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
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 []
Linked records (0)
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