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A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled, 24-Week Study to Evaluate the Efficacy and Safety of Daily Oral TAK-875 50 mg Compared With Placebo as an Add-on to Glimepiride in Subjects With Type 2 Diabetes

NCT01829477 Phase 3 TERMINATED Results posted

The purpose of this study is to evaluate the effect of TAK-875 compared to placebo on glycemic control over a 24-week Treatment Period when used as an add-on to glimepiride in addition to diet and exercise.

Details

Lead sponsorTakeda
PhasePhase 3
StatusTERMINATED
Enrolment33
Start date2013-04
Completion2014-02

Conditions

Interventions

Primary outcomes

Countries

United States, Bulgaria, Canada, Hungary, Poland, Romania, Slovakia