JP2017538677A5 - - Google Patents

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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
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Claims (11)

  1. 式(I):
    Figure 2017538677
    (I)
    [式中、
    下付き記号nは、1または0であり;
    Aは、−C(O)−、−NH−、−SO−、−CH−、または−CHR−であり;
    Bは、結合、−C(O)−、−NH−、−CH−、または−CHR−であり;
    Tは、結合、−CH−、−NH−、−O−、−OCH−、−C(O)CH−、または−CR−であって;
    Aが−NH−であり、Bが−C(O)−である場合、Tは、−C(R)(R)−以外であり;
    Dは、NまたはC(R)であり;
    Eは、NまたはC(R)であり;
    Vは、結合、−O−、または−C(R5aであり;
    Gは、適宜置換されていてもよいアリール、適宜置換されていてもよいヘテロアリール、または適宜置換されていてもよい9もしくは10員縮合二環式ヘテロアリールであり;
    がJとして同定される環の頂点に結合している場合、Jは、CH、NまたはC(R)であり;
    およびRは、独立して、水素、ハロゲン、適宜置換されていてもよいC−Cハロアルキル、適宜置換されていてもよいC−Cシクロアルキル、適宜置換されていてもよい3もしくは6員シクロヘテロアルキル、適宜置換されていてもよいフェニル、適宜置換されていてもよいヘテロアリール、適宜置換されていてもよいC−Cアルキル、適宜置換されていてもよいC−Cアルコキシ、CN、SONH、NHSOCH、NHSOCF、OCF、SOCH、SOCF、またはCONHであり、RおよびRが、フェニル環の隣接する頂点にある場合、それらは、一緒になって、O、NおよびSから独立して選択される1もしくは2つの環の頂点を有する5もしくは6員シクロヘテロアルキル環を形成していてもよく、前記シクロヘテロアルキル環は、フルオロおよびC−Cアルキルから選択される1〜3個の基で適宜置換されていてもよく;
    およびRは、独立して、水素、適宜置換されていてもよいC−Cアルキル、適宜置換されていてもよいC−Cハロアルキル、フッ素、OH、CN、COH、C(O)NH、N(R5a、適宜置換されていてもよい−O−C−Cアルキル、−(CR−OH、−(CR−COH、−(CR−C(O)NH、−(CR−C(O)NHR5a、−(CRN(R5a、−NH(CRCOH、または−NH(CR−C(O)NHであり;
    各Rは、独立して、H、F、OH、適宜置換されていてもよいC−Cアルキル、または適宜置換されていてもよい−O−C−Cアルキルであり;
    各R5aは、独立して、H、または適宜置換されていてもよいC−Cアルキルであり;
    は、H、OH、F、適宜置換されていてもよいC−Cアルキル、適宜置換されていてもよい−O−C−Cアルキル、または−N(R5aであり;ならびに
    各mは、独立して、1、2、または3である]
    で示される化合物またはその医薬的に許容される塩、水和物もしくは溶媒和物。
  2. 式:
    Figure 2017538677
    (Ia)
    Figure 2017538677
    (Ia1)
    Figure 2017538677
    (Ia2)
    Figure 2017538677
    Figure 2017538677
    Figure 2017538677
    Figure 2017538677
    Figure 2017538677
    (Ia3)
    Figure 2017538677
    Figure 2017538677
    Figure 2017538677
    Figure 2017538677
    Figure 2017538677
    (Ib)
    Figure 2017538677
    (Ic)
    Figure 2017538677
    (Id)
    Figure 2017538677
    (Ie)
    Figure 2017538677
    (Ie1)
    Figure 2017538677
    (If)
    Figure 2017538677
    (Ig)
    Figure 2017538677
    (Ih)
    Figure 2017538677
    (Ii)
    または
    Figure 2017538677
    (Ij)
    で示される請求項1に記載の化合物。
  3. 実施例で提供される化合物。
  4. 請求項1に記載の化合物および医薬的に許容される賦形剤を含む、医薬組成物。
  5. 請求項1に記載の化合物を含む、IDOにより少なくとも一部介在される疾患、障害または病気の治療剤。
  6. 前記疾患、障害または病気が、癌であり、適宜、前記癌が、前立腺、結腸、直腸、膵臓、頚部、胃、子宮内膜、脳、肝臓、膀胱、卵巣、精巣、頭部、頸部、皮膚(メラノーマおよび基底細胞癌を含む)、中皮層、白血球(リンパ腫および白血病を含む)、食道、乳房、筋肉、結合組織、肺(小細胞肺癌および非小細胞癌を含む)、副腎、甲状腺、腎臓、または骨の癌;あるいは神経膠芽腫、中皮腫、腎細胞癌、胃癌、肉腫(カポジ肉腫を含む)、絨毛癌、皮膚基底細胞癌、または精上皮腫であってもよく、あるいは適宜、前記癌が、メラノーマ、大腸癌、膵臓癌、乳癌、前立腺癌、肺癌、白血病、脳腫瘍、リンパ腫、卵巣癌、およびカポジ肉腫からなる群から選択される、請求項5に記載の治療剤。
  7. 請求項1に記載の化合物および少なくとも1つのさらなる治療剤を含む組み合わせ医薬。
  8. 前記少なくとも1つのさらなる治療剤が、化学療法剤、免疫および/または炎症調節薬、抗高コレステロール血症薬、または抗感染症薬である、請求項7に記載の組み合わせ医薬。
  9. 前記少なくとも1つのさらなる治療剤が、免疫チェックポイント阻害剤である、請求項7に記載の組み合わせ医薬。
  10. 請求項1に記載の化合物および免疫チェックポイント阻害剤を含む、対象における癌の治療剤。
  11. 前記免疫チェックポイント阻害剤が、イピリムマブ、ニボルマブおよびペムブロリズマブからなる群から選択される、請求項9に記載の組み合わせ医薬または請求項10に記載の治療剤。
JP2017524423A 2014-11-05 2015-11-05 免疫調節剤 Active JP6762299B2 (ja)

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AU (1) AU2015342944A1 (ja)
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CA (1) CA2964297A1 (ja)
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Families Citing this family (72)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB201311888D0 (en) 2013-07-03 2013-08-14 Glaxosmithkline Ip Dev Ltd Novel compounds
GB201311891D0 (en) 2013-07-03 2013-08-14 Glaxosmithkline Ip Dev Ltd Novel compound
BR112016028255A2 (pt) 2014-06-06 2017-08-22 Flexus Biosciences Inc agentes imunorreguladores
EP3215141A4 (en) 2014-11-05 2018-06-06 Flexus Biosciences, Inc. Immunoregulatory agents
AR102537A1 (es) 2014-11-05 2017-03-08 Flexus Biosciences Inc Agentes inmunomoduladores
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
KR20180080189A (ko) 2015-09-01 2018-07-11 퍼스트 웨이브 바이오, 인코포레이티드 이상 염증 반응과 연관된 질환을 치료하기 위한 방법 및 조성물
CN109415320A (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
US10633342B2 (en) 2016-05-04 2020-04-28 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
KR20190003685A (ko) 2016-05-04 2019-01-09 브리스톨-마이어스 스큅 컴퍼니 인돌아민 2,3-디옥시게나제의 억제제 및 그의 사용 방법
KR20190004742A (ko) 2016-05-04 2019-01-14 브리스톨-마이어스 스큅 컴퍼니 인돌아민 2,3-디옥시게나제의 억제제 및 그의 사용 방법
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
JOP20170131B1 (ar) * 2016-06-10 2021-08-17 Lilly Co Eli مركبات 1-تيترا هيدروبيرانييل كاربونيل -2،3-ديهيدرو -1 h- اندول لعلاج السرطان
CN107674013B (zh) * 2016-08-02 2022-05-24 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
AU2017315572B2 (en) 2016-08-23 2021-07-15 Beijing Innocare Pharma Tech Co., Ltd. Fused heterocyclic derivative, preparation method therefor and medical use thereof
EP3503916A1 (en) * 2016-08-26 2019-07-03 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
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
EP3515486A4 (en) * 2016-09-26 2020-05-20 Advantagene, Inc. METHODS OF TREATING TIM-3 LEVEL INCREASE
RS61996B1 (sr) 2016-12-22 2021-07-30 Calithera Biosciences Inc Kompozicije i postupci za inhibiranje aktivnosti arginaze
WO2018136437A2 (en) * 2017-01-17 2018-07-26 Tesaro, Inc. Compounds useful as inhibitors of indoleamine 2,3-dioxygenase and/or tryptophan dioxygenase
WO2018209049A1 (en) 2017-05-12 2018-11-15 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
BR112019027259A2 (pt) * 2017-06-30 2020-07-14 Bristol-Myers Squibb Company formas amorfas e cristalinas de inibidores da ido
EP3645008A4 (en) * 2017-06-30 2020-12-09 Bristol-Myers Squibb Company SUBSTITUTED QUINOLINYCYCLOHEXYLPROPANAMIDE COMPOUNDS AND IMPROVED METHODS FOR THEIR PRODUCTION
EP3686196B1 (en) * 2017-09-20 2024-06-12 Hangzhou Innogate Pharma Co., Ltd. Polycyclic compound acting as ido inhibitor and/or ido-hdac dual inhibitor
EP3691643A4 (en) * 2017-09-29 2021-06-16 Bristol-Myers Squibb Company CANCER COMPOSITIONS AND TREATMENT METHODS
US11649212B2 (en) 2017-10-09 2023-05-16 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
WO2019074747A1 (en) * 2017-10-09 2019-04-18 Merck Sharp & Dohme Corp. NOVEL SUBSTITUTED CYCLOBUTYLBENZENE COMPOUNDS AS INHIBITORS OF INDOLEAMINE 2,3-DIOXYGENASE (IDO)
US11203592B2 (en) 2017-10-09 2021-12-21 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
EP3694503B1 (en) 2017-10-09 2023-08-02 Merck Sharp & Dohme LLC Novel substituted cyclobutylpyridine and cyclobutylpyrimidine compounds as indoleamine 2,3-dioxygenase (ido) inhibitors
WO2019078968A2 (en) 2017-10-18 2019-04-25 Angex Pharmaceutical, Inc. CYCLIC COMPOUNDS AS IMMUNOMODULATORS
US10800757B2 (en) 2017-10-27 2020-10-13 Boehringer Ingelheim International Gmbh Inhibitors of TRPC6
BR112020010964A2 (pt) * 2017-12-05 2020-11-17 Glaxosmithkline Intellectual Property Development Limited moduladores da indolamina 2,3-dioxigenase
CN109928921A (zh) * 2017-12-18 2019-06-25 成都华健未来科技有限公司 Ido抑制剂
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
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
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
MX2020007066A (es) 2018-01-05 2020-09-09 Dicerna Pharmaceuticals Inc Reduccion de la expresion de beta-catenina e ido para potenciar la inmunoterapia.
US11447449B2 (en) 2018-01-05 2022-09-20 Bristol-Myers Squibb Company Inhibitors of indoleamine 2,3-dioxygenase and methods of their use
BR112020014169A2 (pt) * 2018-01-10 2020-12-08 Recurium Ip Holdings, Llc Compostos de benzamida
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
EP4227302A1 (en) 2018-02-13 2023-08-16 Gilead Sciences, Inc. Pd-1/pd-l1 inhibitors
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
WO2019168866A1 (en) * 2018-02-28 2019-09-06 Dart Neuroscience, Llc Substituted cyclohexyl compounds as nop inhibitors
WO2019170543A1 (en) 2018-03-07 2019-09-12 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
CN112041311B (zh) 2018-04-19 2023-10-03 吉利德科学公司 Pd-1/pd-l1抑制剂
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
CN112384505A (zh) * 2018-07-06 2021-02-19 吉利德科学公司 治疗性的杂环化合物
TWI809427B (zh) 2018-07-13 2023-07-21 美商基利科學股份有限公司 Pd‐1/pd‐l1抑制劑
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
US20210355113A1 (en) 2018-07-23 2021-11-18 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
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
EP3870566A1 (en) 2018-10-24 2021-09-01 Gilead Sciences, Inc. Pd-1/pd-l1 inhibitors
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
AU2021324376A1 (en) 2020-08-13 2023-02-02 Boehringer Ingelheim International Gmbh Treatment of cognitive impairement associated with schizophrenia
EP4052705A1 (en) 2021-03-05 2022-09-07 Universität Basel Vizerektorat Forschung Compositions for the treatment of ebv associated diseases or conditions
BR112023017582A2 (pt) 2021-03-05 2023-12-05 Univ Basel Composições para o tratamento de doenças ou condições associadas ao ebv
WO2022261404A1 (en) * 2021-06-11 2022-12-15 Neuronascent, Inc. Methods and compositions for lipid formulation of lipophilic small molecule therapies of the heterocyclic type

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
AU1628599A (en) 1997-12-05 1999-06-28 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
US6686376B2 (en) * 2000-06-23 2004-02-03 Eli Lilly And Company Methods and compounds for inhibiting MRP1
EP1317425B1 (en) * 2000-09-11 2004-11-03 Pfizer Products Inc. Resorcinol derivatives
CA2423262A1 (en) * 2000-09-21 2002-03-28 Pfizer Products Inc. Resorcinol derivatives
EP1217000A1 (en) * 2000-12-23 2002-06-26 Aventis Pharma Deutschland GmbH Inhibitors of factor Xa and factor VIIa
US7816363B2 (en) * 2002-03-13 2010-10-19 Janssen Pharmaceutica, N.V. Inhibitors of histone deacetylase
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
US7244727B2 (en) * 2002-11-22 2007-07-17 Japan Tobacco Inc. Fused bicyclic nitrogen-containing heterocycles
WO2004054974A2 (en) 2002-12-13 2004-07-01 Smithkline Beecham Corporation Piperidine derivatives as ccr5 antagonists
AU2004215428B2 (en) * 2003-02-26 2009-08-27 Sugen LLC Aminoheteroaryl compounds as protein kinase inhibitors
JP2006521377A (ja) 2003-03-27 2006-09-21 ランケナー インスティテュート フォー メディカル リサーチ 新型ido阻害剤とその使用方法
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
EP1684762A4 (en) * 2003-11-13 2009-06-17 Ambit Biosciences Corp UREA DERIVATIVES AS MODULATORS OF KINASE
BRPI0507636A (pt) 2004-02-11 2007-07-10 Pfizer compostos, derivados terapêuticos de amida, composição farmacêutica, uso dos mesmos e combinação
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
PT2343320T (pt) 2005-03-25 2018-01-23 Gitr Inc Anticorpos anti-gitr e as suas utilizações
CN101203483A (zh) * 2005-04-21 2008-06-18 大日本住友制药株式会社 N-取代的苯乙酰胺衍生物和包含该衍生物的药物组合物
MY153424A (en) 2005-05-10 2015-02-13 Incyte Corp Modulators of indoleamine 2,3-dioxygenase and methods of using the same
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
RS54271B1 (en) 2005-07-01 2016-02-29 E. R. Squibb & Sons, L.L.C. HUMAN MONOCLONIC ANTIBODIES FOR LIGAND PROGRAMMED DEATH 1 (PD-L1)
MY148491A (en) * 2005-11-17 2013-04-30 Osi Pharm Inc FUSED BICYCLIC mTOR INHIBITORS
WO2007082079A2 (en) * 2006-01-12 2007-07-19 The Scripps Research Institute Piperidine amide derivatives as protein kinase inhibitors
WO2007095050A2 (en) * 2006-02-09 2007-08-23 Incyte Corporation N-hydroxyguanidines as modulators of indoleamine 2,3-dioxygenase
EP1996193A2 (en) * 2006-03-13 2008-12-03 OSI Pharmaceuticals, Inc. Combined treatment with an egfr kinase inhibitor and an agent that sensitizes tumor cells to the effects of egfr kinase inhibitors
US20080039453A1 (en) 2006-03-20 2008-02-14 David Putman Enantiomerically pure R-etifoxine, pharmaceutical compositions thereof and methods of their use
US20080064717A1 (en) * 2006-05-19 2008-03-13 Rajesh Iyengar Inhibitors of diacylglycerol O-acyltransferase type 1 enzyme
UA107583C2 (ru) 2006-06-01 2015-01-26 Санофі-Авентіс Спироциклические нитрилы как ингибиторы протеазы
US20080119491A1 (en) 2006-09-19 2008-05-22 Incyte Corporation Amidinoheterocycles as modulators of indoleamine 2,3-dioxygenase
CA2668579A1 (en) 2006-11-06 2008-06-05 Neurogen Corporation Cis-cyclohexyl substituted pyrimidinone derivatives
JP2010513458A (ja) 2006-12-19 2010-04-30 ファイザー・プロダクツ・インク H−pgdsの阻害剤としてのニコチンアミド誘導体、およびプロスタグランジンd2の仲介による疾患を治療するためのその使用
CA2673586A1 (en) * 2006-12-26 2008-07-24 Amgen Inc. N-cyclohexyl benzamides and benzeneacetamides as inhibitors of 11-beta-hydroxysteroid dehydrogenases
BRPI0721180A2 (pt) * 2006-12-27 2014-03-18 Sanofi Aventis Derivados de isoquinolina substituídos com cicloalquilamina
JP2010527915A (ja) * 2007-04-26 2010-08-19 アバロン ファーマシューティカルズ,インコーポレイテッド 多重環化合物及びその用途
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
EP2170059B1 (en) * 2007-06-20 2014-11-19 Merck Sharp & Dohme Corp. Cetp inhibitors derived from benzoxazole arylamides
US20090023773A1 (en) * 2007-06-27 2009-01-22 Painceptor Pharma Corporation Compositions and methods for modulating gated ion channels
WO2009008992A2 (en) * 2007-07-06 2009-01-15 Osi Pharmaceuticals Inc. Combination anti-cancer therapy comprising an inhibitor of both mtorc1 and mt0rc2
CA2693677C (en) 2007-07-12 2018-02-13 Tolerx, 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
WO2009052320A1 (en) * 2007-10-16 2009-04-23 Northeastern University Methods and compounds for modulating cannabinoid activity
ES2525244T3 (es) * 2008-03-18 2014-12-19 Arena Pharmaceuticals, Inc. Moduladores del receptor de prostaciclina (PGI2) útiles para el tratamiento de trastornos relacionados con el mismo
BR122013017387A2 (pt) 2008-03-27 2019-10-15 Grünenthal GmbH Compostos derivados substituídos de 4-aminociclohexano, composição farmacêutica e uso dos referidos compostos
WO2009151800A1 (en) * 2008-05-07 2009-12-17 Merck & Co., Inc. Soluble epoxide hydrolase inhibitors, compositions containing such compounds and methods of treatment
NZ590268A (en) 2008-07-08 2012-11-30 Incyte Corp 1,2,5-oxadiazoles as inhibitors of indoleamine 2,3-dioxygenase
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
EP4169951A1 (en) 2008-12-09 2023-04-26 F. Hoffmann-La Roche AG Anti-pd-l1 antibodies and their use to enhance t-cell function
SG172352A1 (en) 2008-12-23 2011-07-28 Abbott Lab Anti-viral compounds
AU2010215041A1 (en) * 2009-02-23 2011-07-28 Merck Canada Inc. Heterocyclic derivatives as inhibitors of stearoyl-coenzyme A delta-9 desaturase
CA2772613C (en) 2009-09-03 2020-03-10 Schering Corporation Anti-gitr antibodies
HUE026201T2 (en) 2009-12-10 2016-05-30 Hoffmann La Roche Antibodies that bind to human CSF1R extracellular domain 4 and their use
CN106279416B (zh) 2010-03-04 2019-08-30 宏观基因有限公司 与b7-h3反应性的抗体、其免疫学活性片段及其用途
CA2789071C (en) 2010-03-05 2018-03-27 F. Hoffmann-La Roche Ag Antibodies against human csf-1r and uses thereof
RU2617971C2 (ru) 2010-03-05 2017-04-28 Ф.Хоффманн-Ля Рош Аг Антитела против csf-1r человека и их применение
BR112012027308B1 (pt) 2010-04-24 2021-07-06 Mycovia Pharmaceuticals, Inc. compostos inibidores de metaloenzima e composições compreendendo os mesmos
CN106977603B (zh) 2010-05-04 2020-11-27 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
SG10201912092VA (en) 2010-09-09 2020-02-27 Pfizer 4-1bb binding molecules
US9446763B2 (en) 2010-12-23 2016-09-20 Magna Powertrain Inc. Controlled gerotor actuated pre-trans parallel hybrid
KR101970025B1 (ko) 2011-04-20 2019-04-17 메디뮨 엘엘씨 B7-h1 및 pd-1과 결합하는 항체 및 다른 분자들
WO2012158784A2 (en) * 2011-05-16 2012-11-22 Theodore Mark Kamenecka Modulators of the nuclear hormone receptor ror
AU2012311698B2 (en) * 2011-09-22 2017-06-22 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
DK2785375T3 (da) 2011-11-28 2020-10-12 Merck Patent Gmbh Anti-pd-l1-antistoffer og anvendelser deraf
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
KR20140127855A (ko) 2012-02-06 2014-11-04 제넨테크, 인크. Csf1r 억제제를 사용하는 조성물 및 방법
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
KR20150018533A (ko) 2012-05-11 2015-02-23 파이브 프라임 테라퓨틱스, 인크. 콜로니 자극 인자 1 수용체(csf1r)에 결속하는 항체들에 의한 질병 상태의 치료 방법
EA028063B1 (ru) * 2012-06-26 2017-10-31 Байер Фарма Акциенгезельшафт N-[4-(хинолин-4-илокси)циклогексил(метил)](гетеро)арилкарбоксамиды в качестве антагонистов андрогенного рецептора, их получение и применение в качестве лекарственных средств
AR091649A1 (es) 2012-07-02 2015-02-18 Bristol Myers Squibb Co Optimizacion de anticuerpos que se fijan al gen de activacion de linfocitos 3 (lag-3) y sus usos
WO2014007998A1 (en) * 2012-07-06 2014-01-09 The Regents Of The University Of California SORAFENIB DERIVATIVES AS p21 INHIBITORS
WO2014036412A2 (en) 2012-08-30 2014-03-06 Amgen Inc. A method for treating melanoma using a herpes simplex virus and an immune checkpoint inhibitor
CN104684582A (zh) 2012-08-31 2015-06-03 戊瑞治疗有限公司 用结合群落刺激因子1受体(csf1r)的抗体治疗病状的方法
SG11201506918WA (en) 2013-03-15 2015-09-29 Bristol Myers Squibb Co Inhibitors of indoleamine 2,3-dioxygenase (ido)
US20160045556A1 (en) 2013-03-29 2016-02-18 Biomed Valley Discoveries, Inc. C. novyi for the treatment of solid tumors in non-human animals
BR112016028255A2 (pt) 2014-06-06 2017-08-22 Flexus Biosciences Inc agentes imunorreguladores
GB201419579D0 (en) 2014-11-03 2014-12-17 Iomet Pharma Ltd Pharmaceutical compound
AR102537A1 (es) 2014-11-05 2017-03-08 Flexus Biosciences Inc Agentes inmunomoduladores
EP3215141A4 (en) 2014-11-05 2018-06-06 Flexus Biosciences, Inc. Immunoregulatory agents
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

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