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 (enExample) 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 (enExample)
EP (1) EP2683379A4 (enExample)
JP (2) JP2014507474A (enExample)
KR (1) KR20140011355A (enExample)
CN (1) CN103561741A (enExample)
AU (1) AU2012225611B2 (enExample)
BR (1) BR112013022766A2 (enExample)
CA (1) CA2828895A1 (enExample)
WO (1) WO2012122165A2 (enExample)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
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CA2691379C (en) 2007-06-20 2015-06-09 Auspex Pharmaceuticals, Inc. Substituted n-aryl pyridinones
CN103561741A (zh) * 2011-03-08 2014-02-05 奥斯拜客斯制药有限公司 取代的n-芳基吡啶酮
AR092742A1 (es) 2012-10-02 2015-04-29 Intermune Inc Piridinonas antifibroticas
US10233195B2 (en) 2014-04-02 2019-03-19 Intermune, Inc. Anti-fibrotic pyridinones
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
WO2020003107A1 (en) * 2018-06-29 2020-01-02 Zenvision Pharma Llp Low dose oral pharmaceutical composition of pirfenidone or salt thereof
CN121108041A (zh) 2018-09-14 2025-12-12 纯技术莱特100股份有限公司 富含氘的吡非尼酮及其使用方法
US20250114341A1 (en) 2018-09-14 2025-04-10 Puretech Lyt 100, Inc. Methods of treating idiopathic pulmonary fibrosis with deupirfenidone
CA3171622A1 (en) 2020-03-13 2021-09-16 Puretech Lyt 100, Inc. Methods of treating respiratory disease with deupirfenidone
JP2025511066A (ja) * 2022-03-31 2025-04-15 ピュアテック・エル・ワイ・ティ・100・インコーポレイテッド デューピルフェニドンにより間質性肺疾患ならびに他の線維化介在性肺疾患及び障害を治療する方法

Family Cites Families (31)

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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
CN1087725C (zh) 1994-03-25 2002-07-17 同位素技术有限公司 用氘代方法增强药物效果
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
DK1104760T3 (da) 1999-12-03 2003-06-30 Pfizer Prod Inc Sulfamoylheteroarylpyrazolforbindelser som anti-inflammatoriske/analgetiske midler
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
US20030194748A1 (en) 2000-05-29 2003-10-16 Tohru Nagasaki Method for labeling with tritium
ES2334990T3 (es) 2002-02-14 2010-03-18 Pharmacia Corporation Piridinonas sustituidas como moduladores de p38 map quinasa.
AU2003258305A1 (en) 2002-08-28 2004-03-19 Intermune, Inc. 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
US20070072181A1 (en) 2003-02-28 2007-03-29 Blatt Lawrence M 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
US7407973B2 (en) 2003-10-24 2008-08-05 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
MX2007014114A (es) 2005-05-10 2008-03-14 Intermune Inc Derivados de piridona para modular el sistema de proteina cinasa activada por estres.
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
US20080103122A1 (en) 2006-09-05 2008-05-01 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
CA2691379C (en) 2007-06-20 2015-06-09 Auspex Pharmaceuticals, Inc. Substituted n-aryl pyridinones
WO2009035598A1 (en) 2007-09-10 2009-03-19 Concert Pharmaceuticals, Inc. Deuterated pirfenidone
EP2389227A4 (en) 2009-01-26 2012-08-08 Intermune Inc METHOD FOR THE TREATMENT OF ACUTE MYOCARDINE CARDS AND ASSOCIATED ILLNESSES THEREOF
CN103561741A (zh) * 2011-03-08 2014-02-05 奥斯拜客斯制药有限公司 取代的n-芳基吡啶酮
KR20140022048A (ko) * 2011-05-25 2014-02-21 인터뮨, 인크. 선택된 환자에서의 피르페니돈 및 항-섬유성 치료제

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