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A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Determine the Efficacy and Safety of SYR110322 (SYR-322) When Used in Combination With a Sulfonylurea in Subjects With Type 2 Diabetes
The purpose of this study is to evaluate the efficacy and safety of alogliptin, once daily (QD), combined with a sulfonylurea in adults with type 2 diabetes mellitus.
Details
| Lead sponsor | Takeda |
|---|---|
| Phase | Phase 3 |
| Status | COMPLETED |
| Enrolment | 500 |
| Start date | 2006-04 |
| Completion | 2007-06 |
Conditions
- Diabetes Mellitus
Interventions
- Alogliptin and glyburide
- Alogliptin and glyburide
- Glyburide
Primary outcomes
- Change From Baseline in Glycosylated Hemoglobin (HbA1c) at Week 26. — Baseline and Week 26.
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 26 or final visit and glycosylated hemoglobin collected at baseline.
Countries
United States, Argentina, Australia, Brazil, Chile, Dominican Republic, Guatemala, India, Mexico, Netherlands, New Zealand, Peru, Poland, South Africa, United Kingdom