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A Randomized, Double-Blind, Active Controlled, Parallel-Group Study to Evaluate the Safety and Efficacy of the Combination BMS-201038 (AEGR-733) and Ezetimibe vs. Monotherapy in Subjects With Moderate Hypercholesterolemia
The main objectives of this study are to evaluate the efficacy and safety of combination therapy BMS-201038 (AEGR-733) plus ezetimibe vs. each agent given alone on LDL cholesterol and other lipoproteins over 12 weeks of therapy.
Details
| Lead sponsor | Aegerion Pharmaceuticals, Inc. |
|---|---|
| Phase | Phase 2 |
| Status | COMPLETED |
| Enrolment | 60 |
| Start date | 2006-05 |
| Completion | 2007-01 |
Conditions
- Hypercholesterolemia
Interventions
- BMS-201038 (AEGR-733)
- Ezetimibe
Primary outcomes
- Percent Change in LDL-C at 12 Weeks Therapy Compared to Baseline Between Treatments — Baseline and 12 weeks of treatment
Countries
United States