SG11201807834WA - Bridged bicyclic inhibitors of menin-mll and methods of use - Google Patents

Bridged bicyclic inhibitors of menin-mll and methods of use

Info

Publication number
SG11201807834WA
SG11201807834WA SG11201807834WA SG11201807834WA SG11201807834WA SG 11201807834W A SG11201807834W A SG 11201807834WA SG 11201807834W A SG11201807834W A SG 11201807834WA SG 11201807834W A SG11201807834W A SG 11201807834WA SG 11201807834W A SG11201807834W A SG 11201807834WA
Authority
SG
Singapore
Prior art keywords
huron
floor
international
ann arbor
parkway
Prior art date
Application number
SG11201807834WA
Other languages
English (en)
Inventor
Tao Wu
Liansheng Li
Yi Wang
Pingda Ren
Jolanta Grembecka
Tomasz Cierpicki
Szymon Klossowski
Jonathan Pollock
Dmitry Borkin
Original Assignee
Kura Oncology Inc
Univ Michigan Regents
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 Kura Oncology Inc, Univ Michigan Regents filed Critical Kura Oncology Inc
Publication of SG11201807834WA publication Critical patent/SG11201807834WA/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04Ortho-condensed systems
    • 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
    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • 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
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
SG11201807834WA 2016-03-16 2017-03-15 Bridged bicyclic inhibitors of menin-mll and methods of use SG11201807834WA (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201662309362P 2016-03-16 2016-03-16
US201662431387P 2016-12-07 2016-12-07
PCT/US2017/022535 WO2017161002A1 (en) 2016-03-16 2017-03-15 Bridged bicyclic inhibitors of menin-mll and methods of use

Publications (1)

Publication Number Publication Date
SG11201807834WA true SG11201807834WA (en) 2018-10-30

Family

ID=59851929

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11201807834WA SG11201807834WA (en) 2016-03-16 2017-03-15 Bridged bicyclic inhibitors of menin-mll and methods of use

Country Status (17)

Country Link
US (2) US10752639B2 (de)
EP (1) EP3429585B1 (de)
JP (1) JP7000333B2 (de)
KR (1) KR102419524B1 (de)
CN (1) CN109640987B (de)
AU (1) AU2017235462B2 (de)
BR (1) BR112018068702A2 (de)
CA (1) CA3015845A1 (de)
HK (1) HK1258821A1 (de)
IL (1) IL261625B (de)
MA (1) MA43823A (de)
MX (1) MX2018011092A (de)
PH (1) PH12018501955A1 (de)
SG (1) SG11201807834WA (de)
TW (1) TWI743096B (de)
WO (1) WO2017161002A1 (de)
ZA (1) ZA201805845B (de)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016040330A1 (en) 2014-09-09 2016-03-17 The Regents Of The University Of Michigan Thienopyrimidine and thienopyridine compounds and methods of use thereof
EP3302057A4 (de) 2015-06-04 2018-11-21 Kura Oncology, Inc. Verfahren und zusammensetzungen zur hemmung der interaktion von menin mit mll-proteinen
TWI703150B (zh) 2015-06-04 2020-09-01 美商庫拉腫瘤技術股份有限公司 用於抑制menin及mll蛋白之交互作用的方法及組合物
IL261606B (en) 2016-03-16 2022-09-01 Kura Oncology Inc Inhibitors of converted menin-mll and methods of use
MA43823A (fr) 2016-03-16 2018-11-28 Kura Oncology Inc Inhibiteurs bicycliques pontés de ménine-mll et méthodes d'utilisation
CA3022868A1 (en) 2016-05-02 2017-11-09 Shaomeng Wang Piperidines as menin inhibitors
EP3512857B1 (de) 2016-09-14 2021-02-24 Janssen Pharmaceutica NV Spiro-bizyklische inhibitoren von menin-mll-wechselwirkung
EP3512858B1 (de) 2016-09-14 2023-11-08 Janssen Pharmaceutica NV Kondensierte bicyclische inhibitoren der menin-mll-interaktion
AU2017376599B2 (en) 2016-12-15 2021-10-07 Janssen Pharmaceutica Nv Azepane inhibitors of menin-MLL interaction
EA201991448A1 (ru) 2017-01-06 2019-12-30 Янссен Фармацевтика Нв Азепановые ингибиторы взаимодействия менин-mll
US11944627B2 (en) * 2017-03-24 2024-04-02 Kura Oncology, Inc. Methods for treating hematological malignancies and Ewing's sarcoma
MX2019011412A (es) 2017-03-31 2020-02-07 Univ Michigan Regents Piperidinas como inhibidores de menina covalentes.
US11542248B2 (en) 2017-06-08 2023-01-03 Kura Oncology, Inc. Methods and compositions for inhibiting the interaction of menin with MLL proteins
TW201920170A (zh) * 2017-09-20 2019-06-01 美商庫拉腫瘤技術股份有限公司 經取代之menin-mll 抑制劑及使用方法
US11396517B1 (en) 2017-12-20 2022-07-26 Janssen Pharmaceutica Nv Exo-aza spiro inhibitors of menin-MLL interaction
CN110204552B (zh) * 2018-02-28 2021-08-17 中国科学院上海药物研究所 一类噻吩并[3,2-d]嘧啶衍生物、其制备方法、药物组合物与用途
US11325921B2 (en) 2018-03-30 2022-05-10 Sumitomo Dainippon Pharma Co., Ltd. Optically active crosslinked cyclic secondary amine derivative
EP3856173A4 (de) * 2018-09-26 2022-07-06 Kura Oncology, Inc. Behandlung hämatologischen malignitäten mit inhibitoren von menin
CN110964016B (zh) * 2018-09-29 2021-05-28 南京药捷安康生物科技有限公司 氨基降茨烷衍生物及其制备方法与应用
SG11202104243VA (en) * 2018-12-06 2021-05-28 Daiichi Sankyo Co Ltd Cycloalkane-1,3-diamine derivative
TW202043205A (zh) 2018-12-31 2020-12-01 美商拜歐米富士恩有限公司 Menin-mll相互作用之抑制劑
CN111297863B (zh) * 2020-03-30 2021-06-25 四川大学华西医院 menin-MLL抑制剂在制备治疗子宫内膜癌的药物中的应用
US20230165858A1 (en) * 2020-04-07 2023-06-01 Syndax Pharmaceuticals, Inc. Combinations of menin inhibitors and cyp3a4 inhibitors and methods of use thereof
CN117321049A (zh) 2021-05-08 2023-12-29 詹森药业有限公司 取代的螺环衍生物
EP4334320A1 (de) 2021-05-08 2024-03-13 JANSSEN Pharmaceutica NV Substituierte spiroderivate
AR125866A1 (es) 2021-05-14 2023-08-23 Syndax Pharmaceuticals Inc Inhibidores de la interacción de menina-mll
EP4347588A1 (de) 2021-06-01 2024-04-10 JANSSEN Pharmaceutica NV Substituierte phenyl-1h-pyrrolo[2,3-c pyridin-derivate
CN117425659A (zh) 2021-06-03 2024-01-19 詹森药业有限公司 哒嗪或被螺环胺取代的1,2,4-三嗪
KR20240021808A (ko) 2021-06-17 2024-02-19 얀센 파마슈티카 엔브이 암과 같은 질환의 치료를 위한 (r)-n-에틸-5-플루오로-n-아이소프로필-2-((5-(2-(6-((2-메톡시에틸)(메틸)아미노)-2-메틸헥산-3-일)-2,6-다이아자스피로[3.4]옥탄-6-일)-1,2,4-트라이아진-6-일)옥시)벤즈아미드 베실레이트 염
WO2023220098A1 (en) * 2022-05-09 2023-11-16 Syndax Pharmaceuticals, Inc. Menin-mll inhibitors for the treatment of cancer

Family Cites Families (92)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US510A (en) 1837-12-07 soeel
US5863A (en) 1848-10-17 Matthias p
US949A (en) 1838-09-27 Improvement in roller cotton-gins for ginning long-staple and other kinds of cotton
US5861A (en) 1848-10-17 Locking umbrella and parasol
US1007727A (en) 1908-02-17 1911-11-07 Oscar F Onken Auxiliary table-top.
US5052558A (en) 1987-12-23 1991-10-01 Entravision, Inc. Packaged pharmaceutical product
US5033252A (en) 1987-12-23 1991-07-23 Entravision, Inc. Method of packaging and sterilizing a pharmaceutical product
GB8827305D0 (en) 1988-11-23 1988-12-29 British Bio Technology Compounds
US5323907A (en) 1992-06-23 1994-06-28 Multi-Comp, Inc. Child resistant package assembly for dispensing pharmaceutical medications
DE4239169A1 (de) 1992-11-21 1994-05-26 Merck Patent Gmbh Cyclobutan - Benzol - Derivate
US5455258A (en) 1993-01-06 1995-10-03 Ciba-Geigy Corporation Arylsulfonamido-substituted hydroxamic acids
US5863949A (en) 1995-03-08 1999-01-26 Pfizer Inc Arylsulfonylamino hydroxamic acid derivatives
EP0821671B1 (de) 1995-04-20 2000-12-27 Pfizer Inc. Arylsulfonamido-substituierte hydroxamsäure derivate als inhibitoren von mmp und tnf
DK0780386T3 (da) 1995-12-20 2003-02-03 Hoffmann La Roche Matrixmetalloproteaseinhibitorer
JP3195756B2 (ja) 1996-07-04 2001-08-06 公子 吉水 潤滑補助体
EP0923585B1 (de) 1996-07-18 2002-05-08 Pfizer Inc. Matrix metalloprotease-inhibitoren auf basis von phosphinsäuren
JP3333870B2 (ja) 1996-07-26 2002-10-15 国土交通省北陸地方整備局長 草刈機
JP2000501423A (ja) 1996-08-23 2000-02-08 ファイザー インク. アリールスルホニルアミノヒドロキサム酸誘導体
US5866562A (en) 1996-10-25 1999-02-02 Bayer Aktiengesellschaft Ring-bridged bis-quinolines
PT950059E (pt) 1997-01-06 2004-10-29 Pfizer Derivados de sulfona ciclicos
ID22799A (id) 1997-02-03 1999-12-09 Pfizer Prod Inc Turunan-turunan asam arilsulfonilamino hidroksamat
JP2000507975A (ja) 1997-02-07 2000-06-27 ファイザー・インク N−ヒドロキシ−β−スルホニルプロピオンアミド誘導体類及びそれらのマトリックスメタロプロテイナーゼ阻害薬としての使用
IL131123A0 (en) 1997-02-11 2001-01-28 Pfizer Arylsulfonyl hydroxamic acid derivatives
JPH10330377A (ja) 1997-06-02 1998-12-15 Kyowa Hakko Kogyo Co Ltd ピペリジン誘導体
GB9725782D0 (en) 1997-12-05 1998-02-04 Pfizer Ltd Therapeutic agents
GB9801690D0 (en) 1998-01-27 1998-03-25 Pfizer Ltd Therapeutic agents
US6479487B1 (en) 1998-02-26 2002-11-12 Aventis Pharmaceuticals Inc. 6, 9-disubstituted 2-[trans-(4-aminocyclohexyl)amino] purines
PA8469501A1 (es) 1998-04-10 2000-09-29 Pfizer Prod Inc Hidroxamidas del acido (4-arilsulfonilamino)-tetrahidropiran-4-carboxilico
PA8469401A1 (es) 1998-04-10 2000-05-24 Pfizer Prod Inc Derivados biciclicos del acido hidroxamico
PA8474101A1 (es) 1998-06-19 2000-09-29 Pfizer Prod Inc Compuestos de pirrolo [2,3-d] pirimidina
WO2002088107A1 (en) 2001-04-26 2002-11-07 Eisai Co., Ltd. Nitrogenous fused-ring compound having pyrazolyl group as substituent and medicinal composition thereof
CN100343258C (zh) 2001-04-30 2007-10-17 美国拜尔公司 新的4-氨基-5,6-取代的噻吩并[2,3-d]嘧啶化合物
WO2003022214A2 (en) 2001-09-06 2003-03-20 Millennium Pharmaceuticals, Inc. Piperazine and homopiperazine compounds
WO2004030671A2 (en) 2002-10-02 2004-04-15 Merck Patent Gmbh Use of 4-amino-quinazolines as anti cancer agents
AU2003255482A1 (en) 2002-10-02 2004-04-23 Merck Patent Gmbh Use of 4 amino-quinazolines as anti cancer agents
US20050222175A1 (en) 2004-03-31 2005-10-06 Dhanoa Dale S New piperidinylamino-thieno[2,3-D] pyrimidine compounds
NZ542236A (en) 2003-03-31 2008-05-30 Predix Pharmaceuticals Holding New piperidinylamino-thieno[2,3-d]pyrimidine compounds
US7612078B2 (en) 2003-03-31 2009-11-03 Epix Delaware, Inc. Piperidinylamino-thieno[2,3-D] pyrimidine compounds
US8362264B2 (en) 2003-08-22 2013-01-29 Dendreon Corporation Compositions and methods for the treatment of disease associated with Trp-p8 expression
US20050123906A1 (en) 2003-11-06 2005-06-09 Rana Tariq M. Protein modulation
EP1768964A1 (de) 2004-07-06 2007-04-04 Angion Biomedica Corporation Chinazolinmodulatoren des hepatozytenwachstumsfaktors/der c-met-aktivität für die behandlung von krebs
US7553964B2 (en) * 2005-06-03 2009-06-30 Abbott Laboratories Cyclobutyl amine derivatives
US20060281769A1 (en) 2005-06-10 2006-12-14 Baumann Christian A Synergistic modulation of flt3 kinase using thienopyrimidine and thienopyridine kinase modulators
US20060281771A1 (en) 2005-06-10 2006-12-14 Baumann Christian A Synergistic modulation of flt3 kinase using aminoquinoline and aminoquinazoline kinase modulators
EP1937272A2 (de) 2005-09-02 2008-07-02 Tibotec Pharmaceuticals Ltd. Benzodiazepine als hcv-hemmer
EP1926798B1 (de) 2005-09-19 2009-09-30 Merck Patent GmbH Cyclobutan- und spiro[3.3]heptanverbindungen
FR2891829A1 (fr) 2005-10-12 2007-04-13 Sanofi Aventis Sa Derives de la 4-amino-quinazoline, leur preparation et leur application en therapeutique
WO2007076034A2 (en) 2005-12-21 2007-07-05 Abbott Laboratories Anti-viral compounds
EP2004656B1 (de) 2006-04-07 2013-07-10 Boehringer Ingelheim International GmbH Thienopyrimidine mit mnk1/mnk2-hemmender wirkung für pharmazeutische zusammensetzungen
EP1903044A1 (de) 2006-09-14 2008-03-26 Novartis AG Adenosinderivate als Agonisten des A2A-Rezeptors
US8242078B2 (en) * 2006-10-19 2012-08-14 The University Of Chicago Therapeutics to inhibit MLL-menin interaction for treating leukemia
EP1947103A1 (de) 2007-01-22 2008-07-23 4Sc Ag Aryloxypropanolamine, Herstellungsverfahren dafür und Verwendung von Aryloxypropanolaminen als Arzneimittel
WO2008099019A1 (en) 2007-02-16 2008-08-21 Tibotec Pharmaceuticals Ltd. 6-hydroxy-dibenzodiazepinones useful as hepatitis c virus inhibitors
FR2913017A1 (fr) 2007-02-23 2008-08-29 Cerep Sa Derives de piperidine et piperazine comme agents anti-neoplasiques ou inhibiteurs de proliferation cellulaire
ATE496022T1 (de) 2007-03-19 2011-02-15 Council Scient Ind Res Anthranilsäure-derivat als antikrebswirkstoff und verfahren zur herstellung davon
WO2008135232A1 (en) 2007-05-02 2008-11-13 Riccardo Cortese Use and compositions of purine derivatives for the treatment of proliferative disorders
WO2008153760A1 (en) 2007-05-25 2008-12-18 Burnham Institute For Medical Research Inhibitors of thapsigargin-induced cell death
WO2009017838A2 (en) 2007-08-01 2009-02-05 Exelixis, Inc. Combinations of jak-2 inhibitors and other agents
WO2009064388A2 (en) 2007-11-09 2009-05-22 Liu Jun O Inhibitors of human methionine aminopeptidase 1 and methods of treating disorders
CA2709784A1 (en) 2007-12-21 2009-07-09 University Of Rochester Method for altering the lifespan of eukaryotic organisms
CN102105463A (zh) 2008-05-22 2011-06-22 阿勒根公司 对cxcr4受体有活性的二环化合物
DE102008027574A1 (de) 2008-06-10 2009-12-17 Merck Patent Gmbh Neue Pyrrolidinderivate als MetAP-2 Inhibitoren
KR101354763B1 (ko) 2008-08-25 2014-01-22 아이알엠 엘엘씨 헷지호그 경로 조절제
WO2010030757A2 (en) 2008-09-10 2010-03-18 Kalypsys Inc. Aminopyrimidine inhibitors of histamine receptors for the treatment of disease
JP5690823B2 (ja) 2009-07-08 2015-03-25 レオ ファーマ アクティーゼルスカブ Jak受容体およびタンパク質チロシンキナーゼ阻害薬としての複素環化合物
US8742100B2 (en) 2009-07-30 2014-06-03 National University Of Singapore Small molecule inhibitors of isoprenylcysteine carboxyl methyltransferase with potential anticancer activity
CA2773131C (en) 2009-09-04 2015-07-14 The Regents Of The University Of Michigan Compositions and methods for treatment of leukemia
WO2011101069A2 (en) 2010-02-22 2011-08-25 Merck Patent Gmbh Hetarylaminonaphthyridines
WO2012022265A1 (en) 2010-08-20 2012-02-23 Hutchison Medipharma Limited Pyrrolopyrimidine compounds and uses thereof
US9090624B2 (en) * 2011-08-04 2015-07-28 Allergan, Inc. Aromatic bycyclic derivatives as CXCR4 receptor modulators
GB201114212D0 (en) 2011-08-18 2011-10-05 Ucb Pharma Sa Therapeutic agents
AR090037A1 (es) 2011-11-15 2014-10-15 Xention Ltd Derivados de tieno y/o furo-pirimidinas y piridinas inhibidores de los canales de potasio
CN103833759A (zh) * 2012-11-23 2014-06-04 华东理工大学 作为blk、flt3抑制剂的蝶啶酮衍生物及其应用
EP2968285A4 (de) 2013-03-13 2016-12-21 Flatley Discovery Lab Verbindungen und verfahren zur behandlung von zystischer fibrose
BR112015022602A2 (pt) * 2013-03-13 2017-07-18 Univ Michigan Regents composições compreendendo compostos de tienopirimidina e tienopiridina e métodos de uso dos mesmos
US9212180B2 (en) * 2013-06-12 2015-12-15 The Regents Of The University Of Michigan Menin-MLL inhibitors and methods of use thereof
EP3489232A3 (de) * 2014-04-04 2019-07-31 Syros Pharmaceuticals, Inc. Hemmer der cyclinabhängigen kinase 7 (cdk7)
US20170119769A1 (en) * 2014-06-10 2017-05-04 The Trustees Of The University Of Pennsylvania Scaffolds for inhibitors of menin-mll interactions
WO2016040330A1 (en) 2014-09-09 2016-03-17 The Regents Of The University Of Michigan Thienopyrimidine and thienopyridine compounds and methods of use thereof
TWI703150B (zh) 2015-06-04 2020-09-01 美商庫拉腫瘤技術股份有限公司 用於抑制menin及mll蛋白之交互作用的方法及組合物
EP3302057A4 (de) 2015-06-04 2018-11-21 Kura Oncology, Inc. Verfahren und zusammensetzungen zur hemmung der interaktion von menin mit mll-proteinen
CN108779116A (zh) 2015-12-22 2018-11-09 生命医药公司 多发性内分泌瘤蛋白-mll相互作用的抑制剂
WO2017132398A1 (en) 2016-01-26 2017-08-03 Memorial Sloan-Kettering Cancer Center Targeting chromatin regulators inhibits leukemogenic gene expression in npm1 mutant leukemia
MA43823A (fr) 2016-03-16 2018-11-28 Kura Oncology Inc Inhibiteurs bicycliques pontés de ménine-mll et méthodes d'utilisation
IL261606B (en) 2016-03-16 2022-09-01 Kura Oncology Inc Inhibitors of converted menin-mll and methods of use
CA3022868A1 (en) 2016-05-02 2017-11-09 Shaomeng Wang Piperidines as menin inhibitors
WO2017207387A1 (en) 2016-05-31 2017-12-07 Bayer Pharma Aktiengesellschaft Spiro condensed azetidine derivatives as inhibitors of the menin-mml1 interaction
MX2018015252A (es) 2016-06-10 2019-04-25 Vitae Pharmaceuticals Inc Inhibidores de la interaccion de menina-leucemia de linaje mixto.
WO2018024602A1 (en) 2016-08-04 2018-02-08 Bayer Aktiengesellschaft 2,7-diazaspiro[4.4]nonanes
EP3512858B1 (de) 2016-09-14 2023-11-08 Janssen Pharmaceutica NV Kondensierte bicyclische inhibitoren der menin-mll-interaktion
CA3033239A1 (en) 2016-09-14 2018-03-22 Janssen Pharmaceutica Nv Spiro bicyclic inhibitors of menin-mll interaction
EP4230627A3 (de) 2016-09-16 2023-11-15 Vitae Pharmaceuticals, LLC Inhibitoren der menin-mll-interaktion

Also Published As

Publication number Publication date
CA3015845A1 (en) 2017-09-21
AU2017235462A1 (en) 2018-09-27
JP7000333B2 (ja) 2022-02-10
JP2019508426A (ja) 2019-03-28
KR20180127406A (ko) 2018-11-28
US20210107917A1 (en) 2021-04-15
ZA201805845B (en) 2023-03-29
MX2018011092A (es) 2018-11-22
US10752639B2 (en) 2020-08-25
MA43823A (fr) 2018-11-28
CN109640987A (zh) 2019-04-16
TW201742870A (zh) 2017-12-16
CN109640987B (zh) 2022-12-02
EP3429585A4 (de) 2019-10-09
EP3429585A1 (de) 2019-01-23
TWI743096B (zh) 2021-10-21
AU2017235462B2 (en) 2021-07-01
WO2017161002A1 (en) 2017-09-21
KR102419524B1 (ko) 2022-07-08
HK1258821A1 (zh) 2019-11-22
PH12018501955A1 (en) 2019-06-17
BR112018068702A2 (pt) 2019-01-15
US11555041B2 (en) 2023-01-17
IL261625A (en) 2018-10-31
US20190092783A1 (en) 2019-03-28
IL261625B (en) 2021-08-31
EP3429585B1 (de) 2021-11-24

Similar Documents

Publication Publication Date Title
SG11201807834WA (en) Bridged bicyclic inhibitors of menin-mll and methods of use
SG11201807982UA (en) Substituted inhibitors of menin-mll and methods of use
SG11201909955XA (en) Formulations of anti-lag3 antibodies and co-formulations of anti-lag3 antibodies and anti-pd-1 antibodies
SG11201900677SA (en) Combination therapies of chimeric antigen receptors adn pd-1 inhibitors
SG11201808196UA (en) Neoantigens and methods of their use
SG11201908719QA (en) Biomarkers and car t cell therapies with enhanced efficacy
SG11201810983PA (en) Novel heterocyclic derivatives useful as shp2 inhibitors
SG11201808907PA (en) Inhibitors of activin receptor-like kinase
SG11201907840RA (en) Fused imidazo-piperidine jak inhibitors
SG11201805044WA (en) Compounds useful as kinase inhibitors
SG11201803920TA (en) Compounds and compositions useful for treating disorders related to ntrk
SG11201808678QA (en) Macrocyclic inhibitors of the pd-1/pd-l1 and cd80/pd-l1 protein/protein interactions
SG11201808990QA (en) Compositions for topical application of compounds
SG11201900480YA (en) Anti-tim-3 antibodies
SG11201805300QA (en) Heterocyclic compounds as immunomodulators
SG11201807426WA (en) Immunomodulators
SG11201907451XA (en) Substituted imidazo-quinolines as nlrp3 modulators
SG11201804098TA (en) Purinones as ubiquitin-specific protease 1 inhibitors
SG11201805645QA (en) Lsd1 inhibitors
SG11201810927QA (en) Pd-l1-specific antibodies and methods of using the same
SG11201806251WA (en) Methods for treating er+, her2-, hrg+ breast cancer using combination therapies comprising an anti-erbb3 antibody
SG11201809751XA (en) Egfr inhibitor compounds
SG11201806282XA (en) High-throughput identification of patient-specific neoepitopes as therapeutic targets for cancer immunotherapies
SG11201908326YA (en) Methods of treating neurodegenerative diseases
SG11201908602UA (en) Combination therapy for the treatment of solid and hematological cancers