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Clinical Trials/NL-OMON38390
NL-OMON38390
Completed
Phase 2

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 sites80 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Acute Coronary Syndrome
Sponsor
Cerenis Therapeutics SA
Enrollment
80
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
Cerenis Therapeutics SA

Eligibility Criteria

Inclusion Criteria

  • 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.

Exclusion Criteria

  • 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%.

Outcomes

Primary Outcomes

Not specified

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