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



Status:Completed
Conditions:Diabetes
Therapuetic Areas:Endocrinology
Healthy:No
Age Range:18 - 75
Updated:4/21/2016
Start Date:July 2010
End Date:January 2011

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A Double-blind, Placebo-Controlled, Parallel-group, Randomized, Multiple-Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamic Effects of BMS-823778 in Subjects With Type 2 Diabetes Who Have Inadequate Glycemic Control on Either Diet and Exercise Alone or on a Background of Metformin

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


Inclusion Criteria:

- Type 2 diabetes mellitus

- Drug naive or on stable metformin therapy

- HbA1c 7-10%

- FPG ≤ 240mg/dL

Exclusion Criteria:

- History of myocardial infarction, coronary angioplasty or bypass grafts, valvular
disease or repair, unstable angina pectoris, transient ischemic attack, or
cerebrovascular accidents within six months prior to entry into the study

- Congestive heart failure

- Active liver disease

- Impaired renal function

- Hepatitis C, B and HIV

This list is not inclusive; additional information is provided in the protocol
We found this trial at
4
sites
Olympia, Washington 98502
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Olympia, WA
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Blacktown, New South Wales 2148
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Blacktown,
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Hialeah, Florida 33012
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Hialeah, FL
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Milwaukee, Wisconsin 53209
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Milwaukee, WI
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