AR103624A1 - Composiciones farmacéuticas para terapia de combinación - Google Patents

Composiciones farmacéuticas para terapia de combinación

Info

Publication number
AR103624A1
AR103624A1 ARP160100332A ARP160100332A AR103624A1 AR 103624 A1 AR103624 A1 AR 103624A1 AR P160100332 A ARP160100332 A AR P160100332A AR P160100332 A ARP160100332 A AR P160100332A AR 103624 A1 AR103624 A1 AR 103624A1
Authority
AR
Argentina
Prior art keywords
phenyl
methyl
ppar
pharmaceutical composition
agonist
Prior art date
Application number
ARP160100332A
Other languages
English (en)
Inventor
Adorini Luciano
Pruzanski Mark
Original Assignee
Intercept Pharmaceuticals Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=56564878&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR103624(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Intercept Pharmaceuticals Inc filed Critical Intercept Pharmaceuticals Inc
Publication of AR103624A1 publication Critical patent/AR103624A1/es

Links

Classifications

    • 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
    • A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
    • A61K31/575—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of three or more carbon atoms, e.g. cholane, cholestane, ergosterol, sitosterol
    • 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
    • A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19—Carboxylic acids, e.g. valproic acid
    • A61K31/192—Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid 
    • 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
    • A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
    • A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
    • A61K31/216—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acids having aromatic rings, e.g. benactizyne, clofibrate
    • 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
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/365—Lactones
    • A61K31/366—Lactones having six-membered rings, e.g. delta-lactones
    • 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
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • 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
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/451—Non condensed piperidines, e.g. piperocaine having a carbocyclic group directly attached to the heterocyclic ring, e.g. glutethimide, meperidine, loperamide, phencyclidine, piminodine
    • 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
    • A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • 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
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • 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
    • A61P1/12—Antidiarrhoeals
    • 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
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • 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
    • A61P3/06—Antihyperlipidemics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Emergency Medicine (AREA)
  • Virology (AREA)
  • Urology & Nephrology (AREA)
  • Molecular Biology (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Vascular Medicine (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

Reivindicación 1: Una composición farmacéutica que comprende un agonista del FXR, al menos un agonista del PPAR-a, un agonista del PPAR-d y/o un agonista doble del PPAR-a y del PPAR-d y opcionalmente uno o más vehículos farmacéuticamente aceptables. Reivindicación 2: La composición farmacéutica de acuerdo con la reivindicación 1, donde el al menos un agonista del PPAR-a es un fibrato. Reivindicación 3: La composición farmacéutica de acuerdo con la reivindicación 2, donde el fibrato se selecciona entre el bezafibrato, el ciprofibrato, el clofibrato, el fenofibrato, el gemfibrozil, el binifibrato, el clinofibrato, el ácido clofíbrico, el nicofibrato, el pirifibrato, el plafibride, el ronifibrato, el teofibrato, el tocofibrato, las sales farmacéuticamente aceptables de cualquiera de éstos, los ésteres farmacéuticamente aceptables de cualquiera de éstos y los derivados del ácido 2-fenoxi-2-metilpropanoico en los cuales la unidad de fenoxilo ha sido sustituida con una piperidina, una 4-hidroxipiperidina, unas piperazina o un piperid-3-eno opcionalmente sustituido. Reivindicación 7: La composición farmacéutica de acuerdo con la reivindicación 1, donde el al menos un agonista del PPAR-d es el ácido {4-[({4-metil-2-[4-(trifluorometil)fenil]-1,3-tiazol-5-il}metil)sulfanil]-2-metilfenoxi}acético, el ácido {2-metil-4-[5-metil-2-(4-trifluorometil-fenil)-2H-[1,2,3]triazol-4-ilmetilsilfanil]-fenoxi}-acético, el ácido [4-[[[2-[3-fluoro-4-(trifluorometil)fenil]-4-metil-5-tiazolil]metil]tio]-2-metilfenoxi]-acético o una sal farmacéuticamente aceptable de cualquiera de éstos. Reivindicación 8: La composición farmacéutica de acuerdo con la reivindicación 1, donde el al menos un agonista doble del PPAR-a y del PPAR-d es el ácido 2-[2,6-dimetil-4-[3-[4-(metiltio)fenil]-3-oxo-1(E)-propenil]fenoxil]-2-metilpropanoico, el ácido (2S)-2-metoxi-3-[4-[2-(5-metil-2-fenil-4-oxazolil)etoxi]-7-benzotiofenil]propanoico, la N-[(4-metoxifenoxi)carbonil]-N-{4-[2-(5-metil-2-fenil-1,3-oxazol-4-il)etoxi]bencil}glicina, el ácido (2S)-2-etoxi-3-[4-[2-(4-metilsulfoniloxifenil)etoxi]fenil]propanoico, el ácido (2S)-2-etoxi-3-[4-(2-{2-metil-5-[4-(metilsulfanil)fenil]-1H-pirrol-1-il}etoxi)fenil]propanoico o una sal farmacéuticamente aceptable de cualquiera de éstos. Reivindicación 9: La composición farmacéutica de acuerdo con la reivindicación 1, que también comprende una estatina. Reivindicación 10: La composición farmacéutica de acuerdo con la reivindicación 9, donde la estatina se selecciona entre la simvastatina, la fluvastatina, la pravastatina, la rivastatina, la mevastatina, la atorvastatina, la cerivastatina, la lovastatina, la pitavastatina, la fluinadostatina, la velostatina, la dalvastatina, la rosuvastatina, la dihidrocompactina y la compactina. Reivindicación 12: La composición farmacéutica de acuerdo con la reivindicación 1, 9 u 11, donde el agonista del FXR es un compuesto que responde a la fórmula (1), una sal farmacéuticamente aceptable de éste o un conjugado de éste con un aminoácido, donde R¹ es hidrógeno o un alquilo C₁₋₆ no sustituido; R² es hidrógeno o a-hidroxilo; X es C(O)OH, C(O)NH(CH₂)ₘSO₃H, C(O)NH(CH₂)ₙCO₂H u OSO₃H; R⁴ es hidroxilo o hidrógeno; R⁷ es hidroxilo o hidrógeno; m es 1, 2 ó 3; y n es 1, 2 ó 3.
ARP160100332A 2015-02-06 2016-02-05 Composiciones farmacéuticas para terapia de combinación AR103624A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201562113134P 2015-02-06 2015-02-06

Publications (1)

Publication Number Publication Date
AR103624A1 true AR103624A1 (es) 2017-05-24

Family

ID=56564878

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP160100332A AR103624A1 (es) 2015-02-06 2016-02-05 Composiciones farmacéuticas para terapia de combinación

Country Status (31)

Country Link
US (3) US11311557B2 (es)
EP (2) EP4035665A1 (es)
JP (2) JP7306791B2 (es)
KR (1) KR20170115071A (es)
CN (1) CN107405325B (es)
AR (1) AR103624A1 (es)
AU (2) AU2016215179B2 (es)
BR (1) BR112017016766B1 (es)
CA (1) CA2976056C (es)
CL (3) CL2017001983A1 (es)
CO (1) CO2017007959A2 (es)
CR (1) CR20170356A (es)
DK (1) DK3253382T3 (es)
EA (1) EA036404B1 (es)
EC (1) ECSP17057848A (es)
ES (1) ES2905872T3 (es)
GT (1) GT201700174A (es)
HK (1) HK1246191A1 (es)
IL (2) IL253719B (es)
MA (1) MA40814A1 (es)
MX (1) MX2017010131A (es)
NI (1) NI201700100A (es)
PE (1) PE20180027A1 (es)
PH (1) PH12017501384A1 (es)
SG (1) SG11201706347SA (es)
SV (1) SV2017005512A (es)
TN (1) TN2017000344A1 (es)
TW (1) TW201628625A (es)
UA (1) UA125744C2 (es)
WO (1) WO2016127019A2 (es)
ZA (1) ZA201706007B (es)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2016215179B2 (en) 2015-02-06 2021-02-25 Intercept Pharmaceuticals, Inc. Pharmaceutical compositions for combination therapy
EP3280421B1 (en) 2015-04-07 2023-12-27 Intercept Pharmaceuticals, Inc. Pharmaceutical compositions for combination therapy
KR20180052756A (ko) 2015-09-24 2018-05-18 인터셉트 파마슈티컬즈, 인크. 담즙산 유도체 제조를 위한 방법 및 중간체
US11331292B2 (en) 2016-03-31 2022-05-17 Genfit Methods of treatment of cholestatic diseases
US12053445B2 (en) 2016-03-31 2024-08-06 Genfit Methods of treatment of cholestatic diseases
IL311687A (en) * 2016-03-31 2024-05-01 Genfit Methods for treating gallstone disease
BR112019011740A2 (pt) * 2016-12-09 2019-10-29 Cadila Healthcare Ltd composição farmacêutica e método para o tratamento de colangite biliar primária
MX2019009908A (es) * 2017-02-21 2019-10-14 Genfit Combinacion de un agonista de ppar con un agonista de fxr.
WO2019053582A1 (en) * 2017-09-13 2019-03-21 Novartis Ag COMBINATIONS HAVING FXR AGONISTS
GB201812382D0 (en) 2018-07-30 2018-09-12 Nzp Uk Ltd Compounds
KR20210150436A (ko) * 2019-04-10 2021-12-10 장피트 화학식 (i)의 화합물 및 glp-1 수용체 효현제를 포함하는 병용 요법
CN114144185A (zh) * 2019-05-30 2022-03-04 英特塞普特医药品公司 用于治疗胆汁淤积性肝病的包含fxr激动剂和贝特类的药物组合物
CN110287493B (zh) * 2019-06-28 2023-04-18 中国科学技术信息研究所 风险短语识别方法、装置、电子设备及存储介质
KR20220035365A (ko) * 2019-07-18 2022-03-22 엔요 파마 인터페론의 부작용을 감소시키는 방법
US20220370467A1 (en) * 2019-09-20 2022-11-24 Reneo Pharmaceuticals, Inc. Using of a ppar-delta agonist in the treatment of kidney disease
US20220387467A1 (en) * 2019-11-22 2022-12-08 Avolynt Use of sglt2 inhibitors to treat primary billiary cholangitis
CN111690731B (zh) * 2020-05-22 2021-09-28 河南大学 Fxr激动剂在治疗肝性脑病中的应用
CN112885471B (zh) * 2021-03-12 2023-01-24 上海中医药大学附属岳阳中西医结合医院 基于贝叶斯网络最大熵自学习扩展集对分析的银屑病疗效评价系统
WO2023147141A1 (en) * 2022-01-28 2023-08-03 Intercept Pharmaceuticals, Inc. Combination therapy
WO2024132001A1 (en) * 2022-12-21 2024-06-27 Charles University, Faculty Of Pharmacy In Hradec Kralove Multitarget nuclear receptor ligands based on 2-(4-(quinolin-2-yloxy)phenoxy)propanoic acid and 2-(4-(quinoxalin-2-yloxy)phenoxy)propanoic acid for the treatment of metabolic and liver diseases

Family Cites Families (65)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB860303A (en) 1958-06-20 1961-02-01 Ici Ltd Pharmaceutical compositions comprising ª‡-aryloxy-aliphatic carboxylic acids and/or ª
US3262580A (en) 1964-06-23 1966-07-26 Mcdowell Wellman Eng Co Slewable gantry crane
FR1498459A (es) 1965-07-30 1968-01-08
US3674836A (en) 1968-05-21 1972-07-04 Parke Davis & Co 2,2-dimethyl-{11 -aryloxy-alkanoic acids and salts and esters thereof
US4058552A (en) 1969-01-31 1977-11-15 Orchimed Sa Esters of p-carbonylphenoxy-isobutyric acids
FI52570C (fi) 1969-04-16 1977-10-10 Sumitomo Chemical Co Menetelmä veren kolesteroli- tai lipoidipitoisuutta alentavien fenoxia lifaattisten karboksyylihappoyhdisteiden ja -esteriyhdisteiden valmist amiseksi.
AT296986B (de) 1969-08-13 1972-03-10 Merz & Co Verfahren zur Herstellung von neuen α-Halogenphenoxy-isobutyroyl-β-nicotinoyl-glykolen
DE2230383C3 (de) 1971-10-01 1981-12-03 Boehringer Mannheim Gmbh, 6800 Mannheim Phenoxyalkylcarbonsäurederivate und Verfahren zur Herstellung derselben
JPS5118954B2 (es) 1972-02-04 1976-06-14
US3948973A (en) 1972-08-29 1976-04-06 Sterling Drug Inc. Halocyclopropyl substituted phenoxyalkanoic acids
DE2308826C3 (de) 1973-02-22 1980-03-27 Ludwig Merckle Kg Chem. Pharm. Fabrik, 7902 Blaubeuren Phenoxyalkancarbonsäureester von Oxyalkyltheophyllinen, Verfahren zu ihrer Herstellung und Arzneimittel
FR2244511B1 (es) 1973-07-05 1977-07-15 Roussel Uclaf
ES8101585A1 (es) 1980-02-15 1980-12-16 Especialidades Farmaco Terape Procedimiento de obtencion de un nuevo compuesto antiateros-clerotico
US5023252A (en) 1985-12-04 1991-06-11 Conrex Pharmaceutical Corporation Transdermal and trans-membrane delivery of drugs
ES2156120T3 (es) 1992-12-08 2001-06-16 Ss Pharmaceutical Co Derivados arilamidicos.
TWI238064B (en) 1995-06-20 2005-08-21 Takeda Chemical Industries Ltd A pharmaceutical composition for prophylaxis and treatment of diabetes
AU5928898A (en) 1997-01-24 1998-08-18 Regents Of The University Of California, The Use of fxr, pparalpha and lxralpha activators to restore barrier function, promote epidermal differentiation and inhibit proliferation
CA2296726C (en) * 1997-08-29 2004-06-29 Pfizer Products Inc. Combination therapy
PL193086B1 (pl) 1997-10-27 2007-01-31 Reddys Lab Ltd Dr Nowe związki tricykliczne i związki pośrednie, sposób ich wytwarzania, zawierające je kompozycje farmaceutyczne oraz ich zastosowanie
US20030109467A1 (en) 2001-11-15 2003-06-12 Isis Pharmaceuticals Inc. Antisense modulation of human FXR expression
EP1140036A2 (en) 1998-12-18 2001-10-10 Abbott Laboratories Novel formulations comprising lipid-regulating agents
AU2389100A (en) 1998-12-23 2000-07-12 Glaxo Group Limited Assays for ligands for nuclear receptors
WO2000040965A1 (en) 1999-01-07 2000-07-13 Tularik, Inc. Fxr receptor-mediated modulation of cholesterol metabolism
US6071955A (en) * 1999-02-25 2000-06-06 The Regents Of The University Of California FXR, PPARA and LXRA activators to treat acne/acneiform conditions
US20020132223A1 (en) 1999-03-26 2002-09-19 City Of Hope Methods for modulating activity of the FXR nuclear receptor
CA2406067A1 (en) 2000-04-19 2001-11-01 Thomas Julius Borody Compositions comprising the combination of a bile acid and a fibrate for use in therapies for hyperlipidaemia-associated disorders
US6777446B2 (en) 2000-09-05 2004-08-17 Tularik, Inc. FXR modulators
JP2004509161A (ja) 2000-09-18 2004-03-25 グラクソ　グループ　リミテッド Ｌｘｒのアゴニストとして有用な置換アミノプロポキシアリール誘導体
ES2248581T3 (es) 2001-03-12 2006-03-16 Intercept Pharmaceuticals, Inc. Esteroides como agonistas de fxr.
EP1285914B1 (en) 2001-08-13 2007-12-19 PheneX Pharmaceuticals AG Nr1h4 nuclear receptor binding compounds
US7259186B2 (en) 2002-12-17 2007-08-21 Abbott Laboratories Salts of fenofibric acid and pharmaceutical formulations thereof
EP1568706A1 (en) 2004-02-26 2005-08-31 Intercept Pharmaceuticals, Inc. Novel steroid agonist for FXR
GB0405349D0 (en) * 2004-03-10 2004-04-21 Univ Birmingham Cancer therapy and medicaments therefor
US9498484B2 (en) 2004-03-12 2016-11-22 Intercept Pharmaceuticals, Inc. Treatment of fibrosis using FXR ligands
PE20060315A1 (es) * 2004-05-24 2006-05-15 Irm Llc Compuestos de tiazol como moduladores de ppar
US20060252670A1 (en) * 2004-10-14 2006-11-09 Intercept Pharmaceuticals Inc. Method of reducing drug-induced adverse side effects in a patient
US20090131395A1 (en) 2005-05-05 2009-05-21 Microbia, Inc. Biphenylazetidinone cholesterol absorption inhibitors
ITMI20050912A1 (it) 2005-05-19 2006-11-20 Erregierre Spa Processo di preparazione di acidi 3-a-ya(b)-diidrossi-6-a(b)-alchil-5b-colanici
JP2010517931A (ja) 2006-02-14 2010-05-27 インターセプト ファーマシューティカルズ， インコーポレイテッド Ｆｘｒ媒介性の疾患または状態の予防または治療用のｆｘｒリガンドとしての胆汁酸誘導体
US20070197606A1 (en) 2006-02-22 2007-08-23 Burczynski Frank J Use of ppar agonists as anti-oxidants
CN101534641A (zh) * 2006-03-22 2009-09-16 哈佛大学校长及研究员协会 治疗高胆固醇血症和动脉粥样硬化的方法和组合物
CA2651373A1 (en) 2006-05-24 2007-12-06 Eli Lilly And Company Compounds and methods for modulating fxr
DK2029547T3 (da) 2006-05-24 2010-07-26 Lilly Co Eli FXR-agonister
JP5222846B2 (ja) 2006-06-27 2013-06-26 インターセプト ファーマシューティカルズ， インコーポレイテッド Ｆｘｒ媒介疾患または状態の予防または治療のためのｆｘｒリガンドとしての胆汁酸誘導体
WO2008015763A1 (fr) 2006-08-04 2008-02-07 Aska Pharmaceutical Co., Ltd. Formulation médicamenteuse contenant un médicament fibrate et procédé pour la produire
EP1886685A1 (en) 2006-08-11 2008-02-13 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods, uses and compositions for modulating replication of hcv through the farnesoid x receptor (fxr) activation or inhibition
EP1894928A1 (en) 2006-08-29 2008-03-05 PheneX Pharmaceuticals AG Heterocyclic fxr binding compounds
EP1894924A1 (en) 2006-08-29 2008-03-05 Phenex Pharmaceuticals AG Heterocyclic FXR binding compounds
WO2008039829A2 (en) 2006-09-26 2008-04-03 Ironwood Pharmaceuticals, Inc. Diphenylheterocycle cholesterol absorption inhibitors
CL2007003035A1 (es) * 2006-10-24 2008-05-16 Smithkline Beechman Corp Compuestos derivados de isoxazol sustituidos, agonistas de receptores farnesoid x; procedimiento de preparacion; composicion farmaceutica que lo comprende; y uso del compuesto en el tratamiento de la obesidad, diabetes mellitus, fibrosis en organos,
WO2008073825A1 (en) 2006-12-08 2008-06-19 Exelixis, Inc. Lxr and fxr modulators
US20080300235A1 (en) 2007-06-01 2008-12-04 Wyeth FXR Agonists for Reducing LOX-1 Expression
US20080299118A1 (en) 2007-06-01 2008-12-04 Wyeth FXR Agonists for the Treatment of Malignancies
TW200906823A (en) 2007-07-16 2009-02-16 Lilly Co Eli Compounds and methods for modulating FXR
US8338628B2 (en) 2007-08-28 2012-12-25 City Of Hope Method of synthesizing alkylated bile acid derivatives
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
EP2110374A1 (en) 2008-04-18 2009-10-21 Merck Sante Benzofurane, benzothiophene, benzothiazol derivatives as FXR modulators
EP2289883A1 (en) 2009-08-19 2011-03-02 Phenex Pharmaceuticals AG Novel FXR (NR1H4) binding and activity modulating compounds
HUE039731T2 (hu) * 2009-11-26 2019-01-28 Genfit l,3-difenilprop-2-én-l-on-származékok alkalmazása májbetegségek kezelésére
EP2861613A1 (en) 2012-06-19 2015-04-22 Intercept Pharmaceuticals, Inc. Preparation, uses and solid forms of obeticholic acid
NZ745013A (en) 2012-10-26 2019-08-30 Intercept Pharmaceuticals Inc Process for preparing bile acid derivatives
EP3360881B1 (en) * 2013-05-14 2020-12-09 Intercept Pharmaceuticals, Inc. 11-hydroxyl-6-substituted-derivatives of bile acids and amino acid conjugates thereof as farnesoid x receptor modulators
US10077268B2 (en) * 2014-03-13 2018-09-18 Salk Institute For Biological Studies FXR agonists and methods for making and using
AU2016215179B2 (en) 2015-02-06 2021-02-25 Intercept Pharmaceuticals, Inc. Pharmaceutical compositions for combination therapy

Also Published As

Publication number Publication date
IL253719A0 (en) 2017-09-28
BR112017016766B1 (pt) 2023-11-07
TN2017000344A1 (en) 2019-01-16
CN107405325A (zh) 2017-11-28
AU2016215179B2 (en) 2021-02-25
CO2017007959A2 (es) 2017-10-31
GT201700174A (es) 2018-11-13
AU2016215179A1 (en) 2017-08-24
SV2017005512A (es) 2018-06-12
ECSP17057848A (es) 2017-10-31
EP3253382A4 (en) 2018-10-31
US11311557B2 (en) 2022-04-26
CA2976056C (en) 2024-02-06
WO2016127019A3 (en) 2016-11-03
EP4035665A1 (en) 2022-08-03
CR20170356A (es) 2018-02-28
US20180008616A1 (en) 2018-01-11
KR20170115071A (ko) 2017-10-16
MA40814A1 (fr) 2019-08-30
CL2018001006A1 (es) 2018-06-15
US20220280534A1 (en) 2022-09-08
MX2017010131A (es) 2017-11-01
CL2018003604A1 (es) 2019-02-22
EP3253382B1 (en) 2021-11-17
IL290823A (en) 2022-04-01
BR112017016766A2 (pt) 2018-04-10
DK3253382T3 (da) 2022-02-14
NI201700100A (es) 2018-09-06
EA201791770A1 (ru) 2017-12-29
US20220280533A1 (en) 2022-09-08
ZA201706007B (en) 2019-01-30
PH12017501384A1 (en) 2018-01-08
CA2976056A1 (en) 2016-08-11
TW201628625A (zh) 2016-08-16
CL2017001983A1 (es) 2018-04-20
ES2905872T3 (es) 2022-04-12
IL253719B (en) 2022-04-01
CN107405325B (zh) 2021-11-12
JP2018504438A (ja) 2018-02-15
AU2021201015A1 (en) 2021-03-11
JP2022000483A (ja) 2022-01-04
SG11201706347SA (en) 2017-09-28
PE20180027A1 (es) 2018-01-09
EP3253382A2 (en) 2017-12-13
EA036404B1 (ru) 2020-11-06
HK1246191A1 (zh) 2018-09-07
UA125744C2 (uk) 2022-06-01
WO2016127019A2 (en) 2016-08-11
JP7306791B2 (ja) 2023-07-11

Similar Documents

Publication Publication Date Title
AR103624A1 (es) Composiciones farmacéuticas para terapia de combinación
JP2018504438A5 (es)
SG161256A1 (en) Oral pharmaceutical formulations comprising fenofibric acid and/or its salts
RU2011114992A (ru) 2-арилпропионовые кислоты и производные, и фармацевтические композиции, содержащие указанные соединения
RU2008146815A (ru) Фармацевтическая комбинация, включающая 3-(3-диметиламино-1-этил-2-метилпропил)фенол т нестероидный противовоспалительный препарат
AR097204A1 (es) Métodos de tratamiento de tumores sólidos
PE20121820A1 (es) (2s,3r)-n-(2-((3-piridinil)metil)-1-azabiciclo[2.2.2]oct-3-il)benzofuran-2-carboxamida, formas de sales novedosas de ella, y metodos de uso de ella
CO6710915A2 (es) Composiciones farmacéuticas que contienen un inhibidor de dgat1 ácido 4-(4-(5-6(- trifluorometil-piridin -3- ilamino)-piridin- 2-il)fenil)cicloheiyl)-acético o sales del mismo
CL2011001093A1 (es) Compuestos derivados de 4-[2-(2-fluorofenoximetil)fenil]piperidina, inhibidores de la recaptacion de serotonina y norepinefrina; procedimiento de preparacion; composicion farmaceutica que los comprende; y su uso para tratar el dolor neuropatico, fibromialgia, trastorno depresivo y obesidad entre otras.
UY28468A1 (es) Tableta que contiene el éster etílico de ácido 3-((2-((4-(hexiloxicarbonilamino-imino-metil)-fenilamino)-metil)-1-metil-1h-bencimidazol-5-carbonil)-piridin-2-il-amino)-propiónico o sus sales.
CL2024000758A1 (es) Sal de trometamina de ácido 2-[4-[(5,6-difenilpirazin-2-il)-propan-2-ilamino]butoxi]acético
PE20090243A1 (es) Compuestos de imidazol sustituido como inhibidores de renina
RU2009101326A (ru) Препарат для наружного применения на кожу, содержащий тритерпеновую кислоту
HRP20171425T1 (hr) Derivati oksazolidin-2-on-pirimidina
AR061298A1 (es) Sales de n-hidroxi -3- [4- [ [ [2- (2-metil-1h-indol-3-il) etil] amino] metil] fenil] -2e-2- propenamida.composciones farmaceuticas.
AR065798A1 (es) Usos terapeuticos de la 4-[2-(4-metilfenilsulfanil)fenil]piperidina
PE20141679A1 (es) Derivados de bencil sulfonamida utiles como inhibidores de mogat-2
UY31385A1 (es) Composicion farmacéutica de n-(3-metoxi-5-metilpirazin-2-il)-2-(4-[1,3,4-oxadiazol-2-il]fenil)piridin-3-sulfonamida
MX2010007426A (es) Composiciones farmaceuticas para tratar trastorno del higado graso.
AR052888A1 (es) Uso del agonista alfa de ppar para preparar una formulacion farmaceutica, paquete y dosis unitaria de dicha formulacion
AR080023A1 (es) Formulacion de complejos que comprende aspirina revestida con una barrera que contiene aditivo hidrofobo e inhibidor de la hmg-coa reductasa
PE20080554A1 (es) Formulacion acuosa del acido 4-[((4-carboxibutil)-{2-[(4-fenetilbencil)oxi]fenil}amino)metil]benzoico
IL200959A0 (en) Liquid formulations of salts of 4-[2-(4-methylphenylfanyl)phenyl]piperidine
AR121401A1 (es) Combinaciones de inhibidores de diacilglicerol aciltransferasa 2 e inhibidor de acetil-coa carboxilasa
TW201129557A (en) Pharmaceutical composition for oral administration

Legal Events

Date Code Title Description
FB Suspension of granting procedure