跳至主要内容
临床试验/NL-OMON38390
NL-OMON38390已完成2 期

Can HDL Infusions Significantly Quicken Atherosclerosis Regression? 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 Therapeutics SA0 个研究点目标入组 80 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
80

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • male or female up to and including 80 years of age, acute chest pain and diagnosis of ST segment elevation or non-ST elevation myocadial infarction or unstable angina, clincally indicated coranary angiography, evidence of coronary artery disease, and an appropriate target coronary artery.

排除标准

  • Subjects weighing more than 160 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 ejcection fraction less than 35%.

研究者

发起方
Cerenis Therapeutics SA

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