drugset / Trial / NCT01111955

Safety Study of BMS-823778 in Subjects With Type 2 Diabetes

NCT01111955 ↗

Phase 2 Completed 62 enrolled Bristol-Myers Squibb
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to assess the safety, tolerability and pharmacodynamic effects on fasting plasma glucose (FPG).

Timeline

Start
2010-07
Primary completion
2011-01
Completion
2011-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator BMS-823778 Small molecule 2 mg Oral
Comparator BMS-823778 Small molecule 10 mg Oral
Comparator BMS-823778 Small molecule 20 mg Oral
Comparator Metformin Small molecule 1500 mg Oral