A Study of DPP-IV Inhibitor in Patients With Type 2 Diabetes
Completed · Phase 2 · Has a placebo group
Conditions studied: Diabetes Mellitus Type 2
In brief
This study will assess the efficacy, safety and tolerability of DPP-IV Inhibitor in patients with type 2 diabetes receiving a stable dose of metformin. The anticipated time on study treatment is 3-12 months and the target sample size is 100-500 individuals.
Key facts
- Study ID
- NCT00111631
- Run by
- Hoffmann-La Roche
- People needed
- 218
- Starts
- 2005-05-01
- Expected to finish
- 2006-10-01
- Last updated by the study team
- 2016-11-02
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- adult patients 18-75 years of age;
- type 2 diabetes;
- stable metformin therapy for >=3 months before screening.
You may not qualify if…
- women who are pregnant, breast-feeding, or not using an adequate contraceptive method;
- type 1 diabetes;
- any anti-hyperglycemic medication other than metformin in the last 3 months.
Where it is running
- Study site — Concord, California, United States
- Study site — Salinas, California, United States
- Study site — San Diego, California, United States
- Study site — Boulder, Colorado, United States
- Study site — Newark, Delaware, United States
- Study site — Wilmington, Delaware, United States
- Study site — Clearwater, Florida, United States
- Study site — Miami, Florida, United States
- Study site — Chicago, Illinois, United States
- Study site — Detroit, Michigan, United States
- Study site — Buffalo, New York, United States
- Study site — Rochester, New York, United States
- Study site — Durham, North Carolina, United States
- Study site — Mogadore, Ohio, United States
- Study site — Portland, Oregon, United States
- Study site — Connellsville, Pennsylvania, United States
- Study site — Warminster, Pennsylvania, United States
- Study site — Dallas, Texas, United States
- Study site — Midland, Texas, United States
- Study site — San Antonio, Texas, United States
- Study site — Adelaide, Australia
- Study site — Sydney, Australia
- Study site — Winnipeg, Manitoba, Canada
- Study site — Halifax, Nova Scotia, Canada
- Study site — London, Ontario, Canada
Full record on ClinicalTrials.gov
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