drugset / Trial / NCT01124344

Safety and Pharmacology Study of BMS-866949

NCT01124344 ↗

Phase 1 Terminated 47 enrolled Bristol-Myers Squibb
RandomizedParallel-groupDouble-blindTreatment

Summary

The main purpose of this study is to determine whether multiple doses.of BMS-886949 are safe and tolerable

Timeline

Start
2010-05
Primary completion
2011-11
Completion
2011-11

Drugs

EvaluationDrugModalityDoseRoute
Comparator BMS-866949 Unknown 3 mg Oral
Comparator BMS-866949 Unknown 10 mg Oral
Comparator BMS-866949 Unknown 30 mg Oral
Comparator BMS-866949 Unknown 45 mg Oral
Comparator BMS-866949 Unknown 60 mg Oral
Comparator BMS-866949 Unknown 90 mg Oral