LivingGLP1
Study S002334

Randomized, Placebo-Controlled, Single-Dose, Crossover Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of BMS-686117 in Subjects With Type 2 Diabetes

Registration

Registration
NCT00508287
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE1
Masking
DOUBLE
Status
COMPLETED
Enrollment
36
Start
2007-08
Primary completion
2007-11
Lead sponsor
Bristol-Myers Squibb
Conditions
Type 2 Diabetes
Interventions
DRUG:BMS-686117; DRUG:Byetta; DRUG:Placebo
Results posted
FALSE

Registered primary outcomes

  • Safety: incidence of adverse events [from subject enrollment to study discharge]

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