Last reviewed · How we verify
A Randomized, Double Blind Comparator-controlled, Parallel-group Study to Evaluate the Safety and Efficacy of the Combination of AEGR-733 and Atorvastatin 20 mg vs Atorvastatin Monotherapy in Subjects With Moderate Hypercholesterolemia
Evaluate the efficacy of combination therapy AEGR-733 plus atorvastatin 20 mg versus monotherapy on serum lipoproteins over 4 and 8 weeks of therapy. The primary efficacy parameter is percent change in LDL-C after 8 weeks of therapy.
Details
| Lead sponsor | Aegerion Pharmaceuticals, Inc. |
|---|---|
| Phase | Phase 2 |
| Status | COMPLETED |
| Enrolment | 44 |
| Start date | 2008-05 |
| Completion | 2008-09 |
Conditions
- Hypercholesterolemia
Interventions
- Atorvastatin
- AEGR-733
Primary outcomes
- Percent Change in LDL-C After 8 Weeks of Therapy — Baseline and 8 weeks of treatment
Countries
United States