drugset / Trial / NCT00461630

Treatment of HDL to Reduce the Incidence of Vascular Events HPS2-THRIVE

NCT00461630

Phase 3 Completed 25673 enrolled University of Oxford Merck Sharp & Dohme LLC · collab
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The primary aim is to assess the effects of raising HDL cholesterol (the good type) with extended release niacin/laropiprant 2g (previously known as MK-0524A) versus matching placebo on the risk of heart attack or coronary death, stroke, or the need for arterial bypass procedures (revascularisation) in people with a history of circulatory problems. The secondary aim is to assess the effects of extended release niacin/laropiprant 2g daily on heart attack, coronary death, stroke, and revascularisation separately and to assess the effects on mortality both overall and in various categories of causes of death, and of the effects on major cardiovascular events in people with a history of different diseases at the beginning of the study.

Timeline

Start
2007-01
Primary completion
2012-10
Completion
2012-10

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Niacin Small molecule 2 g Oral
Subject laropiprant Small molecule 40 mg Oral
Background Ezetimibe Unknown 10 mg Oral
Background Simvastatin Small molecule 40 mg Oral