JP2016518324A5 - - Google Patents

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Publication number
JP2016518324A5
JP2016518324A5 JP2016501372A JP2016501372A JP2016518324A5 JP 2016518324 A5 JP2016518324 A5 JP 2016518324A5 JP 2016501372 A JP2016501372 A JP 2016501372A JP 2016501372 A JP2016501372 A JP 2016501372A JP 2016518324 A5 JP2016518324 A5 JP 2016518324A5
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JP
Japan
Prior art keywords
optionally substituted
alkyl
aryl
pharmaceutically acceptable
cancer
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Legal status (The legal status 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 status listed.)
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Application number
JP2016501372A
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English (en)
Japanese (ja)
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JP2016518324A (ja
JP6313415B2 (ja
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Priority claimed from PCT/US2014/023877 external-priority patent/WO2014150646A1/en
Publication of JP2016518324A publication Critical patent/JP2016518324A/ja
Publication of JP2016518324A5 publication Critical patent/JP2016518324A5/ja
Application granted granted Critical
Publication of JP6313415B2 publication Critical patent/JP6313415B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2016501372A 2013-03-15 2014-03-12 Ido阻害剤 Active JP6313415B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201361787939P 2013-03-15 2013-03-15
US61/787,939 2013-03-15
PCT/US2014/023877 WO2014150646A1 (en) 2013-03-15 2014-03-12 Ido inhibitors

Publications (3)

Publication Number Publication Date
JP2016518324A JP2016518324A (ja) 2016-06-23
JP2016518324A5 true JP2016518324A5 (enExample) 2017-03-02
JP6313415B2 JP6313415B2 (ja) 2018-04-18

Family

ID=50391513

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2016501372A Active JP6313415B2 (ja) 2013-03-15 2014-03-12 Ido阻害剤

Country Status (19)

Country Link
US (1) US9624188B2 (enExample)
EP (1) EP2970114B1 (enExample)
JP (1) JP6313415B2 (enExample)
KR (1) KR20150129010A (enExample)
CN (1) CN105324362B (enExample)
AU (1) AU2014235816B2 (enExample)
BR (1) BR112015022462A8 (enExample)
CA (1) CA2907178A1 (enExample)
EA (1) EA028424B1 (enExample)
ES (1) ES2733546T3 (enExample)
HK (1) HK1220442A1 (enExample)
IL (1) IL241321A0 (enExample)
MA (1) MA38483A1 (enExample)
MX (1) MX2015012056A (enExample)
PE (1) PE20151594A1 (enExample)
PH (1) PH12015502028A1 (enExample)
SG (1) SG11201506920QA (enExample)
WO (1) WO2014150646A1 (enExample)
ZA (1) ZA201506796B (enExample)

Families Citing this family (49)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NO2694640T3 (enExample) 2011-04-15 2018-03-17
EA031470B1 (ru) * 2013-03-15 2019-01-31 Бристол-Майерс Сквибб Компани Ингибиторы ido
MX2015017486A (es) 2013-07-01 2016-03-21 Squibb Bristol Myers Co Inhibidores de indolamina 2,3-dioxigenasa (dio).
ES2707961T3 (es) * 2013-07-11 2019-04-08 Bristol Myers Squibb Co Inhibidores de IDO
RS60614B1 (sr) 2015-03-23 2020-08-31 Jounce Therapeutics Inc Antitela za icos
KR20170134981A (ko) * 2015-04-03 2017-12-07 브리스톨-마이어스 스큅 컴퍼니 암의 치료를 위한 인돌아민-2,3-디옥시게나제의 억제제
AU2016284812A1 (en) 2015-06-26 2018-02-15 Bristol-Myers Squibb Company IDO inhibitors
US10786547B2 (en) 2015-07-16 2020-09-29 Biokine Therapeutics Ltd. Compositions, articles of manufacture and methods for treating cancer
EP4659747A2 (en) 2015-07-24 2025-12-10 Lumos Pharma, Inc. Salts and prodrugs of 1-methyl-d-tryptophan
CN108368049A (zh) * 2015-09-24 2018-08-03 葛兰素史克知识产权开发有限公司 吲哚胺2,3-双加氧酶的调节剂
EP3359150A4 (en) * 2015-10-05 2019-11-06 Calithera Biosciences, Inc. COMBINATION THERAPY WITH GLUTAMINASE INHIBITORS AND IMMUNO-ONCOLOGICAL AGENTS
AU2016342269A1 (en) 2015-10-22 2018-03-29 Jounce Therapeutics, Inc. Gene signatures for determining icos expression
WO2017139414A1 (en) 2016-02-09 2017-08-17 Inventisbio Inc. Inhibitor of indoleamine-2,3-dioxygenase (ido)
WO2017140835A1 (en) 2016-02-19 2017-08-24 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods and pharmaceutical compositions for the treatment of obesity
JP6948345B2 (ja) * 2016-04-29 2021-10-13 イオメット ファーマ リミテッド インドールアミン2,3−ジオキシゲナーゼ及び/又はトリプトファン−2,3−ジオキシゲナーゼの阻害薬としての新規置換イミダゾピリジン化合物
EP3455220A1 (en) * 2016-05-12 2019-03-20 GlaxoSmithKline Intellectual Property Development Limited Modulators of indoleamine 2,3-dioxygenase
AR108586A1 (es) 2016-06-10 2018-09-05 Lilly Co Eli Compuestos de 2,3-dihidro-1h-indol
WO2018036414A1 (zh) * 2016-08-23 2018-03-01 北京诺诚健华医药科技有限公司 稠杂环类衍生物、其制备方法及其在医学上的应用
US10882856B2 (en) 2016-09-24 2021-01-05 Beigene, Ltd. 5 or 8-substituted imidazo [1,5-a] pyridines as selective inhibitors of indoleamine and/or tryptophane 2,3-dioxygenases
JP7623784B2 (ja) 2016-10-13 2025-01-29 ジュノー セラピューティクス インコーポレイテッド トリプトファン代謝経路調節剤を含む免疫療法の方法および組成物
HRP20211703T1 (hr) 2016-11-02 2022-02-04 Jounce Therapeutics, Inc. Protutijela protiv pd-1 i njihova upotreba
US11672771B2 (en) 2016-11-04 2023-06-13 Aximmune, Inc. Beta-alethine, immune modulators, and uses thereof
EP3558978A1 (en) 2016-12-20 2019-10-30 GlaxoSmithKline Intellectual Property Development Limited Modulators of indoleamine 2,3-dioxygenase
CN114989205A (zh) 2016-12-22 2022-09-02 卡里塞拉生物科学股份公司 用于抑制精氨酸酶活性的组合物和方法
CA3047002A1 (en) 2017-01-17 2018-07-26 Board Of Regents, The University Of Texas System Compounds useful as inhibitors of indoleamine 2,3-dioxygenase and/or tryptophan dioxygenase
US20200024351A1 (en) 2017-04-03 2020-01-23 Jounce Therapeutics, Inc. Compositions and Methods for the Treatment of Cancer
WO2019074748A1 (en) * 2017-10-09 2019-04-18 Merck Sharp & Dohme Corp. NOVEL SUBSTITUTED PHENYL-OXETANE AND PHENYLTETRAHYDROFURAN COMPOUNDS AS INHIBITORS OF INDOLEAMINE 2,3-DIOXYGENASE (IDO)
CN109836356B (zh) * 2017-11-24 2022-03-08 沈阳化工研究院有限公司 一种芳甲醚衍生物及其应用
EA202091540A1 (ru) 2017-12-22 2021-03-22 Джаунс Терапьютикс, Инк. Антитела к lilrb2
US11813280B2 (en) 2018-01-05 2023-11-14 Dicerna Pharmaceuticals, Inc. Reducing beta-catenin and IDO expression to potentiate immunotherapy
US11447449B2 (en) * 2018-01-05 2022-09-20 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
CN112703012A (zh) 2018-05-14 2021-04-23 震动疗法公司 治疗癌症的方法
WO2020018670A1 (en) 2018-07-17 2020-01-23 Board Of Regents, The University Of Texas System Compounds useful as inhibitors of indoleamine 2,3-dioxygenase and/or tryptophan dioxygenase
WO2020023356A1 (en) 2018-07-23 2020-01-30 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
US12059420B2 (en) 2018-07-23 2024-08-13 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
US20210353750A1 (en) 2018-10-18 2021-11-18 Jounce Therapeutics, Inc. Methods of Treating Cancer
US20210380942A1 (en) 2018-10-24 2021-12-09 Jounce Therapeutics, Inc. Methods and compositions for the treatment of cancer and infectious diseases
WO2020086943A1 (en) 2018-10-26 2020-04-30 Jounce Therapeutics, Inc. Methods of treating cancer
WO2020185739A1 (en) 2019-03-11 2020-09-17 Jounce Therapeutics, Inc. Anti-icos antibodies for the treatment of cancer
JP2022554270A (ja) 2019-11-05 2022-12-28 ジョンス セラピューティクス, インコーポレイテッド 抗pd-1抗体による癌を治療する方法
AU2020384481B2 (en) 2019-11-12 2025-12-11 Nammi Therapeutics, Inc. Formulated and/or co-formulated liposome compositions containing IDO antagonist prodrugs useful in the treatment of cancer and methods thereof
WO2021102618A1 (en) * 2019-11-25 2021-06-03 InventisBio Co., Ltd. Novel salts of indoleamine 2,3-dioxygenase inhibitors
JP2023510847A (ja) 2020-01-13 2023-03-15 ジャウンス セラピューティックス, インク. 癌の治療方法
CN111153846B (zh) * 2020-01-17 2021-08-31 中国药科大学 吡咯类化合物、其制备方法和药物组合物与用途
TWI890283B (zh) 2020-02-14 2025-07-11 美商基利科學股份有限公司 結合ccr8之抗體及融合蛋白及其用途
US11839659B2 (en) 2020-07-02 2023-12-12 Northwestern University Proteolysis-targeting chimeric molecules (PROTACs) that induce degradation of indoleamine 2,3-dioxygenase (IDO) protein
MX2023010371A (es) 2021-03-05 2024-02-12 Univ Basel Composiciones para el tratamiento de enfermedades o condiciones asociadas al veb.
EP4052705A1 (en) 2021-03-05 2022-09-07 Universität Basel Vizerektorat Forschung Compositions for the treatment of ebv associated diseases or conditions
WO2023235699A1 (en) 2022-05-31 2023-12-07 Jounce Therapeutics, Inc. Antibodies to lilrb4 and uses thereof

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5447957A (en) * 1994-06-02 1995-09-05 Smithkline Beecham Corp. Anti-inflammatory compounds
JP4618845B2 (ja) 1999-06-09 2011-01-26 杏林製薬株式会社 ヒトペルオキシゾーム増殖薬活性化受容体(PPAR)αアゴニストとしての置換フェニルプロピオン酸誘導体
WO2002046146A1 (fr) 2000-12-05 2002-06-13 Kyorin Pharmaceutical Co., Ltd. Derives d'acide carboxylique substitues
EP1505966A4 (en) 2002-05-10 2006-08-30 Bristol Myers Squibb Co 1,1-DISUBSTITUTED CYCLOALKYL DERIVATIVES AS FACTOR XA HEMMER
US7056925B2 (en) * 2002-08-13 2006-06-06 Abbott Laboratories Urea kinase inhibitors
US20040034038A1 (en) * 2002-08-13 2004-02-19 Goaquan Li Urea kinase inhibitors
AU2005245389A1 (en) * 2004-05-12 2005-12-01 Bristol-Myers Squibb Company Urea antagonists of P2Y1 receptor useful in the treatment of thrombotic conditions
WO2006049941A2 (en) * 2004-10-27 2006-05-11 Neurogen Corporation Diaryl ureas as cb1 antagonists
GB0613674D0 (en) * 2006-07-10 2006-08-16 Proskelia Sas Derivatives of urea and related diamines, methods for their manufacture, and uses therefor
CA2722159C (en) 2008-04-24 2016-04-05 Newlink Genetics Corporation Substituted phenylimidazole compounds and their use as ido inhibitors
EA031470B1 (ru) 2013-03-15 2019-01-31 Бристол-Майерс Сквибб Компани Ингибиторы ido

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