MA53665A - Agonistes du récepteur farnésoïde x et leurs utilisations - Google Patents
Agonistes du récepteur farnésoïde x et leurs utilisationsInfo
- Publication number
- MA53665A MA53665A MA053665A MA53665A MA53665A MA 53665 A MA53665 A MA 53665A MA 053665 A MA053665 A MA 053665A MA 53665 A MA53665 A MA 53665A MA 53665 A MA53665 A MA 53665A
- Authority
- MA
- Morocco
- Prior art keywords
- farnesoid
- receptor agonists
- agonists
- receptor
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
- C07D471/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Gastroenterology & Hepatology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Virology (AREA)
- Molecular Biology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Biotechnology (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201862733004P | 2018-09-18 | 2018-09-18 | |
| US201862733006P | 2018-09-18 | 2018-09-18 | |
| US201962881560P | 2019-08-01 | 2019-08-01 | |
| PCT/US2019/051603 WO2020061113A1 (fr) | 2018-09-18 | 2019-09-17 | Agonistes du récepteur farnésoïde x et leurs utilisations |
| EP19862391.0A EP3852748B1 (fr) | 2018-09-18 | 2019-09-17 | Agonistes du récepteur farnésoïde x et leurs utilisations |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MA53665A true MA53665A (fr) | 2021-07-28 |
| MA53665B1 MA53665B1 (fr) | 2025-09-30 |
Family
ID=69887982
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA53665A MA53665B1 (fr) | 2018-09-18 | 2019-09-17 | Agonistes du récepteur farnésoïde x et leurs utilisations |
Country Status (27)
| Country | Link |
|---|---|
| US (4) | US11084817B2 (fr) |
| EP (2) | EP3852748B1 (fr) |
| JP (1) | JP7554739B2 (fr) |
| KR (2) | KR20250073553A (fr) |
| CN (1) | CN113056271B (fr) |
| AU (2) | AU2019344903B2 (fr) |
| BR (1) | BR112021004919A2 (fr) |
| CA (1) | CA3112411A1 (fr) |
| CL (1) | CL2021000632A1 (fr) |
| DK (1) | DK3852748T3 (fr) |
| ES (1) | ES3051007T3 (fr) |
| FI (1) | FI3852748T3 (fr) |
| HR (1) | HRP20251321T1 (fr) |
| IL (1) | IL281475B2 (fr) |
| LT (1) | LT3852748T (fr) |
| MA (1) | MA53665B1 (fr) |
| MD (1) | MD3852748T2 (fr) |
| MX (1) | MX2021003110A (fr) |
| PH (1) | PH12021550605A1 (fr) |
| PL (1) | PL3852748T3 (fr) |
| PT (1) | PT3852748T (fr) |
| RS (1) | RS67371B1 (fr) |
| SG (1) | SG11202102651SA (fr) |
| SI (1) | SI3852748T1 (fr) |
| SM (1) | SMT202600076T1 (fr) |
| TW (1) | TWI833805B (fr) |
| WO (1) | WO2020061113A1 (fr) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2018236275B2 (en) | 2017-03-15 | 2022-05-12 | Eli Lilly And Company | Farnesoid X receptor agonists and uses thereof |
| DK3596053T3 (da) | 2017-03-15 | 2023-09-25 | Organovo Inc | Farnesoid-x-receptoragonister og anvendelser deraf |
| EP3852748B1 (fr) | 2018-09-18 | 2025-09-03 | Eli Lilly and Company | Agonistes du récepteur farnésoïde x et leurs utilisations |
| IL293892A (en) | 2020-01-15 | 2022-08-01 | Inserm Institut National De La Sant? Et De La Rech M?Dicale | Use of fxr agonists for treating an infection by hepatitis d virus |
| CN120227340A (zh) * | 2020-03-18 | 2025-07-01 | 伊莱利利公司 | 法尼醇x受体激动剂的制剂 |
| KR20220154801A (ko) * | 2020-03-18 | 2022-11-22 | 메타크린, 인크. | 질환의 치료를 위한 파르네소이드 x 수용체 작용제 |
| JP7664278B2 (ja) * | 2020-03-18 | 2025-04-17 | オルガノボ,インク. | ファルネソイドx受容体アゴニストの結晶質形態 |
| MX2023008365A (es) | 2021-01-14 | 2023-10-04 | Enyo Pharma | Efecto sinérgico de un agonista de fxr e ifn para el tratamiento de infección por hbv. |
| TW202308629A (zh) | 2021-04-28 | 2023-03-01 | 法商Enyo製藥公司 | 使用fxr激動劑作為組合治療以增強tlr3激動劑之療效 |
| CN116554121A (zh) * | 2023-05-05 | 2023-08-08 | 济南悟通生物科技有限公司 | 一种2-异丁基噻唑的合成方法 |
Family Cites Families (68)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU4537900A (en) | 1999-05-17 | 2000-12-05 | Agouron Pharmaceuticals, Inc. | Glucagon antagonists/inverse agonists |
| EP1187810A2 (fr) | 1999-05-25 | 2002-03-20 | Sepracor, Inc. | Composes heterocycliques analgesiques et procedes d'utilisation de ces derniers |
| US6511980B2 (en) | 2000-05-05 | 2003-01-28 | Ortho Mcneil Pharmaceutical, Inc. | Substituted diamine derivatives useful as motilin antagonists |
| WO2001092226A1 (fr) | 2000-05-25 | 2001-12-06 | Sepracor, Inc. | Composes analgesiques heterocycliques et technique d'utilisation de ceux-ci |
| HUP0303360A2 (hu) | 2000-09-25 | 2004-01-28 | Actelion Pharmaceuticals Ltd. | Maláriaellenes hatású szubsztituált amino-aza-cikloalkánok és ezeket tartalmazó gyógyszerkészítmények |
| FR2815032B1 (fr) | 2000-10-10 | 2003-08-08 | Pf Medicament | Nouveaux derives d'aminophenyle piperazine ou d'amino phenyle piperide inhibiteurs de proteines prenyl transferase ainsi que leurs preparations |
| FR2825706B1 (fr) | 2001-06-06 | 2003-12-12 | Pf Medicament | Nouveaux derives de benzothienyle ou d'indole, leur preparation et leur utilisation comme inhibiteurs de proteines prenyl transferase |
| FR2839974B1 (fr) | 2002-05-24 | 2004-07-16 | Pf Medicament | Derives de phenyl-furane ou de phenyl-thiophene,leur preparation et leur application a titre de medicament |
| WO2004009549A2 (fr) | 2002-07-18 | 2004-01-29 | Actelion Pharmaceuticals Ltd | Piperidines utiles pour traiter des maladies du systeme nerveux central |
| MXPA05003054A (es) | 2002-09-20 | 2005-05-27 | Pfizer Prod Inc | Ligandos de amida y sulfonamida para el receptor de estrogenos. |
| AU2003290796A1 (en) | 2002-11-14 | 2004-06-15 | The Scripps Research Institute | Non-steroidal fxr agonists |
| WO2004046323A2 (fr) | 2002-11-15 | 2004-06-03 | The Salk Institute For Biological Studies | Structure du domaine de fixation du ligand du recepteur farnesoide x et procedes d'utilisation de celle-ci |
| US20050143449A1 (en) | 2002-11-15 | 2005-06-30 | The Salk Institute For Biological Studies | Non-steroidal farnesoid X receptor modulators and methods for the use thereof |
| GB0309781D0 (en) | 2003-04-29 | 2003-06-04 | Glaxo Group Ltd | Compounds |
| US7754711B2 (en) | 2003-07-30 | 2010-07-13 | Xenon Pharmaceuticals Inc. | Pyridazine derivatives and their use as therapeutic agents |
| EP2316827B1 (fr) | 2003-07-30 | 2016-01-27 | Xenon Pharmaceuticals Inc. | Derives de piperazine et leurs utilisations en tant qu'agents therapeutiques |
| US7759348B2 (en) | 2003-07-30 | 2010-07-20 | Xenon Pharmaceuticals Inc. | Pyridazine derivatives and their use as therapeutic agents |
| WO2005058822A1 (fr) | 2003-12-17 | 2005-06-30 | Actelion Pharmaceuticals Ltd | Cycloalcanes amines substitues |
| JP2007530582A (ja) | 2004-03-26 | 2007-11-01 | ライジェル ファーマシューティカルズ, インコーポレイテッド | 代謝可能部分を含む複素環抗ウイルス化合物およびその使用 |
| US20050272784A1 (en) | 2004-05-07 | 2005-12-08 | Xiaobing Li | Inhibitors of bacterial Type III protein secretion systems |
| JP2006199656A (ja) | 2005-01-24 | 2006-08-03 | Kowa Co | アミド基を有する環状アミン化合物 |
| MY144229A (en) | 2006-01-26 | 2011-08-15 | Xenon Pharmaceuticals Inc | Pyridazine derivatives and their use as therapeutic agents |
| CA2644369A1 (fr) | 2006-03-28 | 2007-10-04 | Novartis Ag | Amides heterocycliques destines a une utilisation en tant que produits pharmaceutiques |
| US20080081824A1 (en) | 2006-09-29 | 2008-04-03 | Bristol-Myers Squibb Company | Substituted piperidines as modulators of chemokine receptor activity |
| WO2008065500A2 (fr) | 2006-11-30 | 2008-06-05 | Pfizer Products Inc. | Hétéroaryl amides comme inhibiteurs du transport de la glycine de type i |
| EP2234977A4 (fr) | 2007-12-19 | 2011-04-13 | Boehringer Ingelheim Int | Inhibiteurs de polymérase virale |
| WO2010001869A1 (fr) | 2008-06-30 | 2010-01-07 | 武田薬品工業株式会社 | Composé de benzène tétrasubstitué et son utilisation |
| JP2010077109A (ja) | 2008-08-28 | 2010-04-08 | Takeda Chem Ind Ltd | 複素環化合物およびその用途 |
| US8435980B2 (en) | 2009-07-15 | 2013-05-07 | Abbvie Inc. | Pyrrolopyridine inhibitors of kinases |
| AU2010272523A1 (en) | 2009-07-15 | 2012-02-02 | Merck Serono S.A. | Tetrazole derivatives |
| FR2963005B1 (fr) | 2010-07-23 | 2012-08-17 | Sanofi Aventis | Derives d'oxadiazoles et de pyridazines, leur preparation et leur application en therapeutique |
| ME02754B (fr) | 2011-03-23 | 2018-01-20 | Trevena Inc | Ligands de récepteurs opïoides, et leurs procédés d'utilisation et de production |
| WO2013008706A1 (fr) | 2011-07-13 | 2013-01-17 | エム・テクニック株式会社 | Procédé de fabrication de microparticules avec diamètre de cristallites régulé |
| EP2545964A1 (fr) | 2011-07-13 | 2013-01-16 | Phenex Pharmaceuticals AG | Nouveaux composés se liant au fxr (nr1 h4) et modulant son activité |
| RU2543485C2 (ru) | 2013-02-26 | 2015-03-10 | Андрей Александрович Иващенко | Гетероциклические агонисты рецепторов желчных кислот tgr5, фармацевтическая композиция, способы их получения и применения |
| GB201316824D0 (en) | 2013-09-23 | 2013-11-06 | R & D Vernalis Ltd | New Chemical Entities |
| JP2017511304A (ja) | 2014-03-13 | 2017-04-20 | ソーク インスティチュート フォー バイオロジカル スタディーズ | フェキサラミン類似体ならびに作製方法および使用方法 |
| CA2942403A1 (fr) | 2014-03-13 | 2015-09-17 | Salk Institute For Biological Studies | Agonistes fxr et leurs procedes de fabrication et d'utilisation |
| US10077268B2 (en) | 2014-03-13 | 2018-09-18 | Salk Institute For Biological Studies | FXR agonists and methods for making and using |
| US20150258052A1 (en) | 2014-03-13 | 2015-09-17 | Salk Institute For Biological Studies | Methods of using fexaramine and agents that increase sympathetic nervous system activity to promote browning of white adipose tissue |
| US10301268B2 (en) | 2014-03-13 | 2019-05-28 | The Salk Institute For Biological Studies | Analogs of fexaramine and methods of making and using |
| US20180116993A1 (en) | 2015-01-22 | 2018-05-03 | Xiamen University | Modulators of farnesoid x receptor and methods for the use thereof |
| AU2016233579A1 (en) | 2015-03-13 | 2017-10-12 | Salk Institute For Biological Studies | Treating latent autoimmune diabetes of adults with farnesoid X receptor agonists to activate intestinal receptors |
| WO2017018751A1 (fr) | 2015-07-24 | 2017-02-02 | 동국대학교 산학협력단 | Nouveau composé présentant une activité inhibitrice de blt et composition, destiné à prévenir ou à traiter des maladies inflammatoires, contenant ce dernier en tant que principe actif |
| EP3350166A4 (fr) * | 2015-09-16 | 2019-05-01 | Metacrine, Inc. | Agonistes du récepteur x farnésoïde et leurs utilisations |
| EP3350165B1 (fr) | 2015-09-16 | 2023-07-26 | Organovo, Inc. | Agonistes du récepteur x farnésoïde et leurs utilisations |
| WO2017049176A1 (fr) * | 2015-09-16 | 2017-03-23 | Metacrine, Inc. | Agonistes du récepteur x farnésoïde et leurs utilisations |
| US10626081B2 (en) | 2015-09-16 | 2020-04-21 | Metacrine, Inc. | Farnesoid X receptor agonists and uses thereof |
| CN105477636B (zh) * | 2015-10-16 | 2019-09-17 | 厦门大学 | 使用阿维菌素及其衍生物治疗代谢疾病的方法 |
| CN107126419B (zh) | 2016-02-26 | 2020-06-19 | 石药集团中诺药业(石家庄)有限公司 | 一种奥贝胆酸片剂及其制备方法 |
| KR102316645B1 (ko) | 2016-03-31 | 2021-10-25 | 가부시키가이샤 아데카 | 감광성 조성물 및 신규 화합물 |
| WO2018170173A1 (fr) * | 2017-03-15 | 2018-09-20 | Metacrine, Inc. | Agonistes du récepteur farnésoïde x et leurs utilisations |
| DK3596053T3 (da) | 2017-03-15 | 2023-09-25 | Organovo Inc | Farnesoid-x-receptoragonister og anvendelser deraf |
| AU2018236275B2 (en) | 2017-03-15 | 2022-05-12 | Eli Lilly And Company | Farnesoid X receptor agonists and uses thereof |
| US20200131132A1 (en) | 2017-03-15 | 2020-04-30 | Metacrine, Inc. | Farnesoid x receptor agonists and uses thereof |
| WO2018170165A1 (fr) | 2017-03-15 | 2018-09-20 | Metacrine, Inc. | Agonistes du récepteur farnésoïde x et leurs utilisations |
| CZ2017298A3 (cs) | 2017-05-26 | 2018-12-05 | Zentiva, K.S. | Amorfní formy obeticholové kyseliny |
| WO2020060007A1 (fr) | 2018-09-17 | 2020-03-26 | 엘지전자 주식회사 | Procédé et dispositif sans fil pour gérer une session de pdu dans une communication mobile 5g |
| US20220047553A1 (en) | 2018-09-18 | 2022-02-17 | Metacrine, Inc. | Farnesoid x receptor agonists for the treatment of disease |
| BR112021004931A2 (pt) | 2018-09-18 | 2021-06-01 | Metacrine, Inc. | formas cristalinas de um agonista de receptor farnesoide x |
| CN113056264A (zh) | 2018-09-18 | 2021-06-29 | 梅塔科林公司 | 法尼醇x受体激动剂及其用途 |
| WO2020061116A1 (fr) | 2018-09-18 | 2020-03-26 | Metacrine, Inc. | Agonistes du récepteur farnésoïde x et leurs utilisations |
| WO2020061117A1 (fr) | 2018-09-18 | 2020-03-26 | Metacrine, Inc. | Agonistes du récepteur farnésoïde x et leurs utilisations |
| EP3852748B1 (fr) | 2018-09-18 | 2025-09-03 | Eli Lilly and Company | Agonistes du récepteur farnésoïde x et leurs utilisations |
| WO2020061118A1 (fr) | 2018-09-18 | 2020-03-26 | Metacrine, Inc. | Agonistes du récepteur farnésoïde x et leurs utilisations |
| JP7664278B2 (ja) | 2020-03-18 | 2025-04-17 | オルガノボ,インク. | ファルネソイドx受容体アゴニストの結晶質形態 |
| CN120227340A (zh) | 2020-03-18 | 2025-07-01 | 伊莱利利公司 | 法尼醇x受体激动剂的制剂 |
| KR20220154801A (ko) | 2020-03-18 | 2022-11-22 | 메타크린, 인크. | 질환의 치료를 위한 파르네소이드 x 수용체 작용제 |
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2019
- 2019-09-17 EP EP19862391.0A patent/EP3852748B1/fr active Active
- 2019-09-17 MA MA53665A patent/MA53665B1/fr unknown
- 2019-09-17 KR KR1020257016139A patent/KR20250073553A/ko active Pending
- 2019-09-17 MX MX2021003110A patent/MX2021003110A/es unknown
- 2019-09-17 BR BR112021004919-3A patent/BR112021004919A2/pt unknown
- 2019-09-17 JP JP2021513407A patent/JP7554739B2/ja active Active
- 2019-09-17 IL IL281475A patent/IL281475B2/en unknown
- 2019-09-17 MD MDE20210696T patent/MD3852748T2/ro unknown
- 2019-09-17 RS RS20251101A patent/RS67371B1/sr unknown
- 2019-09-17 PT PT198623910T patent/PT3852748T/pt unknown
- 2019-09-17 LT LTEPPCT/US2019/051603T patent/LT3852748T/lt unknown
- 2019-09-17 AU AU2019344903A patent/AU2019344903B2/en active Active
- 2019-09-17 DK DK19862391.0T patent/DK3852748T3/da active
- 2019-09-17 SM SM20260076T patent/SMT202600076T1/it unknown
- 2019-09-17 ES ES19862391T patent/ES3051007T3/es active Active
- 2019-09-17 US US16/573,993 patent/US11084817B2/en active Active
- 2019-09-17 FI FIEP19862391.0T patent/FI3852748T3/fi active
- 2019-09-17 EP EP25178478.1A patent/EP4596543A3/fr active Pending
- 2019-09-17 CA CA3112411A patent/CA3112411A1/fr active Pending
- 2019-09-17 SI SI201930976T patent/SI3852748T1/sl unknown
- 2019-09-17 KR KR1020217011359A patent/KR102810978B1/ko active Active
- 2019-09-17 CN CN201980075902.2A patent/CN113056271B/zh active Active
- 2019-09-17 HR HRP20251321TT patent/HRP20251321T1/hr unknown
- 2019-09-17 SG SG11202102651SA patent/SG11202102651SA/en unknown
- 2019-09-17 TW TW108133441A patent/TWI833805B/zh active
- 2019-09-17 WO PCT/US2019/051603 patent/WO2020061113A1/fr not_active Ceased
- 2019-09-17 PL PL19862391.0T patent/PL3852748T3/pl unknown
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2021
- 2021-03-16 CL CL2021000632A patent/CL2021000632A1/es unknown
- 2021-03-17 PH PH12021550605A patent/PH12021550605A1/en unknown
- 2021-06-16 US US17/349,757 patent/US11773094B2/en active Active
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2023
- 2023-07-17 US US18/353,659 patent/US20230382913A1/en not_active Abandoned
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2024
- 2024-10-31 US US18/933,587 patent/US20250289821A1/en active Pending
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2025
- 2025-05-22 AU AU2025203804A patent/AU2025203804A1/en active Pending
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