drugset / Trial / NCT00243308

Serp-1 for the Treatment of Acute Coronary Syndrome

NCT00243308 ↗

Phase 2 Terminated 72 enrolled Viron Therapeutics Inc
RandomizedParallel-groupDouble-blindDiagnostic

Summary

Males and females aged 18-80 years who present with ACS (unstable angina and non ST-elevation MI) defined as one or more episodes of angina lasting at least 5 minutes in the last 24 hours before admission and greater than 0.05 mV of presumed new ST-segment depression in at least 2 contiguous ECG leads OR, angina and per confirmatory angiogram, has been scheduled for percutaneous coronary angioplasty. The primary objective of this study is to evaluate the safety of Serp-1 injection when administered in 3 daily doses to patients undergoing conventional therapy for Acute Coronary Syndrome (ACS) requiring early intervention.

Timeline

Start
2005-10
Primary completion
2008-07
Completion
2008-12

Outcome

Outcome not reported

Stopped (Enrollment): “Third dose group not recruited due to slow enrollment.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Serp-1 Protein / enzyme biologic 5 ug/kg Intravenous
Subject Serp-1 Protein / enzyme biologic 15 ug/kg Intravenous
Subject Serp-1 Protein / enzyme biologic 50 ug/kg Intravenous