JP2017510572A5 - - Google Patents

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Publication number
JP2017510572A5
JP2017510572A5 JP2016556962A JP2016556962A JP2017510572A5 JP 2017510572 A5 JP2017510572 A5 JP 2017510572A5 JP 2016556962 A JP2016556962 A JP 2016556962A JP 2016556962 A JP2016556962 A JP 2016556962A JP 2017510572 A5 JP2017510572 A5 JP 2017510572A5
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JP
Japan
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compound
aliphatic
present
alkyl
subject
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JP2016556962A
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English (en)
Japanese (ja)
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JP2017510572A (ja
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Priority claimed from PCT/US2015/020582 external-priority patent/WO2015138986A1/en
Publication of JP2017510572A publication Critical patent/JP2017510572A/ja
Publication of JP2017510572A5 publication Critical patent/JP2017510572A5/ja
Pending legal-status Critical Current

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JP2016556962A 2014-03-13 2015-03-13 Fxrアゴニストならびに作製および使用のための方法 Pending JP2017510572A (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201461952754P 2014-03-13 2014-03-13
US61/952,754 2014-03-13
US201462061463P 2014-10-08 2014-10-08
US62/061,463 2014-10-08
PCT/US2015/020582 WO2015138986A1 (en) 2014-03-13 2015-03-13 Fxr agonists and methods for making and using

Publications (2)

Publication Number Publication Date
JP2017510572A JP2017510572A (ja) 2017-04-13
JP2017510572A5 true JP2017510572A5 (enExample) 2017-06-29

Family

ID=54072502

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2016556962A Pending JP2017510572A (ja) 2014-03-13 2015-03-13 Fxrアゴニストならびに作製および使用のための方法

Country Status (6)

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EP (1) EP3116878A4 (enExample)
JP (1) JP2017510572A (enExample)
KR (1) KR20160132111A (enExample)
AU (1) AU2015229072A1 (enExample)
CA (1) CA2942403A1 (enExample)
WO (1) WO2015138986A1 (enExample)

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2545964A1 (en) 2011-07-13 2013-01-16 Phenex Pharmaceuticals AG Novel FXR (NR1H4) binding and activity modulating compounds
US10301268B2 (en) 2014-03-13 2019-05-28 The Salk Institute For Biological Studies Analogs of fexaramine and methods of making and using
US10077268B2 (en) 2014-03-13 2018-09-18 Salk Institute For Biological Studies FXR agonists and methods for making and using
WO2016014927A2 (en) 2014-07-24 2016-01-28 W.R. Grace & Co.-Conn. Crystalline form of nicotinamide riboside
TWI698430B (zh) 2015-02-13 2020-07-11 南北兄弟藥業投資有限公司 三環化合物及其在藥物中的應用
KR102629310B1 (ko) 2015-03-09 2024-01-24 더블유.알. 그레이스 앤드 캄파니-콘. 니코틴아미드 리보사이드의 결정 형태
KR20180052678A (ko) 2015-09-16 2018-05-18 메타크린, 인크. 파네소이드 x 수용체 아고니스트 및 이의 용도
WO2017078928A1 (en) * 2015-11-06 2017-05-11 Salk Institute For Biological Studies Fxr agonists and methods for making and using
WO2017143134A1 (en) * 2016-02-19 2017-08-24 Alios Biopharma, Inc. Fxr modulators and methods of their use
BR112018075734A2 (pt) * 2016-06-13 2019-04-02 Gilead Sciences, Inc. composto, composição farmacêutica, método para tratar um paciente com uma doença ou condição mediada pelo menos em parte por fxr, e, uso de um composto.
CA3252823A1 (en) * 2016-06-13 2025-02-25 Gilead Sciences, Inc. Substituted tert-butyl-3-(2-chloro-phenyl)-3-hydroxyazetidine-1-carboxylate compounds
KR102218498B1 (ko) * 2016-09-14 2021-02-22 노파르티스 아게 Fxr 작용제들의 조합물
AU2018223146B2 (en) 2017-02-21 2023-12-21 Genfit Combination of a PPAR agonist with a FXR agonist
CN110461328A (zh) 2017-03-28 2019-11-15 吉利德科学公司 治疗肝疾病的治疗组合
HRP20251321T1 (hr) 2018-09-18 2025-12-05 Eli Lilly And Company Agonisti farnezoid x receptora i njihova primjena
EP4360632B1 (en) 2019-01-15 2025-10-29 Gilead Sciences, Inc. Fxr (nr1h4) modulating compounds
US11524005B2 (en) 2019-02-19 2022-12-13 Gilead Sciences, Inc. Solid forms of FXR agonists
AU2020312735A1 (en) 2019-07-18 2021-12-16 Enyo Pharma Method for decreasing adverse-effects of interferon
CN114080234A (zh) 2019-07-23 2022-02-22 诺华股份有限公司 包含fxr激动剂的治疗
EP4003349A1 (en) 2019-07-23 2022-06-01 Novartis AG Combination treatment of liver diseases using fxr agonists
CA3153062A1 (en) 2019-09-03 2021-03-11 Novartis Ag Treatment of liver disease or disorder comprising actrii receptor antagonists
WO2021053618A1 (en) 2019-09-19 2021-03-25 Novartis Ag Treatment comprising fxr agonists
EP4041233A1 (en) 2019-09-30 2022-08-17 Novartis AG Treatment comprising the use of fxr agonists
TW202135811A (zh) 2019-12-20 2021-10-01 瑞士商諾華公司 使用整聯蛋白抑制劑組合治療肝臟疾病
US20230060715A1 (en) 2020-01-15 2023-03-02 INSERM (Institut National de la Santé et de la Recherche Médicale) Use of fxr agonists for treating an infection by hepatitis d virus
BR112022018553A2 (pt) 2020-03-18 2022-11-29 Metacrine Inc Formulações de um agonista do receptor x farnesoide
MX2022011582A (es) 2020-03-18 2022-12-13 Metacrine Inc Formas cristalinas de un agonista del receptor farnesoide x.
WO2022101853A1 (en) 2020-11-16 2022-05-19 Novartis Ag Method of determining liver fibrosis
US20240100125A1 (en) 2021-01-14 2024-03-28 Enyo Pharma Synergistic effect of a fxr agonist and ifn for the treatment of hbv infection
CN117320722A (zh) 2021-04-28 2023-12-29 埃尼奥制药公司 使用fxr激动剂作为联合治疗强烈增强tlr3激动剂的作用
CN120698876A (zh) * 2025-06-03 2025-09-26 上海埃思凯特科技有限公司 一种吉非罗齐氘代衍生物及其制备方法和应用

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Publication number Priority date Publication date Assignee Title
TWI329111B (en) * 2002-05-24 2010-08-21 X Ceptor Therapeutics Inc Azepinoindole and pyridoindole derivatives as pharmaceutical agents
CA2633243C (en) * 2005-12-15 2014-05-27 Exelixis, Inc. Azepinoindole derivatives as pharmaceutical agents
US20080300235A1 (en) * 2007-06-01 2008-12-04 Wyeth FXR Agonists for Reducing LOX-1 Expression
US20090163474A1 (en) * 2007-10-19 2009-06-25 Wyeth FXR Agonists for the Treatment of Nonalcoholic Fatty Liver and Cholesterol Gallstone Diseases
US20090215748A1 (en) * 2007-12-20 2009-08-27 Wyeth FXR agonists for treating vitamin D associated diseases
WO2010036362A1 (en) * 2008-09-26 2010-04-01 Wyeth 1,2,3,6-tetrahydroazepino[4,5-b]indole-5-carboxylate nuclear receptor inhibitors
EP3593802A3 (en) * 2010-05-26 2020-03-25 Satiogen Pharmaceuticals, Inc. Bile acid recycling inhibitors and satiogens for treatment of diabetes, obesity, and inflammatory gastrointestinal conditions
CA2842707A1 (en) * 2011-08-04 2013-02-07 Lumena Pharmaceuticals, Inc. Bile acid recycling inhibitors for treatment of pancreatitis

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