drugset / Trial / NCT01112423

Safety Study of BMS-823778 in Subjects With Hypercholesterolemia

NCT01112423 ↗

Phase 2 Completed 60 enrolled Bristol-Myers Squibb
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to assess the safety, tolerability and pharmacodynamic effects on LDL cholesterol (LDL-C)

Timeline

Start
2010-06
Primary completion
2010-12
Completion
2010-12

Drugs

EvaluationDrugModalityDoseRoute
Subject BMS-823778 Small molecule 2 mg Oral
Subject BMS-823778 Small molecule 10 mg Oral
Subject BMS-823778 Small molecule 20 mg Oral

Indications