Last reviewed · How we verify
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
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 sponsor | Takeda |
|---|---|
| Phase | Phase 3 |
| Status | TERMINATED |
| Enrolment | 33 |
| Start date | 2013-04 |
| Completion | 2014-02 |
Conditions
- Diabetes Mellitus, Type 2
Interventions
- TAK-875
- TAK-875 Placebo
- Glimepiride
Primary outcomes
- Change From Baseline in Glycosylated Hemoglobin (HbA1c) at Week 24 — Baseline and Week 24
The change in the value of glycosylated hemoglobin (the concentration of glucose bound to hemoglobin as a percent of the absolute maximum that can be bound) collected at week 24 relative to baseline.
Countries
United States, Bulgaria, Canada, Hungary, Poland, Romania, Slovakia