drugset / Trial / NCT00529178

Pravastatin Efficacy and Safety Trial in Hypercholesterolemic Patients With Chronic Liver Disease

NCT00529178

Phase 4 Completed 232 enrolled Bristol-Myers Squibb
RandomizedParallel-groupDouble-blindTreatment

Summary

To determine in hypercholesterolemic subjects with chronic, well-compensated liver disease, the percent change from baseline to Week 12 in serum LDL-C of pravastatin 80 mg compared to placebo.

Timeline

Start
2002-12
Primary completion
2005-03
Completion
2005-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Pravastatin Small molecule 80 mg

Indications