drugset / Trial / NCT00202878

IMPROVE-IT: Examining Outcomes in Subjects With Acute Coronary Syndrome: Vytorin (Ezetimibe/Simvastatin) vs Simvastatin (P04103)

NCT00202878

Phase 3 Completed 18144 enrolled Organon and Co
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a randomized, active-control, double-blind study of subjects with stabilized high-risk acute coronary syndrome (ACS). The primary objective is to evaluate the clinical benefit of Ezetimibe/Simvastatin Combination 10/40 (single tablet, under the brand VYTORIN in the United States) compared with Simvastatin 40 mg. As per the original protocol, if low-density lipoprotein cholesterol (LDL-C) response was inadequate, the dose of simvastatin in the VYTORIN arm or simvastatin arm, could be increased to 80 mg (Note: per June 2011 protocol amendment, criteria for continued use of 80 mg simvastatin were modified and new increases of simvastatin dose to 80 mg were stopped). Clinical benefit will be defined as the reduction in the risk of the occurrence of the composite endpoint of cardiovascular (CV) death, major coronary events, and stroke.

Timeline

Start
2005-10-17
Primary completion
2014-09-18
Completion
2014-09-18

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Simvastatin Small molecule 40 mg
Subject ezetimibe/simvastatin Unknown 10 mg
Subject ezetimibe/simvastatin Unknown 40 mg