JP2017538677A5 - - Google Patents

Download PDF

Info

Publication number
JP2017538677A5
JP2017538677A5 JP2017524423A JP2017524423A JP2017538677A5 JP 2017538677 A5 JP2017538677 A5 JP 2017538677A5 JP 2017524423 A JP2017524423 A JP 2017524423A JP 2017524423 A JP2017524423 A JP 2017524423A JP 2017538677 A5 JP2017538677 A5 JP 2017538677A5
Authority
JP
Japan
Prior art keywords
optionally substituted
cancer
alkyl
therapeutic agent
compound
Prior art date
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.)
Granted
Application number
JP2017524423A
Other languages
English (en)
Japanese (ja)
Other versions
JP6762299B2 (ja
JP2017538677A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2015/059316 external-priority patent/WO2016073774A2/en
Publication of JP2017538677A publication Critical patent/JP2017538677A/ja
Publication of JP2017538677A5 publication Critical patent/JP2017538677A5/ja
Application granted granted Critical
Publication of JP6762299B2 publication Critical patent/JP6762299B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2017524423A 2014-11-05 2015-11-05 免疫調節剤 Active JP6762299B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201462075678P 2014-11-05 2014-11-05
US62/075,678 2014-11-05
PCT/US2015/059316 WO2016073774A2 (en) 2014-11-05 2015-11-05 Immunoregulatory agents

Publications (3)

Publication Number Publication Date
JP2017538677A JP2017538677A (ja) 2017-12-28
JP2017538677A5 true JP2017538677A5 (cg-RX-API-DMAC7.html) 2018-11-22
JP6762299B2 JP6762299B2 (ja) 2020-09-30

Family

ID=55910037

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2017524423A Active JP6762299B2 (ja) 2014-11-05 2015-11-05 免疫調節剤

Country Status (23)

Country Link
US (3) US20180325889A1 (cg-RX-API-DMAC7.html)
EP (1) EP3215142B1 (cg-RX-API-DMAC7.html)
JP (1) JP6762299B2 (cg-RX-API-DMAC7.html)
KR (1) KR102647639B1 (cg-RX-API-DMAC7.html)
CN (1) CN106999450B (cg-RX-API-DMAC7.html)
AR (1) AR102537A1 (cg-RX-API-DMAC7.html)
AU (1) AU2015342944A1 (cg-RX-API-DMAC7.html)
BR (1) BR112017007782A2 (cg-RX-API-DMAC7.html)
CA (1) CA2964297A1 (cg-RX-API-DMAC7.html)
CL (1) CL2017001126A1 (cg-RX-API-DMAC7.html)
CO (1) CO2017005218A2 (cg-RX-API-DMAC7.html)
EA (1) EA201790998A1 (cg-RX-API-DMAC7.html)
ES (1) ES2867748T3 (cg-RX-API-DMAC7.html)
IL (1) IL252010A0 (cg-RX-API-DMAC7.html)
MA (2) MA44549A1 (cg-RX-API-DMAC7.html)
MX (1) MX2017005729A (cg-RX-API-DMAC7.html)
PE (1) PE20171623A1 (cg-RX-API-DMAC7.html)
PH (1) PH12017500604A1 (cg-RX-API-DMAC7.html)
SG (1) SG11201702827VA (cg-RX-API-DMAC7.html)
TN (1) TN2017000165A1 (cg-RX-API-DMAC7.html)
TW (1) TW201630866A (cg-RX-API-DMAC7.html)
UY (1) UY36391A (cg-RX-API-DMAC7.html)
WO (1) WO2016073774A2 (cg-RX-API-DMAC7.html)

Families Citing this family (76)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB201311891D0 (en) 2013-07-03 2013-08-14 Glaxosmithkline Ip Dev Ltd Novel compound
GB201311888D0 (en) 2013-07-03 2013-08-14 Glaxosmithkline Ip Dev Ltd Novel compounds
US20180228907A1 (en) 2014-04-14 2018-08-16 Arvinas, Inc. Cereblon ligands and bifunctional compounds comprising the same
EP3151820A4 (en) 2014-06-06 2017-11-22 Flexus Biosciences, Inc. Immunoregulatory agents
AR102537A1 (es) 2014-11-05 2017-03-08 Flexus Biosciences Inc Agentes inmunomoduladores
MX2017005462A (es) 2014-11-05 2017-07-28 Flexus Biosciences Inc Agentes inmunorreguladores.
UY36390A (es) * 2014-11-05 2016-06-01 Flexus Biosciences Inc Compuestos moduladores de la enzima indolamina 2,3-dioxigenasa (ido), sus métodos de síntesis y composiciones farmacéuticas que los contienen
US10292951B2 (en) 2015-09-01 2019-05-21 First Wave Bio, Inc. Methods and compositions for treating conditions associated with an abnormal inflammatory responses
CN109414421A (zh) * 2016-05-04 2019-03-01 百时美施贵宝公司 吲哚胺2,3-双加氧酶的抑制剂及其使用方法
CN109414420A (zh) 2016-05-04 2019-03-01 百时美施贵宝公司 吲哚胺2,3-双加氧酶的抑制剂及其使用方法
JP2019522627A (ja) 2016-05-04 2019-08-15 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company インドールアミン2,3−ジオキシゲナーゼ阻害剤およびその使用方法
EP3452451A4 (en) 2016-05-04 2019-11-13 Bristol-Myers Squibb Company INDOLEAMINE 2,3-DIOXYGENASE INHIBITORS AND METHODS OF USE
JP2019516681A (ja) 2016-05-04 2019-06-20 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company インドールアミン2,3−ジオキシゲナーゼ阻害剤およびその使用方法
AR108586A1 (es) * 2016-06-10 2018-09-05 Lilly Co Eli Compuestos de 2,3-dihidro-1h-indol
WO2018024188A1 (zh) * 2016-08-02 2018-02-08 上海迪诺医药科技有限公司 多环化合物、其制备方法、药物组合物及应用
CN107674029A (zh) * 2016-08-02 2018-02-09 上海迪诺医药科技有限公司 多环化合物、其药物组合物及应用
EP3505517A4 (en) 2016-08-23 2020-01-15 Beijing InnoCare Pharma Tech Co., Ltd. Fused heterocyclic derivative, preparation method therefor and medical use thereof
JP2019528300A (ja) * 2016-08-26 2019-10-10 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company インドールアミン2,3−ジオキシゲナーゼの阻害剤およびその使用方法
EP3515914A4 (en) 2016-09-24 2020-04-15 BeiGene, Ltd. NEW IMIDAZO [1,5-A] PYRIDINES SUBSTITUTED IN POSITION 5 OR 8 AS INDOLEAMINE AND / OR TRYPTOPHANE 2,3-DIOXYGENASES
WO2018058123A1 (en) * 2016-09-26 2018-03-29 Advantagene, Inc. Methods of treating tim-3 elevation
SG10201911243WA (en) 2016-12-22 2020-02-27 Calithera Biosciences Inc Compositions and methods for inhibiting arginase activity
CN110191709A (zh) * 2017-01-17 2019-08-30 德州大学系统董事会 可用作吲哚胺2,3-双加氧酶和/或色氨酸双加氧酶抑制剂的化合物
WO2018209049A1 (en) 2017-05-12 2018-11-15 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
IL271601B2 (en) * 2017-06-30 2024-05-01 Bristol Myers Squibb Co Amorphous and crystalline forms of ido inhibitors
IL271233B (en) * 2017-06-30 2022-09-01 Bristol Myers Squibb Co Substituted quinolinylcyclohexylpropanamide compounds and improved methods for their preparation
WO2019057123A1 (zh) 2017-09-20 2019-03-28 杭州英创医药科技有限公司 作为ido抑制剂和/或ido-hdac双重抑制剂的多环化合物
US11351163B2 (en) 2017-09-29 2022-06-07 Bristol-Myers Squibb Company Compositions and methods of treating cancer
US11319283B2 (en) 2017-10-09 2022-05-03 Merck Sharp & Dohme Corp. Substituted cyclobutylbenzene compounds as indoleamine 2,3-dioxygenase (IDO) inhibitors
US11203592B2 (en) 2017-10-09 2021-12-21 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
US11111232B2 (en) 2017-10-09 2021-09-07 Merck Sharp & Dohme Corp. Substituted cyclobutylpyridine and cyclobutylpyrimidine compounds as indoleamine 2,3-dioxygenase (IDO) inhibitors
WO2019074822A1 (en) 2017-10-09 2019-04-18 Bristol-Myers Squibb Company INDOLEAMINE 2,3-DIOXYGENASE INHIBITORS AND METHODS OF USE
WO2019078968A2 (en) 2017-10-18 2019-04-25 Angex Pharmaceutical, Inc. CYCLIC COMPOUNDS AS IMMUNOMODULATORS
TWI780246B (zh) 2017-10-27 2022-10-11 德商百靈佳殷格翰國際股份有限公司 Trpc 6抑制劑
EP3720843A1 (en) * 2017-12-05 2020-10-14 GlaxoSmithKline Intellectual Property Development Limited Modulators of indoleamine 2,3-dioxygenase
CN109928921A (zh) * 2017-12-18 2019-06-25 成都华健未来科技有限公司 Ido抑制剂
CN109956937A (zh) * 2017-12-22 2019-07-02 上海海雁医药科技有限公司 N-(2-环己基乙基)甲酰胺衍生物、其制法与医药上的用途
CN109956929B (zh) * 2017-12-22 2023-09-19 上海迪诺医药科技有限公司 杂环衍生物、其制备方法、药物组合物及应用
WO2019120256A1 (zh) * 2017-12-22 2019-06-27 上海迪诺医药科技有限公司 五元杂芳环衍生物、其药物组合物及应用
CN109574988B (zh) * 2017-12-25 2022-01-25 成都海博锐药业有限公司 一种化合物及其用途
CN111587116A (zh) 2018-01-05 2020-08-25 迪克纳制药公司 降低β-连环蛋白和IDO表达以加强免疫疗法
US11447449B2 (en) 2018-01-05 2022-09-20 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
KR20200108298A (ko) * 2018-01-10 2020-09-17 리커리엄 아이피 홀딩스, 엘엘씨 벤즈아미드 화합물
WO2019141095A1 (zh) * 2018-01-19 2019-07-25 四川科伦博泰生物医药股份有限公司 脒类和胍类衍生物、其制备方法及其在医药上的应用
CN110066271B (zh) * 2018-01-23 2023-04-07 上海迪诺医药科技有限公司 吡咯衍生物、其制备方法、药物组合物及应用
CN110066236B (zh) * 2018-01-24 2023-03-24 上海迪诺医药科技有限公司 1h-吡咯衍生物、其制备方法、药物组合物及应用
CN110092750B (zh) * 2018-01-29 2023-07-21 北京诺诚健华医药科技有限公司 五氟硫烷基取代的酰胺类化合物、其制备方法及其在医药学上的应用
CN111868032B (zh) * 2018-02-11 2021-09-03 基石药业(苏州)有限公司 犬尿氨酸通路抑制剂
CN110156656B (zh) * 2018-02-13 2023-04-07 上海迪诺医药科技有限公司 五元杂芳环衍生物、其制备方法、药物组合物及应用
CN118084940A (zh) 2018-02-13 2024-05-28 吉利德科学公司 Pd-1/pd-l1抑制剂
MX2020008984A (es) * 2018-02-28 2020-12-09 Dart Neuroscience Llc Compuestos de ciclohexilo sustituido como inhibidores de nop.
AU2019232437A1 (en) 2018-03-07 2020-10-08 Bayer Aktiengesellschaft Identification and use of ERK5 inhibitors
WO2019179369A1 (zh) * 2018-03-19 2019-09-26 四川科伦博泰生物医药股份有限公司 含环化合物、其制备方法及其在医药上的应用
CN110357813A (zh) * 2018-04-09 2019-10-22 信达生物制药(苏州)有限公司 一种新型吲哚胺2,3-双加氧酶抑制剂及其制备方法和用途
AU2019255750B2 (en) 2018-04-19 2021-10-21 Gilead Sciences, Inc. PD-1/PD-L1 inhibitors
CN110498769A (zh) * 2018-05-17 2019-11-26 南京药捷安康生物科技有限公司 Ido抑制剂与应用
CN110105275B (zh) * 2018-05-28 2020-12-29 上海海雁医药科技有限公司 酰胺类衍生物、其制法与医药上的用途
KR102651420B1 (ko) * 2018-07-06 2024-03-28 길리애드 사이언시즈, 인코포레이티드 치료 헤테로시클릭 화합물
PE20210642A1 (es) 2018-07-13 2021-03-23 Gilead Sciences Inc Inhibidores de pd-1/pd-l1
US11046649B2 (en) 2018-07-17 2021-06-29 Board Of Regents, The University Of Texas System Compounds useful as inhibitors of indoleamine 2,3-dioxygenase and/or tryptophan dioxygenase
US12059420B2 (en) 2018-07-23 2024-08-13 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
WO2020023356A1 (en) 2018-07-23 2020-01-30 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
GB201813312D0 (en) * 2018-08-15 2018-09-26 Modern Biosciences Ltd Compounds and their therapeutic use
US11253525B2 (en) 2018-08-29 2022-02-22 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
US10959986B2 (en) 2018-08-29 2021-03-30 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
CN112955435B (zh) 2018-10-24 2024-09-06 吉利德科学公司 Pd-1/pd-l1抑制剂
JP7758664B2 (ja) * 2019-10-30 2025-10-22 バイオジェン・エムエイ・インコーポレイテッド ブルトン型チロシンキナーゼに対する阻害剤としての縮合型二複素環
CN110878013B (zh) * 2019-12-13 2023-04-28 西安瑞联新材料股份有限公司 (反,反)-4-乙烯基-4’-[(e)-1-丙烯基]-双环己烷的合成方法
US10980756B1 (en) 2020-03-16 2021-04-20 First Wave Bio, Inc. Methods of treatment
WO2021230710A1 (ko) * 2020-05-15 2021-11-18 (주)신테카바이오 신규 ido/tdo 억제제, 그의 항암 용도, 그의 항암 병용 요법
KR102653960B1 (ko) * 2020-07-23 2024-04-03 의료법인 성광의료재단 암 치료를 위한 면역체크포인트 억제제의 병용 요법
WO2022034146A1 (en) 2020-08-13 2022-02-17 Boehringer Ingelheim International Gmbh Treatment of cognitive impairement associated with schizophrenia
WO2022078927A1 (en) 2020-10-13 2022-04-21 Boehringer Ingelheim International Gmbh Process of reworking
JP2024503280A (ja) * 2020-12-29 2024-01-25 レボリューション メディシンズ インコーポレイテッド Sos1阻害剤及びその使用
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
KR20240019340A (ko) * 2021-06-11 2024-02-14 뉴로내슨트, 아이엔씨. 헤테로시클릭 유형의 친유성 소분자 치료의 지질 제제를 위한 방법 및 조성물

Family Cites Families (94)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3169188B2 (ja) * 1991-01-31 2001-05-21 杏林製薬株式会社 カルバミン酸誘導体及びその製造方法
AU666040B2 (en) 1992-10-28 1996-01-25 Bayer Aktiengesellschaft Substituted 1-H-3-aryl-pyrrolidine-2,4-dione derivatives
DE4239151A1 (de) * 1992-11-20 1994-05-26 Thomae Gmbh Dr K N,N-Disubstituierte Arylcycloalkylamine, deren Salze, diese Verbindungen enthaltende Arzneimittel und deren Verwendung sowie Verfahren zu ihrer Herstellung
GB9411099D0 (en) 1994-06-03 1994-07-27 Wyeth John & Brother Ltd Piperazine derivatives
US6451840B1 (en) 1997-12-05 2002-09-17 Medical College Of Georgia Research Institute, Inc. Regulation of T cell-mediated immunity by tryptophan
CO5150225A1 (es) 1999-03-19 2002-04-29 Merck Sharp & Dohme Derivados del tetrahidropirano y su uso como agentes terapeuticos
WO2000071171A2 (en) * 1999-05-21 2000-11-30 Wake Forest University Sigma-1 ligands for determining carcinoma proliferative status
US6291499B1 (en) * 1999-10-29 2001-09-18 Merck & Co., Inc. 2-cyclohexyl benzimidazole NMDA/NR2B antagonists
US20020002171A1 (en) * 2000-01-28 2002-01-03 Chalquest Richard R. Materials and methods for killing nematodes and nematode eggs
US6677336B2 (en) 2000-02-22 2004-01-13 Cv Therapeutics, Inc. Substituted piperazine compounds
AU2001261487A1 (en) 2000-06-01 2001-12-11 Warner Lambert Company Cyclohexylamine derivatives as subtype selective nmda receptor antagonists
CA2413579A1 (en) * 2000-06-23 2002-01-03 Eli Lilly And Company Methods and compounds for inhibiting mrp1
MXPA03002080A (es) * 2000-09-11 2003-06-24 Pfizer Prod Inc Derivados de resorcinol.
EP1318974A2 (en) 2000-09-21 2003-06-18 Pfizer Products Inc. Resorcinol derivatives
EP1217000A1 (en) * 2000-12-23 2002-06-26 Aventis Pharma Deutschland GmbH Inhibitors of factor Xa and factor VIIa
ATE425152T1 (de) * 2002-03-13 2009-03-15 Janssen Pharmaceutica Nv Aminocarbonylderivate als histone-deacetylase- inhibitoren
MY134200A (en) * 2002-04-12 2007-11-30 Kowa Co Method for treating cancer
US20040029887A1 (en) 2002-05-23 2004-02-12 Bhatia Pramila A. Acetamides and benzamides that are useful in treating sexual dysfunction
NZ539952A (en) * 2002-11-22 2008-05-30 Japan Tobacco Inc Fused bicyclic nitrogen-containing heterocyclic compounds for treating diabetes, obesity and syndrome X
AU2003300902A1 (en) * 2002-12-13 2004-07-09 Smithkline Beecham Corporation Piperidine derivatives as CCR5 antagonists
CN103265477B (zh) * 2003-02-26 2017-01-11 苏根公司 作为蛋白激酶抑制剂的氨基杂芳基化合物
WO2004093871A1 (en) 2003-03-27 2004-11-04 Lankenau Institute For Medical Research Novel methods for the treatment of cancer
US7598287B2 (en) 2003-04-01 2009-10-06 Medical College Of Georgia Research Institute, Inc. Use of inhibitors of indoleamine-2,3-dioxygenase in combination with other therapeutic modalities
AU2004291147A1 (en) * 2003-11-13 2005-06-02 Ambit Biosciences Corporation Urea derivatives as kinase modulators
US20070167452A1 (en) 2004-02-11 2007-07-19 Pfizer, Inc. Therapeutic amide derivatives
DE102004023507A1 (de) * 2004-05-10 2005-12-01 Grünenthal GmbH Substituierte Cyclohexylessigsäure-Derivate
DE102004039789A1 (de) * 2004-08-16 2006-03-02 Sanofi-Aventis Deutschland Gmbh Arylsubstituierte polycyclische Amine, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
TWI380996B (zh) 2004-09-17 2013-01-01 Hoffmann La Roche 抗ox40l抗體
DK1866339T3 (da) 2005-03-25 2013-09-02 Gitr Inc GTR-bindende molekyler og anvendelser heraf
TW200720231A (en) * 2005-04-21 2007-06-01 Dainippon Sumitomo Pharma Co An n-substituted phenylacetamide derivative and a pharmaceutical composition thereof
CN101212967A (zh) 2005-05-10 2008-07-02 因塞特公司 吲哚胺2,3-双加氧酶调节剂及其用法
WO2007044085A2 (en) * 2005-05-19 2007-04-19 Xenon Pharmaceuticals Inc. Heteroaryl compounds and their uses as therapeutic agents
US20070004763A1 (en) * 2005-06-10 2007-01-04 Nand Baindur Aminoquinoline and aminoquinazoline kinase modulators
CN104356236B (zh) 2005-07-01 2020-07-03 E.R.施贵宝&圣斯有限责任公司 抗程序性死亡配体1(pd-l1)的人单克隆抗体
CN102936250B (zh) * 2005-11-17 2014-07-09 Osi医药有限责任公司 稠合双环mTOR抑制剂
WO2007082079A2 (en) * 2006-01-12 2007-07-19 The Scripps Research Institute Piperidine amide derivatives as protein kinase inhibitors
US20070203140A1 (en) * 2006-02-09 2007-08-30 Combs Andrew P N-hydroxyguanidines as modulators of indoleamine 2,3-dioxygenase
JP5372737B2 (ja) * 2006-03-13 2013-12-18 オーエスアイ・フアーマシユーテイカルズ・エル・エル・シー Egfrキナーゼ阻害剤およびegfrキナーゼ阻害剤の効果に対し腫瘍細胞を感作する薬剤を用いる併用治療
WO2007109288A2 (en) 2006-03-20 2007-09-27 Xytis Inc. Enantiomerically pure r-etifoxine, pharmaceutical compositions thereof and methods of their use
WO2007137107A2 (en) * 2006-05-19 2007-11-29 Abbott Laboratories Inhibitors of diacylglycerol o-acyltransferase type 1 enzyme
AU2007267470B2 (en) 2006-06-01 2012-09-20 Sanofi-Aventis Spirocyclic nitriles as protease inhibitors
US20080119491A1 (en) 2006-09-19 2008-05-22 Incyte Corporation Amidinoheterocycles as modulators of indoleamine 2,3-dioxygenase
EP2094704A4 (en) 2006-11-06 2010-12-08 Neurogen Corp CIS-CYCLOHEXYL SUBSTITUTED PYRIMIDINONE DERIVATIVES
CA2672373C (en) 2006-12-19 2011-08-30 Pfizer Products Inc. Nicotinamide derivatives as inhibitors of h-pgds and their use for treating prostaglandin d2 mediated diseases
EP2121580A2 (en) * 2006-12-26 2009-11-25 Amgen Inc. N-cyclohexyl benzamides and benzeneacetamides as inhibitors of 11-beta-hydroxysteroid dehydrogenases
MY151953A (en) * 2006-12-27 2014-07-31 Sanofi Aventis Cycloalkylamine substituted isoquinoline derivatives
US20100249111A1 (en) * 2007-04-26 2010-09-30 Avalon Pharmaceuticals Multi-ring compounds and uses thereof
EP1987839A1 (en) 2007-04-30 2008-11-05 I.N.S.E.R.M. Institut National de la Sante et de la Recherche Medicale Cytotoxic anti-LAG-3 monoclonal antibody and its use in the treatment or prevention of organ transplant rejection and autoimmune disease
JP2010530417A (ja) * 2007-06-20 2010-09-09 メルク・シャープ・エンド・ドーム・コーポレイション ベンゾオキサゾールアリールアミドから誘導されたcetp阻害剤
US20090023773A1 (en) * 2007-06-27 2009-01-22 Painceptor Pharma Corporation Compositions and methods for modulating gated ion channels
US20090274698A1 (en) * 2007-07-06 2009-11-05 Shripad Bhagwat Combination anti-cancer therapy
AU2008275589B2 (en) 2007-07-12 2013-11-21 Gitr, Inc. Combination therapies employing GITR binding molecules
EP2044949A1 (en) 2007-10-05 2009-04-08 Immutep Use of recombinant lag-3 or the derivatives thereof for eliciting monocyte immune response
EP2203058A4 (en) * 2007-10-16 2011-08-31 Univ Northeastern METHODS AND COMPOUNDS FOR MODULATING CANNABINOID ACTIVITY
EA019882B1 (ru) * 2008-03-18 2014-07-30 Арена Фармасьютикалз, Инк. Модуляторы рецептора простациклина (pgi2), пригодные для лечения связанных с ним расстройств
PE20121313A1 (es) 2008-03-27 2012-10-07 Gruenenthal Chemie Derivados de 4-aminociclohexano sustituidos
US20110039860A1 (en) * 2008-05-07 2011-02-17 Cangming Yang Soluble epoxide hydrolase inhibitors, compositions containing such compounds and methods of treatment
CN104042611B (zh) 2008-07-08 2019-05-14 因塞特控股公司 作为吲哚胺2,3-双加氧酶的抑制剂的1,2,5-噁二唑
US8273900B2 (en) 2008-08-07 2012-09-25 Novartis Ag Organic compounds
AR072999A1 (es) 2008-08-11 2010-10-06 Medarex Inc Anticuerpos humanos que se unen al gen 3 de activacion linfocitaria (lag-3) y los usos de estos
TW202442680A (zh) 2008-12-09 2024-11-01 美商建南德克公司 抗pd-l1抗體及其於增進t細胞功能之用途
RU2505540C2 (ru) 2008-12-23 2014-01-27 Эббви Инк. Антивирусные соединения
CA2750635A1 (en) * 2009-02-23 2010-08-26 Merck Canada Inc. Heterocyclic derivatives as inhibitors of stearoyl-coenzyme a delta-9 desaturase
IN2012DN01920A (cg-RX-API-DMAC7.html) 2009-09-03 2015-07-24 Schering Corp
CN105218672A (zh) 2009-12-10 2016-01-06 霍夫曼-拉罗奇有限公司 优先结合人csf1r胞外域4的抗体及其用途
EP2982380B1 (en) 2010-03-04 2021-09-01 MacroGenics, Inc. Antibodies reactive with b7-h3, immunologically active fragments thereof and uses thereof
CN102918061B (zh) 2010-03-05 2016-06-08 霍夫曼-拉罗奇有限公司 针对人csf-1r的抗体及其用途
RU2617971C2 (ru) 2010-03-05 2017-04-28 Ф.Хоффманн-Ля Рош Аг Антитела против csf-1r человека и их применение
JP5266430B2 (ja) 2010-04-24 2013-08-21 ヴィアメット ファーマスーティカルズ,インコーポレイテッド 金属酵素阻害化合物
CN112480256A (zh) 2010-05-04 2021-03-12 戊瑞治疗有限公司 结合csf1r的抗体
US8658603B2 (en) 2010-06-16 2014-02-25 The Regents Of The University Of Michigan Compositions and methods for inducing an immune response
DK2614082T3 (en) 2010-09-09 2018-11-26 Pfizer 4-1BB BINDING MOLECULES
US9446763B2 (en) 2010-12-23 2016-09-20 Magna Powertrain Inc. Controlled gerotor actuated pre-trans parallel hybrid
PT2699264T (pt) 2011-04-20 2018-05-23 Medimmune Llc Anticorpos e outras moléculas que ligam b7-h1 e pd-1
US9586928B2 (en) * 2011-05-16 2017-03-07 The Scripps Research Institute Modulators of the nuclear hormone receptor ROR
US8993757B2 (en) * 2011-09-22 2015-03-31 Merck Sharp & Dohme B.V. N-piperidin-4-yl derivatives
TW201326154A (zh) 2011-11-28 2013-07-01 拜耳知識產權公司 作為ep2受體拮抗劑之新穎2h-吲唑
MX349096B (es) 2011-11-28 2017-07-11 Merck Patent Gmbh Anticuerpos anti-pd-l1 y sus usos.
WO2013086002A1 (en) * 2011-12-05 2013-06-13 Cellworks Research India Private Limited Compositions, process of preparation of said compositions and method of treating cancer
WO2013119716A1 (en) 2012-02-06 2013-08-15 Genentech, Inc. Compositions and methods for using csf1r inhibitors
AR090263A1 (es) 2012-03-08 2014-10-29 Hoffmann La Roche Terapia combinada de anticuerpos contra el csf-1r humano y las utilizaciones de la misma
JP2015517490A (ja) 2012-05-11 2015-06-22 ファイブ プライム セラピューティックス インコーポレイテッド コロニー刺激因子1受容体(csf1r)を結合させる抗体を用いて状態を治療する方法
HRP20161745T1 (hr) * 2012-06-26 2017-02-24 Bayer Pharma Aktiengesellschaft N-[4-(kinolin-4-iloksi)cikloheksil(methil)](hetero)arilkarboksamidi kao antagonisti receptora androgena, njihova proizvodnja i uporaba kao medicinskih proizvoda
UY34887A (es) 2012-07-02 2013-12-31 Bristol Myers Squibb Company Una Corporacion Del Estado De Delaware Optimización de anticuerpos que se fijan al gen de activación de linfocitos 3 (lag-3) y sus usos
US10449182B2 (en) * 2012-07-06 2019-10-22 The Regents Of The University Of California Sorafenib derivatives as p21 inhibitors
CN104704002B (zh) 2012-08-30 2022-05-10 安姆根有限公司 使用单纯疱疹病毒和免疫检查点抑制剂治疗黑色素瘤的方法
BR112015004426A2 (pt) 2012-08-31 2018-08-28 Five Prime Therapeutics, Inc. método para reduzir o nível, tratar uma condição, tratar uma condição inflamatória, tratar distúrbio de cd16+, tratar um respondente inadequado de metotrexate, tratar um respondente inadequado de inibidor de tnf, indentificar um sujeito, predizer responsividade e métodos para tratar uma condição inflamatória
AU2014235750B2 (en) 2013-03-15 2018-05-17 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase (IDO)
US12433920B2 (en) * 2013-03-29 2025-10-07 Biomed Valley Discoveries, Inc. C. novyi for the treatment of solid tumors in non-human animals
EP3151820A4 (en) * 2014-06-06 2017-11-22 Flexus Biosciences, Inc. Immunoregulatory agents
GB201419579D0 (en) 2014-11-03 2014-12-17 Iomet Pharma Ltd Pharmaceutical compound
MX2017005462A (es) 2014-11-05 2017-07-28 Flexus Biosciences Inc Agentes inmunorreguladores.
UY36390A (es) 2014-11-05 2016-06-01 Flexus Biosciences Inc Compuestos moduladores de la enzima indolamina 2,3-dioxigenasa (ido), sus métodos de síntesis y composiciones farmacéuticas que los contienen
AR102537A1 (es) 2014-11-05 2017-03-08 Flexus Biosciences Inc Agentes inmunomoduladores

Similar Documents

Publication Publication Date Title
JP2017538677A5 (cg-RX-API-DMAC7.html)
JP2017537080A5 (cg-RX-API-DMAC7.html)
JP2017538678A5 (cg-RX-API-DMAC7.html)
KR102566924B1 (ko) 케모카인 수용체 조절제 및 이의 용도
RU2015118647A (ru) Аминопиримидиновые соединения в качестве ингибиторов содержащих т790м мутантных egfr
JP2017525753A5 (cg-RX-API-DMAC7.html)
JP2014525464A5 (cg-RX-API-DMAC7.html)
JP2019529500A5 (cg-RX-API-DMAC7.html)
JP2015508103A5 (cg-RX-API-DMAC7.html)
JP2015531371A5 (cg-RX-API-DMAC7.html)
JP2019516766A5 (cg-RX-API-DMAC7.html)
JP2020517616A5 (cg-RX-API-DMAC7.html)
JP2017509689A5 (cg-RX-API-DMAC7.html)
JP2015503625A5 (cg-RX-API-DMAC7.html)
JP2013537203A5 (cg-RX-API-DMAC7.html)
JP2013518089A5 (cg-RX-API-DMAC7.html)
HRP20210291T1 (hr) Imunoregulatorna sredstva
HRP20171248T1 (hr) Amino-supstituirani imidazopiridazini
JP2018516238A5 (cg-RX-API-DMAC7.html)
JP2016503414A5 (cg-RX-API-DMAC7.html)
JP2015512398A5 (cg-RX-API-DMAC7.html)
JP2016533366A5 (cg-RX-API-DMAC7.html)
JP2016506916A5 (cg-RX-API-DMAC7.html)
JP2017508782A5 (cg-RX-API-DMAC7.html)
JP2013520443A5 (cg-RX-API-DMAC7.html)