JP2008050367A5 - - Google Patents

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JP2008050367A5
JP2008050367A5 JP2007287366A JP2007287366A JP2008050367A5 JP 2008050367 A5 JP2008050367 A5 JP 2008050367A5 JP 2007287366 A JP2007287366 A JP 2007287366A JP 2007287366 A JP2007287366 A JP 2007287366A JP 2008050367 A5 JP2008050367 A5 JP 2008050367A5
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composition according
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cardiovascular
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JP2008050367A (en
JP5134916B2 (en
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イコサペント酸エチルエステルを有効成分として含有する、
心血管再建術施行後不安定期を経過した後に起こる心血管イベントの発症を予防するための心血管イベント予防用組成物。
Containing ethyl icosapentate as an active ingredient,
A composition for preventing cardiovascular events for preventing the onset of a cardiovascular event that occurs after an unstable period has elapsed after cardiovascular reconstruction.
心血管再建術施行後不安定期を経過した後に投与を開始する請求項1に記載の組成物。   The composition according to claim 1, wherein administration is started after an unstable period has elapsed after cardiovascular reconstruction. イコサペント酸エチルエステルを有効成分として含有する、
心血管再建術施行後6ヶ月を経過した後の患者のための心血管イベント発症を予防する心血管イベント予防用組成物。
Containing ethyl icosapentate as an active ingredient,
A composition for preventing cardiovascular events, which prevents the onset of cardiovascular events for a patient who has passed 6 months after cardiovascular reconstruction.
前記患者が、心筋梗塞発症後6か月以内の患者を除いた患者である、請求項3に記載の組成物。The composition according to claim 3, wherein the patient is a patient excluding a patient within 6 months after the onset of myocardial infarction. 心血管再建術施行後6ヶ月を経過した後に投与を開始し、少なくとも2年以上継続して投与することを特徴とする請求項1ないしのいずれかに記載の組成物。 The composition according to any one of claims 1 to 4 , wherein the administration is started after 6 months have passed since the execution of cardiovascular reconstruction, and the administration is continued for at least 2 years. 心血管再建術が、経皮的冠動脈内腔拡張術(PTCA)、経皮的冠動脈内血栓溶解術(PTCR)、方向性冠動脈粥種切除術(DCA)、冠動脈ステント留置術、冠動脈バイパス術(ACバイパス術)である請求項1ないしのいずれかに記載の組成物。 Cardiovascular reconstruction includes percutaneous coronary lumen dilatation (PTCA), percutaneous intracoronary thrombolysis (PTCR), directional coronary angioplasty (DCA), coronary stenting, coronary artery bypass surgery ( The composition according to any one of claims 1 to 5 , wherein the composition is AC bypass. 前記患者が、高脂血症であることを特徴とする請求項1ないしのいずれかに記載の組成物。 The composition according to any one of claims 1 to 6 , wherein the patient has hyperlipidemia. 前記患者の血清T−Cho濃度が、220mg/dl以上、および/または、血清LDL−Cho濃度が140mg/dl以上である請求項7に記載の組成物。The composition according to claim 7, wherein the patient has a serum T-Cho concentration of 220 mg / dl or more and / or a serum LDL-Cho concentration of 140 mg / dl or more. 全脂肪酸およびその誘導体中のイコサペント酸エチルエステル含量比が96.5重量%以上である請求項1ないしのいずれかに記載の組成物。 The composition according to any one of claims 1 to 8 , wherein the content ratio of ethyl ester of icosapentate in all fatty acids and derivatives thereof is 96.5% by weight or more. イコサペント酸エチルエステル1.8g/日〜2.7g/日で経口投与することを特徴とする請求項1ないしのいずれかに記載の組成物。 The composition according to any one of claims 1 to 9 , wherein the composition is orally administered at 1.8 g / day to 2.7 g / day of icosapentic acid ethyl ester. 3−ヒドロキシ−3−メチルグルタリルコエンザイムA還元酵素阻害剤と併用することを特徴とする請求項1ないし10のいずれかに記載の組成物。The composition according to any one of claims 1 to 10, which is used in combination with a 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor. 3−ヒドロキシ−3−メチルグルタリルコエンザイムA還元酵素阻害剤が、プラバスタチン、シンバスタチン、および、アトルバスタチンからなる群から選択される1以上である、請求項11に記載の組成物。The composition according to claim 11, wherein the 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor is one or more selected from the group consisting of pravastatin, simvastatin, and atorvastatin. 3−ヒドロキシ−3−メチルグルタリルコエンザイムA還元酵素阻害剤の1日当たりの投与量が、プラバスタチン5〜20mg/日、シンバスタチン2.5〜20mg/日、または、アトルバスタチン5〜40mg/日である請求項12に記載の組成物。The daily dose of the 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor is pravastatin 5-20 mg / day, simvastatin 2.5-20 mg / day, or atorvastatin 5-40 mg / day Item 13. The composition according to Item 12.
JP2007287366A 2005-07-08 2007-11-05 Composition for preventing cardiovascular events Active JP5134916B2 (en)

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JP2007287366A JP5134916B2 (en) 2005-07-08 2007-11-05 Composition for preventing cardiovascular events

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JP2005200503 2005-07-08
JP2005200503 2005-07-08
JP2007287366A JP5134916B2 (en) 2005-07-08 2007-11-05 Composition for preventing cardiovascular events

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JP2006188456A Division JP4751257B2 (en) 2005-07-08 2006-07-07 Composition for preventing cardiovascular events

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JP2012157914A Division JP5809115B2 (en) 2005-07-08 2012-07-13 Preparation for cardiovascular event prevention

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JP2008050367A JP2008050367A (en) 2008-03-06
JP2008050367A5 true JP2008050367A5 (en) 2009-08-13
JP5134916B2 JP5134916B2 (en) 2013-01-30

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Families Citing this family (16)

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Publication number Priority date Publication date Assignee Title
US20110236476A1 (en) 2008-09-02 2011-09-29 Amarin Corporation Plc. Pharmaceutical composition comprising eicosapentaenoic acid and nicotinic acid and methods of using same
NZ624963A (en) 2009-04-29 2016-07-29 Amarin Pharmaceuticals Ie Ltd Pharmaceutical compositions comprising epa and a cardiovascular agent and methods of using the same
NZ627238A (en) 2009-04-29 2016-02-26 Amarin Pharmaceuticals Ie Ltd Stable pharmaceutical composition comprising ethyl eicosapentaenoate
MY172372A (en) 2009-06-15 2019-11-21 Amarin Pharmaceuticals Ie Ltd Compositions and methods for lowering triglycerides
NZ744990A (en) 2010-11-29 2019-10-25 Amarin Pharmaceuticals Ie Ltd Low eructation composition and methods for treating and/or preventing cardiovascular disease in a subject with fish allergy/hypersensitivity
US11712429B2 (en) 2010-11-29 2023-08-01 Amarin Pharmaceuticals Ireland Limited Low eructation composition and methods for treating and/or preventing cardiovascular disease in a subject with fish allergy/hypersensitivity
US11291643B2 (en) 2011-11-07 2022-04-05 Amarin Pharmaceuticals Ireland Limited Methods of treating hypertriglyceridemia
EP2866801A4 (en) 2012-06-29 2016-02-10 Amarin Pharmaceuticals Ie Ltd Methods of reducing the risk of a cardiovascular event in a subject on statin therapy
WO2014074552A2 (en) 2012-11-06 2014-05-15 Amarin Pharmaceuticals Ireland Limited Compositions and methods for lowering triglycerides without raising ldl-c levels in a subject on concomitant statin therapy
US20140187633A1 (en) 2012-12-31 2014-07-03 Amarin Pharmaceuticals Ireland Limited Methods of treating or preventing nonalcoholic steatohepatitis and/or primary biliary cirrhosis
US9452151B2 (en) 2013-02-06 2016-09-27 Amarin Pharmaceuticals Ireland Limited Methods of reducing apolipoprotein C-III
US9624492B2 (en) 2013-02-13 2017-04-18 Amarin Pharmaceuticals Ireland Limited Compositions comprising eicosapentaenoic acid and mipomersen and methods of use thereof
US9283201B2 (en) 2013-03-14 2016-03-15 Amarin Pharmaceuticals Ireland Limited Compositions and methods for treating or preventing obesity in a subject in need thereof
US9585859B2 (en) 2013-10-10 2017-03-07 Amarin Pharmaceuticals Ireland Limited Compositions and methods for lowering triglycerides without raising LDL-C levels in a subject on concomitant statin therapy
WO2015195662A1 (en) 2014-06-16 2015-12-23 Amarin Pharmaceuticals Ireland Limited Methods of reducing or preventing oxidation of small dense ldl or membrane polyunsaturated fatty acids
KR102296068B1 (en) 2018-09-24 2021-09-02 애머린 파마슈티칼스 아일랜드 리미티드 Methods of Reducing the Risk of a Cardiovascular Event in a Subject

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US5861399A (en) * 1996-07-17 1999-01-19 Heart Care Partners Methods and compositions for the rapid and enduring relief of inadequate myocardial function
IT1308613B1 (en) * 1999-02-17 2002-01-09 Pharmacia & Upjohn Spa ESSENTIAL FATTY ACIDS IN THE PREVENTION OF CARDIOVASCULAR EVENTS.
ITMI20012384A1 (en) * 2001-11-12 2003-05-12 Quatex Nv USE OF POLYUNSATURATED FATTY ACIDS FOR THE PRIMARY PREVENTION OF MAJOR CARDIOVASCULAR EVENTS
JP2006519244A (en) * 2003-03-05 2006-08-24 ゾルファイ ファーマスーティカルズ ゲゼルシャフト ミット ベシュレンクテル ハフツング Use of omega-3-fatty acids in the treatment of diabetic patients
JP4751257B2 (en) * 2005-07-08 2011-08-17 持田製薬株式会社 Composition for preventing cardiovascular events

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