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非スタチン系脂質修飾療法または最低強度のスタチンでコレステロール値が十分にコントロールされていない高コレステロール血症患者におけるアリロクマブの有効性および安全性

基本情報

NCT ID
NCT02584504
ステータス
完了
試験のフェーズ
第3相
試験タイプ
介入
目標被験者数
163
治験依頼者名
Sanofi

概要

Primary Objective: To demonstrate the reduction of low-density lipoprotein cholesterol (LDL-C) by alirocumab administration as add-on therapy to non-statin lipid modifying therapy (LMT) including diet therapy alone or the lowest strength of statin in comparison with placebo after 12 weeks of treatment in participants with hypercholesterolemia. Secondary Objective: * To evaluate the effect of two treatment regimens of alirocumab on other lipid parameters: apolipoprotein B (Apo-B), non-high-density lipoprotein cholesterol (non HDL-C), total cholesterol (TC), lipoprotein (a) (Lp\[a\]), high-density lipoprotein cholesterol (HDL-C), triglyceride (TG), and apolipoprotein A-1 (Apo A-1). * To evaluate the safety and tolerability of alirocumab administration. * To evaluate the development of anti-alirocumab antibodies. * To evaluate the pharmacokinetic and pharmacodynamic profiles of alirocumab administration. * To evaluate the long-term safety in participants receiving open-label alirocumab administration.

対象疾患

Hypercholesterolemia

介入

Alirocumab(DRUG)
Placebo(DRUG)
Atorvastatin(DRUG)
Non-statin Lipid-Modifying Therapy(DRUG)
Diet Alone(OTHER)

依頼者(Sponsor)