SG10201811128RA - Ezh2 inhibitors for treating lymphoma - Google Patents

Ezh2 inhibitors for treating lymphoma

Info

Publication number
SG10201811128RA
SG10201811128RA SG10201811128RA SG10201811128RA SG10201811128RA SG 10201811128R A SG10201811128R A SG 10201811128RA SG 10201811128R A SG10201811128R A SG 10201811128RA SG 10201811128R A SG10201811128R A SG 10201811128RA SG 10201811128R A SG10201811128R A SG 10201811128RA
Authority
SG
Singapore
Prior art keywords
ezh2 inhibitors
treating
ezh2
lymphoma
treating lymphoma
Prior art date
Application number
SG10201811128RA
Inventor
Heike Keilhack
Lone Ottesen
Larisa Reyderman
Sarah K Knutson
L Danielle Johnston
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 SG10201811128RA publication Critical patent/SG10201811128RA/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
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4412Non condensed pyridines; Hydrogenated derivatives thereof having oxo groups directly attached to the heterocyclic ring
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4545Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/62Oxygen or sulfur atoms
    • C07D213/63One oxygen atom
    • C07D213/65One oxygen atom attached in position 3 or 5
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

EZH2 INHIBITORS FOR TREATING LYMPHOMA The present invention relates to methods of treating cancer by administering an EZH2 inhibitor or a pharmaceutical composition thereof to the subject in need thereof. The present claims define methods for treating specific subtypes of non-Hodgkin's lymphoma comprising the administration to a subject of EZH2 inhibitors. Preferred EZH2 inhibitors include tazemetostat (EPZ-6438 E7438) and other compounds. Dosage amounts and regimes are also defined. [Figure 7]
SG10201811128RA 2014-06-17 2015-06-17 Ezh2 inhibitors for treating lymphoma SG10201811128RA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201462013522P 2014-06-17 2014-06-17
US201462036265P 2014-08-12 2014-08-12

Publications (1)

Publication Number Publication Date
SG10201811128RA true SG10201811128RA (en) 2019-01-30

Family

ID=54936086

Family Applications (2)

Application Number Title Priority Date Filing Date
SG11201610273VA SG11201610273VA (en) 2014-06-17 2015-06-17 Ezh2 inhibitors for treating lymphoma
SG10201811128RA SG10201811128RA (en) 2014-06-17 2015-06-17 Ezh2 inhibitors for treating lymphoma

Family Applications Before (1)

Application Number Title Priority Date Filing Date
SG11201610273VA SG11201610273VA (en) 2014-06-17 2015-06-17 Ezh2 inhibitors for treating lymphoma

Country Status (21)

Country Link
US (5) US10166238B2 (en)
EP (2) EP3157527B1 (en)
JP (1) JP6779793B2 (en)
KR (2) KR102497728B1 (en)
CN (2) CN113289022A (en)
AU (3) AU2015277139A1 (en)
BR (1) BR112016029492A2 (en)
CA (1) CA2952074C (en)
DK (1) DK3157527T3 (en)
EA (1) EA038337B1 (en)
ES (1) ES2948442T3 (en)
FI (1) FI3157527T3 (en)
HU (1) HUE062158T2 (en)
IL (3) IL309539A (en)
LT (1) LT3157527T (en)
MX (2) MX2021007651A (en)
PL (1) PL3157527T3 (en)
PT (1) PT3157527T (en)
SG (2) SG11201610273VA (en)
SI (1) SI3157527T1 (en)
WO (1) WO2015195848A1 (en)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2841142C (en) 2010-06-23 2020-12-15 Ryan D. Morin Biomarkers for non-hodgkin lymphomas and uses thereof
EA201691079A1 (en) 2013-12-06 2017-03-31 Эпизим, Инк. COMBINED THERAPY FOR THE TREATMENT OF ONCOLOGICAL DISEASE
CN113289022A (en) * 2014-06-17 2021-08-24 Epizyme股份有限公司 EZH2 inhibitors for the treatment of lymphoma
CN106794177A (en) 2014-10-16 2017-05-31 Epizyme股份有限公司 The method for the treatment of cancer
KR102338802B1 (en) * 2014-11-17 2021-12-14 에피자임, 인코포레이티드 Method for treating cancer
AR102767A1 (en) 2014-12-05 2017-03-22 Lilly Co Eli EZH2 INHIBITORS
MX2017013142A (en) 2015-04-20 2019-03-28 Epizyme Inc Combination therapy for treating cancer.
EP3307713A4 (en) 2015-06-10 2019-01-23 Epizyme, Inc. Ezh2 inhibitors for treating lymphoma
SG10201909199PA (en) 2015-08-24 2019-11-28 Epizyme Inc Method for treating cancer
TW201718598A (en) 2015-08-27 2017-06-01 美國禮來大藥廠 Inhibitors of EZH2
EP3407978A4 (en) 2016-01-29 2020-01-15 Epizyme Inc Combination therapy for treating cancer
EP3464643A4 (en) 2016-06-01 2020-04-01 Epizyme Inc Use of ezh2 inhibitors for treating cancer
JP2019521988A (en) * 2016-06-17 2019-08-08 エピザイム,インコーポレイティド EZH2 inhibitor for treating cancer
JP2020506905A (en) * 2017-01-20 2020-03-05 コンステレーション・ファーマシューティカルズ・インコーポレイテッドConstellation Pharmaceuticals,Inc. (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 solid dispersion
US11642346B2 (en) 2017-03-31 2023-05-09 Epizyme, Inc. Combination therapy for treating cancer
EP3630080A4 (en) 2017-06-02 2021-03-10 Epizyme, Inc. Use of ezh2 inhibitors for treating cancer
WO2019014191A1 (en) * 2017-07-10 2019-01-17 Constellation Pharmaceuticals, Inc. Ezh2 inhibitor-induced gene expression
CN111093660A (en) 2017-09-05 2020-05-01 Epizyme股份有限公司 Combination therapy for the treatment of cancer
CN110960525A (en) * 2019-11-26 2020-04-07 济南大学 Identification and evaluation of novel EED-EZH2 interaction inhibitors
CN110950834A (en) * 2019-11-26 2020-04-03 济南大学 Identification and evaluation of novel EED-EZH2 interaction small molecule inhibitors

Family Cites Families (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4522811A (en) 1982-07-08 1985-06-11 Syntex (U.S.A.) Inc. Serial injection of muramyldipeptides and liposomes enhances the anti-infective activity of muramyldipeptides
US7229774B2 (en) 2001-08-02 2007-06-12 Regents Of The University Of Michigan Expression profile of prostate cancer
US8895245B2 (en) * 2010-09-10 2014-11-25 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
AU2012223448B2 (en) 2011-02-28 2017-03-16 Epizyme, Inc. Substituted 6,5-fused bicyclic heteroaryl compounds
TW201733984A (en) 2011-04-13 2017-10-01 雅酶股份有限公司 Substituted benzene compounds
JO3438B1 (en) 2011-04-13 2019-10-20 Epizyme Inc Aryl- or heteroaryl-substituted benzene compounds
BR112014007603A2 (en) 2011-09-30 2017-06-13 Glaxosmithkline Llc cancer treatment methods
ES2718900T3 (en) * 2012-03-12 2019-07-05 Epizyme Inc Human EZH2 inhibitors and methods of use thereof
EP2836491B1 (en) 2012-04-13 2016-12-07 Epizyme, Inc. Salt form of a human histone methyltransferase ezh2 inhibitor
AU2013245661B2 (en) 2012-04-13 2017-11-23 Epizyme, Inc. Combination therapy for treating cancer
US9562041B2 (en) 2012-05-16 2017-02-07 Glaxosmithkline Llc Enhancer of zeste homolog 2 inhibitors
WO2014062732A1 (en) 2012-10-15 2014-04-24 Epizyme, Inc. Substituted benzene compounds
KR20190105669A (en) 2012-10-15 2019-09-17 에피자임, 인코포레이티드 Methods of treating cancer
JP6584952B2 (en) * 2012-11-01 2019-10-02 インフィニティー ファーマシューティカルズ, インコーポレイテッド Treatment of cancer using PI3 kinase isoform modulator
US20140120083A1 (en) 2012-11-01 2014-05-01 Infinity Pharmaceuticals, Inc. Treatment of cancers using pi3 kinase isoform modulators
US20150283142A1 (en) 2013-03-15 2015-10-08 Infinity Pharmaceuticals, Inc. Treatment of cancers using pi3 kinase isoform modulators
EP2934531A4 (en) 2012-12-19 2016-06-15 Glaxosmithkline Llc Combination
WO2014100665A1 (en) 2012-12-21 2014-06-26 Epizyme, Inc. 1,4-pyridone bicyclic heteroaryl compounds
US20150344427A1 (en) 2012-12-21 2015-12-03 Epizyme, Inc. 1,4-pyridone compounds
US20160031907A1 (en) 2013-03-15 2016-02-04 Epizyme, Inc. Substituted Benzene Compounds
EP2970306A4 (en) 2013-03-15 2016-08-03 Epizyme Inc Substituted 6,5-fused bicyclic heteroaryl compounds
DK3003309T3 (en) 2013-05-30 2020-12-14 Infinity Pharmaceuticals Inc Treatment of cancer with PI3 kinase isoform modulators
WO2015010078A2 (en) 2013-07-19 2015-01-22 Epizyme, Inc. Substituted 6,5-fused bicyclic heteroaryl compounds
WO2015010049A1 (en) 2013-07-19 2015-01-22 Epizyme, Inc. Substituted benzene compounds
ES2705573T3 (en) 2013-10-09 2019-03-26 Hoffmann La Roche Methods and compositions for detecting mutations in the human EZH2 gene
PT3057962T (en) 2013-10-16 2023-11-07 Epizyme Inc Hydrochloride salt form for ezh2 inhibition
AU2014337121A1 (en) 2013-10-18 2016-04-14 Epizyme, Inc. Method of treating cancer
EA201691079A1 (en) 2013-12-06 2017-03-31 Эпизим, Инк. COMBINED THERAPY FOR THE TREATMENT OF ONCOLOGICAL DISEASE
CN113289022A (en) 2014-06-17 2021-08-24 Epizyme股份有限公司 EZH2 inhibitors for the treatment of lymphoma
CN107249593A (en) 2014-11-06 2017-10-13 达纳-法伯癌症研究所股份有限公司 Adjusting the composition of chromatin Structure is used for the purposes of graft versus host disease (GVHD)
KR102338802B1 (en) 2014-11-17 2021-12-14 에피자임, 인코포레이티드 Method for treating cancer
JP6544507B2 (en) 2015-02-09 2019-07-17 日本精機株式会社 Head-up display device
EP3307713A4 (en) 2015-06-10 2019-01-23 Epizyme, Inc. Ezh2 inhibitors for treating lymphoma
KR20170095656A (en) 2016-02-15 2017-08-23 동부대우전자 주식회사 Washing machine having protection against heat structure

Also Published As

Publication number Publication date
SG11201610273VA (en) 2017-01-27
EP3157527A1 (en) 2017-04-26
CN106999498B (en) 2021-06-08
WO2015195848A1 (en) 2015-12-23
AU2022263523A1 (en) 2022-12-08
AU2015277139A1 (en) 2016-12-22
IL285201B2 (en) 2024-05-01
AU2020244382A1 (en) 2020-10-29
CA2952074C (en) 2022-08-30
US10166238B2 (en) 2019-01-01
MX2016016744A (en) 2017-11-30
EA038337B1 (en) 2021-08-11
EP3157527A4 (en) 2018-05-23
SI3157527T1 (en) 2023-09-29
KR102497728B1 (en) 2023-02-09
EA201692285A8 (en) 2018-01-31
US20170216300A1 (en) 2017-08-03
CN106999498A (en) 2017-08-01
US20200323866A1 (en) 2020-10-15
US11642347B2 (en) 2023-05-09
US20200022987A1 (en) 2020-01-23
JP2017518334A (en) 2017-07-06
EP3157527B1 (en) 2023-05-24
FI3157527T3 (en) 2023-07-25
HUE062158T2 (en) 2023-10-28
BR112016029492A2 (en) 2017-10-17
NZ727108A (en) 2023-09-29
IL309539A (en) 2024-02-01
CN113289022A (en) 2021-08-24
IL285201B1 (en) 2024-01-01
CA2952074A1 (en) 2015-12-23
WO2015195848A8 (en) 2016-07-07
IL249438A0 (en) 2017-02-28
EA201692285A1 (en) 2017-06-30
MX2021007651A (en) 2021-08-11
JP6779793B2 (en) 2020-11-04
PL3157527T3 (en) 2023-08-07
IL285201A (en) 2021-08-31
ES2948442T3 (en) 2023-09-12
EP4252851A2 (en) 2023-10-04
US20190175604A1 (en) 2019-06-13
PT3157527T (en) 2023-06-30
KR20230031963A (en) 2023-03-07
AU2020244382B2 (en) 2022-08-04
LT3157527T (en) 2023-07-25
US20240058348A1 (en) 2024-02-22
EP4252851A3 (en) 2023-11-22
DK3157527T3 (en) 2023-07-03
KR20170052558A (en) 2017-05-12

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