JP2014507474A5 - - Google Patents

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Publication number
JP2014507474A5
JP2014507474A5 JP2013557804A JP2013557804A JP2014507474A5 JP 2014507474 A5 JP2014507474 A5 JP 2014507474A5 JP 2013557804 A JP2013557804 A JP 2013557804A JP 2013557804 A JP2013557804 A JP 2013557804A JP 2014507474 A5 JP2014507474 A5 JP 2014507474A5
Authority
JP
Japan
Prior art keywords
pirfenidone
medicament
medicament according
food
patient
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.)
Pending
Application number
JP2013557804A
Other languages
English (en)
Japanese (ja)
Other versions
JP2014507474A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2012/027872 external-priority patent/WO2012122165A2/en
Publication of JP2014507474A publication Critical patent/JP2014507474A/ja
Publication of JP2014507474A5 publication Critical patent/JP2014507474A5/ja
Pending legal-status Critical Current

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JP2013557804A 2011-03-08 2012-03-06 置換n−アリールピリジノン Pending JP2014507474A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201161450489P 2011-03-08 2011-03-08
US61/450,489 2011-03-08
PCT/US2012/027872 WO2012122165A2 (en) 2011-03-08 2012-03-06 Substituted n-aryl pyridinones

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2016244433A Division JP2017057220A (ja) 2011-03-08 2016-12-16 置換n−アリールピリジノン

Publications (2)

Publication Number Publication Date
JP2014507474A JP2014507474A (ja) 2014-03-27
JP2014507474A5 true JP2014507474A5 (OSRAM) 2015-04-09

Family

ID=46798751

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2013557804A Pending JP2014507474A (ja) 2011-03-08 2012-03-06 置換n−アリールピリジノン
JP2016244433A Pending JP2017057220A (ja) 2011-03-08 2016-12-16 置換n−アリールピリジノン

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2016244433A Pending JP2017057220A (ja) 2011-03-08 2016-12-16 置換n−アリールピリジノン

Country Status (9)

Country Link
US (2) US9018232B2 (OSRAM)
EP (1) EP2683379A4 (OSRAM)
JP (2) JP2014507474A (OSRAM)
KR (1) KR20140011355A (OSRAM)
CN (1) CN103561741A (OSRAM)
AU (1) AU2012225611B2 (OSRAM)
BR (1) BR112013022766A2 (OSRAM)
CA (1) CA2828895A1 (OSRAM)
WO (1) WO2012122165A2 (OSRAM)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008157786A1 (en) 2007-06-20 2008-12-24 Auspex Pharmaceutical, Inc. Substituted n-aryl pyridinones as fibrotic inhibitors
US9018232B2 (en) * 2011-03-08 2015-04-28 Auspex Pharmaceuticals, Inc. Substituted N-aryl pyridinones
AR092742A1 (es) 2012-10-02 2015-04-29 Intermune Inc Piridinonas antifibroticas
RU2692485C2 (ru) 2014-04-02 2019-06-25 Интермьюн, Инк. Противофиброзные пиридиноны
CN105315198A (zh) * 2015-11-02 2016-02-10 重庆康乐制药有限公司 一种吡非尼酮的晶型及其制备方法
CN105330598B (zh) * 2015-12-02 2017-11-14 新发药业有限公司 一种吡非尼酮的制备方法
CA2937365C (en) 2016-03-29 2018-09-18 F. Hoffmann-La Roche Ag Granulate formulation of 5-methyl-1-phenyl-2-(1h)-pyridone and method of making the same
CN106748984A (zh) * 2016-11-22 2017-05-31 斯芬克司药物研发(天津)股份有限公司 6‑羟甲基‑1‑苯基吡啶‑2‑酮及其制备方法与应用
US20210267955A1 (en) * 2018-06-29 2021-09-02 Zenvision Pharma Llp Low dose oral pharmaceutical composition of pirfenidone or salt thereof
KR20210076000A (ko) * 2018-09-14 2021-06-23 퓨어테크 엘와이티 100, 아이엔씨. 중수소 농축 피르페니돈 및 이의 사용 방법
CA3171622A1 (en) * 2020-03-13 2021-09-16 Puretech Lyt 100, Inc. Methods of treating respiratory disease with deupirfenidone
EP4499094A1 (en) * 2022-03-31 2025-02-05 Puretech Lyt 100, Inc. Methods of treating interstitial lung diseases and other fibrotic-mediated pulmonary diseases and disorders with deupirfenidone

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JPH02215719A (ja) 1989-02-15 1990-08-28 Yamauchi Akitomo 線維化病変組織の修復並びに線維化病変の阻止剤
US5310562A (en) 1989-11-22 1994-05-10 Margolin Solomon B Composition and method for reparation and prevention of fibrotic lesions
WO1995026325A2 (en) 1994-03-25 1995-10-05 Isotechnika Inc. Enhancement of the efficacy of drugs by deuteration
US6221335B1 (en) 1994-03-25 2001-04-24 Isotechnika, Inc. Method of using deuterated calcium channel blockers
US5962478A (en) 1995-09-19 1999-10-05 Margolin; Solomon B. Inhibition of tumor necrosis factor α
US6294350B1 (en) 1997-06-05 2001-09-25 Dalhousie University Methods for treating fibroproliferative diseases
US6440710B1 (en) 1998-12-10 2002-08-27 The Scripps Research Institute Antibody-catalyzed deuteration, tritiation, dedeuteration or detritiation of carbonyl compounds
DE60001623T2 (de) 1999-12-03 2003-12-18 Pfizer Products Inc., Groton Sulfamoylheteroarylpyrazolverbindungen zur Verwendung als analgetisches/entzündungshemmendes Mittel
EP1134290A3 (en) 2000-03-14 2004-01-02 Pfizer Products Inc. Pharmacophore models for the identification of the CYP2D6 inhibitory potency of selective serotonin reuptake inhibitors
WO2001092188A1 (en) 2000-05-29 2001-12-06 Shionogi & Co., Ltd. Method for labeling with tritium
DE60330126D1 (de) 2002-02-14 2009-12-31 Pharmacia Corp Substituierte pyridinone als modulatoren für p38 map kinase
US20060110358A1 (en) 2002-08-28 2006-05-25 Hsu Henry H Combination therapy for treatment of fibrotic disorders
TW200413273A (en) 2002-11-15 2004-08-01 Wako Pure Chem Ind Ltd Heavy hydrogenation method of heterocyclic rings
EP1599171A2 (en) 2003-02-28 2005-11-30 Intermune, Inc. Combination therapy for treating alphavirus infection and liver fibrosis
WO2004105684A2 (en) 2003-05-16 2004-12-09 Intermune, Inc. Combination therapy for proliferative disorders
WO2005038056A1 (en) 2003-10-14 2005-04-28 Intermune, Inc. Combination therapy for the treatment of viral diseases
WO2005040758A2 (en) 2003-10-24 2005-05-06 Intermune, Inc. Use of pirfenidone in therapeutic regimens
JP4072623B2 (ja) 2004-03-09 2008-04-09 独立行政法人産業技術総合研究所 ピリジン−n−オキシド類の製造方法
WO2005110478A2 (en) 2004-04-13 2005-11-24 Intermune, Inc. Combination therapy for treating fibrotic disorders
PH12012502411A1 (en) 2005-05-10 2019-07-17 Intermune Inc Method of modulating stress-activated protein kinase system
US20080033011A1 (en) 2005-07-29 2008-02-07 Concert Pharmaceuticals Inc. Novel benzo[d][1,3]-dioxol derivatives
NZ591443A (en) 2005-09-22 2013-04-26 Intermune Inc Granule formation of pirfenidone and pharmaceutically acceptable excipients
US20070203202A1 (en) * 2005-12-02 2007-08-30 Robinson Cynthia Y Methods of reducing adverse events associated with pirfenidone therapy
US7750168B2 (en) 2006-02-10 2010-07-06 Sigma-Aldrich Co. Stabilized deuteroborane-tetrahydrofuran complex
CA2661404A1 (en) 2006-09-05 2008-03-13 Schering Corporation Pharmaceutical combinations for lipid management and in the treatment of atherosclerosis and hepatic steatosis
US20080287508A1 (en) * 2007-05-18 2008-11-20 Intermune, Inc. Altering pharmacokinetics of pirfenidone therapy
WO2008157786A1 (en) * 2007-06-20 2008-12-24 Auspex Pharmaceutical, Inc. Substituted n-aryl pyridinones as fibrotic inhibitors
US20090131485A1 (en) * 2007-09-10 2009-05-21 Concert Pharmaceuticals, Inc. Deuterated pirfenidone
JP2012515800A (ja) 2009-01-26 2012-07-12 インターミューン, インコーポレイテッド 急性心筋梗塞および関連障害を処置するための方法
US9018232B2 (en) * 2011-03-08 2015-04-28 Auspex Pharmaceuticals, Inc. Substituted N-aryl pyridinones
AU2012258575B2 (en) * 2011-05-25 2017-03-02 Intermune, Inc. Pirfenidone and anti-fibrotic therapy in selected patients

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