Trials / Completed
CompletedNCT01046422
Safety Study of BMS-770767 in Subjects With Type 2 Diabetes
A Double-blind, Placebo-Controlled, Parallel-group, Randomized, Multiple-Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamic Effects of BMS-770767 in Subjects With Type 2 Diabetes Who Have Inadequate Glycemic Control on Either Diet and Exercise Alone or on a Background of Metformin
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 76 (actual)
- Sponsor
- Bristol-Myers Squibb · Industry
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine if BMS-770767 is safe, well tolerated, measure its levels in the blood (pharmacokinetics), and measure the levels of chemicals (biomarkers) that may be affected by this drug (pharmacodynamics) in a type 2 diabetes patient population
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | BMS-770767 | Capsule, Oral, 15mg, Active, Daily, 28 days |
| DRUG | BMS-770767 | Capsule, Oral, 50mg, Active, Daily, 28 days |
| DRUG | BMS-770767 | Capsule, Oral, 150mg, Active, Daily, 28 days |
| DRUG | BMS-770767 | Capsule, Oral, 50mg BID, Active, Daily, 28 days |
| DRUG | Placebo | Capsule, Oral, 0mg, Daily, 28 days |
| DRUG | Metformin | Tablet, Oral, ≥ 1500mg, Active, Daily, 28 days |
Timeline
- Start date
- 2010-05-01
- Primary completion
- 2011-01-01
- Completion
- 2011-01-01
- First posted
- 2010-01-12
- Last updated
- 2015-10-12
Locations
18 sites across 4 countries: United States, Australia, Canada, South Korea
Source: ClinicalTrials.gov record NCT01046422. Inclusion in this directory is not an endorsement.