drugset / Trial / NCT00685776

Study to Assess the Tolerability and Efficacy of Anacetrapib in Patients With Coronary Heart Disease (CHD) or CHD Risk-Equivalent Disease (MK-0859-019)

NCT00685776 ↗

Phase 3 Completed 1623 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupDouble-blindTreatment

Summary

This study will evaluate the efficacy of anacetrapib (100 mg) for 24 weeks relative to placebo, on plasma concentrations of Low Density Lipoprotein Cholesterol and assess the safety and tolerability of anacetrapib (100 mg) in participants with CHD/CHD risk-equivalent disease on stable dose regimen of statin with or without other lipid-modifying therapy. The two year extension to this study will further evaluate the long-term safety profile and efficacy of anacetrapib in CHD/CHD-risk equivalent patients who are on ongoing therapy with a statin with or without other lipid-modifying therapy.

Timeline

Start
2008-03-24
Primary completion
2009-07-02
Completion
2017-11-23

Outcome

Met primary endpoint

paper in the placebo group (P<0.001)--a 39.8% reduction with anacetrapib beyond that seen with placebo. PMID 21082868 ↗

paper Treatment with anacetrapib had robust effects on LDL and HDL cholesterol, had an acceptable side-effect profile PMID 21082868 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Anacetrapib Small molecule 100 mg —