drugset / Trial / NCT01240980

Safety Study of BMS-903452 in Healthy Subjects (Panel 1-7) & Relative Bioavailability of the Crystalline and Amorphous Forms of BMS-903452 [Panels 4, 6, 11 & 12(Part A)], and Subjects With Type 2 Diabetes Mellitus (Part B)

NCT01240980 ↗

Phase 1 Completed 104 enrolled Bristol-Myers Squibb
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability and effect on blood glucose control of BMS-903452 compared to placebo in healthy subjects \& relative bioavailability of the crystalline and amorphous forms of BMS-903452 \[Panels 4,6,11 \& 12(Part A)\] ; and subjects with type 2 Diabetes Mellitus (Part B). The study will also determine the amount of BMS-903452 in the blood.

Timeline

Start
2010-11
Primary completion
2012-01
Completion
2012-01

Drugs

EvaluationDrugModalityDoseRoute
Subject BMS-903452 Small molecule 0.1 mg Oral
Subject BMS-903452 Small molecule 0.6 mg Oral
Subject BMS-903452 Small molecule 3 mg Oral
Subject BMS-903452 Small molecule 10 mg Oral
Subject BMS-903452 Small molecule 30 mg Oral
Subject BMS-903452 Small molecule 60 mg Oral
Subject BMS-903452 Small molecule 120 mg Oral

Indications