Overview
Study of the Safety of Substituting Exenatide for Insulin in Patients Using Insulin and Oral Antidiabetic Agents
Status:
Completed
Completed
Trial end date:
2005-08-01
2005-08-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
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).Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
AstraZenecaCollaborator:
Eli Lilly and CompanyTreatments:
Exenatide
Hypoglycemic Agents
Insulin
Insulin, Globin Zinc
Criteria
Inclusion Criteria:- 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.
Exclusion Criteria:
- 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.