Ezetimibe Plus Simvastatin Versus Simvastatin in Patients With Hypercholesterolemia and Coronary Risk Factors (P03405)

• Status: Terminated
• Trial end date: 2006-06-01
• Target enrollment: 0
• Participant gender: All

Summary

The study was designed to assess whether 6 weeks of co-administration of ezetimibe and simvastatin is more effective than simvastatin monotherapy in allowing patients in the CHD risk strata of the NCEP III guidelines to achieve their LDL-C target goal of <=3.0 mmol/L. As this study was to be conducted in Canada, the target LDL-C goal for patients with CHD, or type II diabetic patients >30 years old with no CHD, was <2.5 mmol/L.

• Phase: Phase 4
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Merck Sharp & Dohme Corp.
• Collaborator: Merck Frosst Canada Ltd.
• Treatments: Ezetimibe; Simvastatin

Criteria

Inclusion Criteria:

• >=18 years of age and treated with simvastatin 10 mg or 20 mg for at least 6 weeks and LDL-C levels of > 2.5 mmol/L to <=4.20 mmol/L (97 mg/dL to 160 mg/dL) at Visit 1.

• history of coronary heart disease (type II diabetic patients > 30 years old with no CHD)

• triglycerides <= 4.00 mmol/L drawn, and liver transaminases (ALT, AST) <=50% above the upper limit of normal at Visit 2, with no active liver disease, and/or creatine kinase (CK) <=50% above the upper limit of normal

Exclusion Criteria:

• subjects with Body Mass Index >=35 kg/sqm at Visit 1

• alcohol consumption > 14 drinks per week

• pregnant or lactating

• treated with any other investigational drug within 30 days prior Visit 1

• previously treated with ezetimibe or participated in a clinical study with ezetimibe

• any condition or situation which, in the opinion of the investigator, might pose a risk to the patient or interfere with participation in the study