-12-05 2017-03-22 Lilly Co Eli EZH2 INHIBITORS
SG11201708286PA (en) 2015-04-20 2017-11-29 Epizyme Inc Combination therapy for treating cancer
MX387885B (en) 2015-06-10 2025-03-19 Epizyme Inc Ezh2 inhibitors for treating lymphoma
CA2996412A1 (en) 2015-08-24 2017-03-02 Epizyme, Inc. Method for treating cancer
TW201718598A (en) 2015-08-27 2017-06-01 美國禮來大藥廠 Inhibitors of EZH2
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
WO2017132518A1 (en) 2016-01-29 2017-08-03 Epizyme, Inc. Combination therapy for treating cancer
US11786533B2 (en) 2016-06-01 2023-10-17 Epizyme, Inc. Use of EZH2 inhibitors for treating cancer
MA45406A (en) 2016-06-17 2019-04-24 Epizyme Inc EZH2 INHIBITORS TO TREAT CANCER
EP3529242A1 (en) 2016-10-19 2019-08-28 Constellation Pharmaceuticals, Inc. Synthesis of inhibitors of ezh2
US11214561B2 (en) * 2017-01-25 2022-01-04 Ancureall Pharmaceutical (Shanghai) Co., Ltd. Histone methyltransferase EZH2 inhibitor, preparation method and pharmaceutical use thereof
WO2018183885A1 (en) 2017-03-31 2018-10-04 Epizyme, Inc. Combination therapy for treating cancer
AU2018275123A1 (en) 2017-06-02 2020-01-30 Epizyme, Inc. Use of EZH2 inhibitors for treating cancer
EP3678663A4 (en) 2017-09-05 2021-06-02 Epizyme, Inc. COMBINATION THERAPY FOR TREATMENT OF CANCER
EP3823671B1 (en) 2018-07-09 2024-02-07 Fondation Asile Des Aveugles Inhibition of prc2 subunits to treat eye disorders
EP4017527A1 (en) 2019-08-22 2022-06-29 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
US20250154171A1 (en) 2023-10-12 2025-05-15 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 (en) 1993-07-26 1995-02-03 Kirin Brewery Co Ltd Production of n-cyano-n'-substituted-arylcarboxyimidamide compound
AU694465B2 (en) 1993-12-27 1998-07-23 Eisai Co. Ltd. Anthranilic acid derivative
DE19516776A1 (en) 1995-05-10 1996-11-14 Boehringer Ingelheim Int Chromatin regulatory genes
US5741819A (en) 1995-06-07 1998-04-21 3-Dimensional Pharmaceuticals, Inc. Arylsulfonylaminobenzene derivatives and the use thereof as factor Xa inhibitors
JP3906935B2 (en) 1995-12-18 2007-04-18 杏林製薬株式会社 N-substituted dioxothiazolidylbenzamide derivative and process for producing the same
AU6060099A (en) 1998-09-30 2000-04-17 Procter & Gamble Company, The 2-substituted ketoamides
UA71587C2 (en) 1998-11-10 2004-12-15 Шерінг Акцієнгезелльшафт Anthranilic acid amides and use thereof as medicaments
US6710058B2 (en) 2000-11-06 2004-03-23 Bristol-Myers Squibb Pharma Company Monocyclic or bicyclic carbocycles and heterocycles as factor Xa inhibitors
JP4137636B2 (en) 2000-12-28 2008-08-20 塩野義製薬株式会社 Pyridone derivatives having cannabinoid type 2 receptor affinity
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
DE60329981D1 (en) 2002-02-19 2009-12-24 Shionogi & Co antipruritics
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
JP2007531757A (en) 2004-03-30 2007-11-08 カイロン コーポレイション Substituted thiophene derivatives as anticancer agents
US7563589B2 (en) 2004-06-01 2009-07-21 The University Of North Carolina At Chapel Hill Reconstituted histone methyltransferase complex and methods of identifying modulators thereof
JO2787B1 (en) 2005-04-27 2014-03-15 امجين إنك, Substituted Amid derivatives & methods of use
ATE494548T1 (en) 2005-06-02 2011-01-15 Univ North Carolina PURIFICATION, CHARACTERIZATION AND RECOVERY OF A UBIQUITIN E3 LIGASE
FR2889526B1 (en) 2005-08-04 2012-02-17 Aventis Pharma Sa SUBSTITUTED 7-AZA-INDAZOLES, COMPOSITIONS CONTAINING SAME, PROCESS FOR PRODUCTION AND USE
PL1940821T3 (en) 2005-10-19 2013-08-30 Gruenenthal Gmbh Novel vanilloid receptor ligands and their use for producing medicaments
CN101291910A (en) 2005-10-21 2008-10-22 默克公司 Potassium channel inhibitors
WO2007053480A2 (en) 2005-10-28 2007-05-10 The University Of North Carolina At Chapel Hill Protein demethylases comprising a jmjc domain
CN101341124A (en) 2005-12-14 2009-01-07 布里斯托尔-迈尔斯斯奎布公司 Six-membered heterocycles useful as serine protease inhibitors
AU2006336552B2 (en) 2006-01-20 2012-12-20 The University Of North Carolina At Chapel Hill Diagnostic and therapeutic targets for leukemia
RU2008149246A (en) 2006-05-15 2010-06-20 Айрм Ллк (Bm) TERPHTHALATE BASED COMPOUND, COMPOSITIONS AND THEIR APPLICATION AS HIV INTEGRAS INHIBITORS
EP2040711A2 (en) 2006-05-18 2009-04-01 Amphora Discovery Corporation 2-oxo-1,2-dihydroquinoline derivatives, compositions, and uses thereof as antiproliferative agents
EP2086318A4 (en) 2006-10-10 2009-12-23 Burnham Inst Medical Research NEUROPROTEKTIVE COMPOSITIONS AND METHOD
US8314087B2 (en) 2007-02-16 2012-11-20 Amgen Inc. Nitrogen-containing heterocyclyl ketones and methods of use
US8338437B2 (en) 2007-02-28 2012-12-25 Methylgene Inc. Amines as small molecule inhibitors
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 (en) 2007-04-13 2008-10-16 Grünethal GmbH Novel vanilloid receptor ligands and their use in the preparation of medicines
US20090012031A1 (en) 2007-07-03 2009-01-08 The Regents Of The University Of Michigan EZH2 Cancer Markers
DE102007047737A1 (en) * 2007-10-05 2009-04-30 Merck Patent Gmbh Piperidine and piperazine derivatives
US8247401B2 (en) 2007-10-31 2012-08-21 Merck Sharp & Dohme Corp. P2X3 receptor antagonists for treatment of pain
MX2010006739A (en) 2007-12-19 2010-10-08 Cancer Rec Tech Ltd Pyrido[2,3-b]pyrazine-8-substituted compounds and their use.
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
AU2009279616A1 (en) 2008-08-08 2010-02-11 New York Blood Center Small molecule inhibitors of retroviral assembly and maturation
FR2934995B1 (en) 2008-08-14 2010-08-27 Sanofi Aventis POLYSUBSTITUTED AZETIDINE COMPOUNDS, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF
JP2012522013A (en) 2009-03-27 2012-09-20 ザ ユーエービー リサーチ ファウンデーション Regulated IRES-mediated translation
US20110021362A1 (en) 2009-07-20 2011-01-27 Constellation Pharmaceuticals Agents for stimulating activity of methyl modifying enzymes and methods of use thereof
EP2521558A4 (en) 2009-12-30 2013-07-03 Avon Prod Inc Topical lightening composition and uses thereof
LT2566327T (en) 2010-05-07 2017-05-25 Glaxosmithkline Llc Indoles
US8637509B2 (en) * 2010-05-07 2014-01-28 Glaxosmithkline Llc Azaindazoles
US8846935B2 (en) * 2010-05-07 2014-09-30 Glaxosmithkline Llc Indazoles
AU2011298987B2 (en) 2010-09-10 2017-09-28 Epizyme, Inc. Inhibitors of human EZH2, and methods of use thereof
US9175331B2 (en) 2010-09-10 2015-11-03 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
JP5908493B2 (en) 2010-12-01 2016-04-26 グラクソスミスクライン・リミテッド・ライアビリティ・カンパニーGlaxoSmithKline LLC Indole
EP2646454B1 (en) 2010-12-03 2015-07-08 Epizyme, Inc. 7-deazapurine modulators of histone methyltransferase, and methods of use thereof
EP3323820B1 (en) 2011-02-28 2023-05-10 Epizyme, Inc. Substituted 6,5-fused bicyclic heteroaryl compounds
TWI598336B (en) 2011-04-13 2017-09-11 雅酶股份有限公司 Substituted benzene compounds
JO3438B1 (en) 2011-04-13 2019-10-20 Epizyme Inc Heteroaryl or aryl substituted gasoline compounds
AU2013232229B2 (en) 2012-03-12 2017-11-23 Epizyme, Inc. Inhibitors of human EZH2, and methods of use thereof
DK2836491T3 (en) 2012-04-13 2017-03-06 Epizyme Inc SALT FORM OF A HUMAN HISTONMETHYL TRANSFERASE EZH2 INHIBITOR
JP6340361B2 (en) 2012-04-13 2018-06-06 エピザイム,インコーポレイティド Combination therapy to treat cancer
WO2013173441A2 (en) 2012-05-16 2013-11-21 Glaxosmithkline Llc Enhancer of zeste homolog 2 inhibitors
KR102021642B1 (en) 2012-10-15 2019-09-16 에피자임, 인코포레이티드 Methods of treating cancer
CN105829302B (en) 2013-10-16 2020-09-08 Epizyme股份有限公司 Hydrochloride salt form for EZH2 inhibition

Also Published As

Publication number Publication date
IL282732A (en) 2021-06-30
JP6255382B2 (en) 2017-12-27
PT2836491T (en) 2017-02-08
RU2014145544A (en) 2016-06-10
JP6634058B2 (en) 2020-01-22
AU2013245878B2 (en) 2017-10-12
SI3184523T1 (en) 2020-04-30
HUE060881T2 (en) 2023-04-28
CY1119383T1 (en) 2018-02-14
SMT201700132T1 (en) 2017-05-08
AU2018200168B2 (en) 2019-08-29
MX2014012380A (en) 2015-07-23
WO2013155317A1 (en) 2013-10-17
CN108358899B (en) 2021-07-27
AU2018200168A1 (en) 2018-02-01
EP4190777A1 (en) 2023-06-07
BR112014025508B1 (en) 2020-11-17
CA2870005A1 (en) 2013-10-17
EP3184523B1 (en) 2019-06-19
US20230140327A1 (en) 2023-05-04
MX362339B (en) 2019-01-11
IL296199B1 (en) 2024-08-01
EP3184523A1 (en) 2017-06-28
US20180243316A1 (en) 2018-08-30
US11491163B2 (en) 2022-11-08
US9872862B2 (en) 2018-01-23
US20210137936A1 (en) 2021-05-13
RU2658911C2 (en) 2018-06-26
JP2015512942A (en) 2015-04-30
LT2836491T (en) 2017-03-27
IL282732B2 (en) 2023-04-01
US20190269692A1 (en) 2019-09-05
HRP20170295T1 (en) 2017-04-21
RS59392B1 (en) 2019-11-29
HUE031976T2 (en) 2017-08-28
EP2836491B1 (en) 2016-12-07
KR20200066380A (en) 2020-06-09
EP3628670B1 (en) 2022-10-12
PL3184523T3 (en) 2019-12-31
US9394283B2 (en) 2016-07-19
MX384641B (en) 2025-03-14
SG11201406468YA (en) 2015-01-29
AU2013245878A1 (en) 2014-10-30
KR102120883B1 (en) 2020-06-09
NZ700761A (en) 2016-09-30
US20150065503A1 (en) 2015-03-05
ES2931316T3 (en) 2022-12-28
PL2836491T3 (en) 2017-08-31
IL266165B (en) 2021-06-30
HRP20191653T1 (en) 2020-02-21
EP3628670A1 (en) 2020-04-01
KR102438340B1 (en) 2022-08-30
IL296199A (en) 2022-11-01
KR20150002730A (en) 2015-01-07
DK2836491T3 (en) 2017-03-06
CA2870005C (en) 2021-06-22
SI2836491T1 (en) 2017-06-30
US10245269B2 (en) 2019-04-02
US20170143729A1 (en) 2017-05-25
ES2745016T3 (en) 2020-02-27
PT3628670T (en) 2022-12-02
JP2018199740A (en) 2018-12-20
IL296199B2 (en) 2024-12-01
ES2617379T3 (en) 2017-06-16
KR20250005505A (en) 2025-01-09
KR102744039B1 (en) 2024-12-17
CN108358899A (en) 2018-08-03
IL282732B (en) 2022-12-01
US10821113B2 (en) 2020-11-03
US12251386B2 (en) 2025-03-18
EP2836491A1 (en) 2015-02-18
DK3184523T3 (en) 2019-08-19
IN2014DN09068A (en) 2015-05-22
PT3184523T (en) 2019-09-26
PL3628670T3 (en) 2023-02-20
IL235045B (en) 2019-05-30
SMT201900501T1 (en) 2019-11-13
LT3184523T (en) 2020-02-10
CN104603130A (en) 2015-05-06
HUE045353T2 (en) 2019-12-30
IL235045A0 (en) 2014-12-31
JP2018002742A (en) 2018-01-11
SG10201912109QA (en) 2020-02-27
EP2836491A4 (en) 2015-09-16
CN104603130B (en) 2018-04-27
CY1122883T1 (en) 2022-03-24
KR20220123339A (en) 2022-09-06
RS55690B1 (en) 2017-07-31
IL266165A (en) 2019-06-30
DK3628670T3 (en) 2022-12-05

Similar Documents

Publication Publication Date Title
IL266165B (en) Salt form of a human hi stone methyltransf erase ezh2 inhibitor
IL259958B (en) Heterocyclic inhibitors of glutaminase
IL232599A (en) Hydrobromide salt of pridopidine
EP2678018A4 (en) Combination of kanase inhibitors and uses thereof
IL230901A0 (en) Pyrazol-4-yl-heterocyclyl-carboxamide compounds and methods of use
IL232292A0 (en) Use of anti-connexin agents for enhancing the therapeutic effect of acetylcholinesterase inhibitors
ZA201401417B (en) Novel soft rock inhibitors
PH12013502483A1 (en) Use of a metal salt of 2-mercaptobenzothiazole
ZA201307496B (en) Novel rock inhibitors
EP2760853A4 (en) Novel salts of alogliptin
EP2709999A4 (en) Quinazoline-7-ether compounds and methods of use
GB201114854D0 (en) Novel rock inhibitors
PT2709584T (en) Sensory use of 6-cyclopentylidenehexane derivatives
GB201117252D0 (en) Improved treatment of hard surfaces
ZA201205358B (en) Use of a salt of bistetrazolylamine
ZA201308872B (en) Use of a dinitromethane salt