跳至主要内容
临床试验/EUCTR2011-005698-21-PL
EUCTR2011-005698-21-PL进行中(未招募)1 期

A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Effect of Alirocumab (SAR236553/REGN727) on the Occurrence of Cardiovascular Events in Patients Who Have Recently Experienced an Acute Coronary Syndrome - Odyssey Outcomes

sanofi-aventis Recherche & Développement0 个研究点目标入组 18,600 人开始时间: 2013年2月25日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
18,600

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • o Recently (<52 weeks) hospitalized for ACS.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 16000
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 2600

排除标准

  • o Age < 40 years.
  • o ACS event occurring more than 52 weeks prior to randomization visit.
  • o LDL-C likely to be <70 mg/dL (<1.81 mmo/L) with evidence-based medical and dietary management of dyslipidemia.

研究者

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