Dose Ranging Study of the GLP-1 Agonist AVE0010 in Metformin-Treated Subjects With Type 2 Diabetes Mellitus
Completed · Phase 2
Conditions studied: Type 2 Diabetes
In brief
To evaluate the dose-response relationship of AVE0010 administered once daily and twice daily with chronic dosing in metformin-treated subjects with type 2 diabetes
Key facts
- Study ID
- NCT00299871
- Run by
- Sanofi
- People needed
- 542
- Starts
- 2006-02-01
- Expected to finish
- 2007-08-01
- Last updated by the study team
- 2014-01-28
Who can join
Age: 30 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Males, females, age 30, - 75 years, type 2 diabetes mellitus, treated with metformin ≥1.0 g/day, at a stable dose for at least 3 months, BMI 25 - 40 kg/m2, HbA1C ≥7.0% and <9.0%.
You may not qualify if…
- Type 1 diabetes, pregnancy, lactation, women of childbearing potential, treatment with other antidiabetic agents than metformin, history of metabolic acidosis, hemoglobinopathy or hemolytic anemia, clinically significant medical abnormalities.
Where it is running
- Sanofi-Aventis Administrative Office — Bridgewater, New Jersey, United States
- Sanofi-Aventis Administrative Office — São Paulo, Brazil
- Sanofi-Aventis Administrative Office — Laval, Canada
- Sanofi-Aventis Administrative Office — Warsaw, Poland
- Sanofi-Aventis Administrative Office — Bucharest, Romania
- Sanofi-Aventis Administrative Office — Moscow, Russia
- Sanofi-Aventis Administrative Office — Kiev, Ukraine
Full record on ClinicalTrials.gov
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