Study of the Safety of Substituting Exenatide for Insulin in Patients Using Insulin and Oral Antidiabetic Agents
Completed · Phase 2
Conditions studied: Type 2 Diabetes Mellitus
In brief
This study will look at the safety of substituting exenatide for insulin in patients with type 2 diabetes who are currently taking insulin and oral antidiabetic agent(s).
Key facts
- Study ID
- NCT00099333
- Run by
- AstraZeneca
- People needed
- 49
- Starts
- 2004-02-01
- Expected to finish
- 2005-08-01
- Last updated by the study team
- 2015-02-23
Who can join
Age: 35 and older, up to 70. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients have been treated with insulin for >=3 months up to 12 years.
- HbA1c <=10.5%.
- Body mass index (BMI) between 27 kg/m2 and 40 kg/m2.
You may not qualify if…
- Patients previously received exenatide or GLP-1 analogs.
- Patients have been treated for greater than 2 weeks with thiazolidinediones or alpha-glucosidase inhibitors within 3 months prior to screening.
Where it is running
- Research Site — Chula Vista, California, United States
- Research Site — Butte, Montana, United States
- Research Site — Portland, Oregon, United States
- Research Site — Nashville, Tennessee, United States
- Research Site — San Antonio, Texas, United States
Full record on ClinicalTrials.gov
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