drugset / Trial / NCT01587235

A Study to Evaluate the Efficacy and Safety of Vytorin Versus Standard Treatment of Other Statins in Moderate, Moderately High and High Risk Participants (MK-0653A-406)

NCT01587235 ↗

Phase 4 Withdrawn Organon and Co
RandomizedParallel-groupOpen-labelTreatment

Summary

This study will evaluate and compare the effectiveness of MK-0653 (Vytorin) to current standard treatment with other statins for the treatment of dyslipidemia in moderate, moderately-high and high-risk participants.

Timeline

Start
2013-03
Primary completion
2014-05
Completion
2014-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Ezetimibe/simvastatin Unknown 10 mg Oral
Subject Ezetimibe/simvastatin Unknown 20 mg Oral
Subject Ezetimibe/simvastatin Unknown 40 mg Oral

Indications