LivingGLP1
Study S003397

Phase 2/3, Randomized, Double-blind, Placebo- and Active Comparator-controlled, Parallel, Multicenter Study to Determine Safety and Efficacy of Metaglidasen in Treatment of Type 2 Diabetes Suboptimally Controlled on Insulin

Registration

Registration
NCT00353587
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2; PHASE3
Masking
DOUBLE
Status
COMPLETED
Enrollment
396
Start
2006-05
Primary completion
2007-11
Lead sponsor
Gilead Sciences
Conditions
Type 2 Diabetes
Interventions
DRUG:MBX-102; DRUG:Placebo; DRUG:Actos
Results posted
FALSE

Registered primary outcomes

  • Evaluate effects of MBX-102 administered orally at doses of 200, 400 and 600 mg daily for 16 weeks, on glucose control, as measured by HbA1c []
  • Evaluate safety of MBX-102 with particular emphasis on endpoints of weight gain and edema []

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