跳至主要内容
临床试验/EUCTR2010-023611-34-NL
EUCTR2010-023611-34-NL进行中(未招募)不适用

A Phase II Multi-Center, Double-Blind, Ascending Dose, Placebo-Controlled, Dose-Finding Trial of CER-001 or Placebo in Subjects with Acute Coronary Syndrome - CHI SQUARE

Cerenis Therapeutics0 个研究点目标入组 500 人开始时间: 2011年5月3日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
500

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

  • Male or female under 75 years of age, acute chest pain and diagnosis of ST segment elevation or non-ST elevation myocardial infarction or unstable angina, clinically indicated coronary angiography, evidence of coronary artery disease, and an appropriate target coronary artery.
  • 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
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Subjects weighing more than 120 kg, uncontrolled diabetes, triglycerides greater than 500 mg/dl, baseline IVUS of unacceptable quality, subjects for whom CABG is planned, hemodynamically or clinically unstable, and ejection fraction less than 35%.

研究者

发起方
Cerenis Therapeutics

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