Last reviewed · How we verify
A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Evaluate the Efficacy and Safety of Daily Oral Fasiglifam 25 mg and 50 mg Compared to Placebo When Used in Combination With Sitagliptin in Subjects With Type 2 Diabetes
The purpose of this study is to evaluate the effect of TAK-875 (fasiglifam) in combination with sitagliptin on glycemic control in adults with type 2 diabetes.
Details
| Lead sponsor | Takeda |
|---|---|
| Phase | Phase 3 |
| Status | TERMINATED |
| Enrolment | 90 |
| Start date | 2013-05 |
| Completion | 2014-03 |
Conditions
- Diabetes
Interventions
- Placebo
- TAK-875
- TAK-875
Primary outcomes
- Change From Baseline in HbA1c at Week 24 — Baseline and Week 24
The change in the value of HbA1c (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, Argentina, Peru