Study identifier:H8O-BP-GWBG
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
An Open Label Study Comparing Exenatide with Basal Insulin in Achieving an HbA1c of ≤ 7.4% with Minimum Weight Gain, in Type 2 Diabetes Patients who are not Achieving Adequate HbA1c Control on Oral Anti Diabetic Therapies Alone
Type 2 Diabetes
Phase 3
No
exenatide, insulin glargine
All
235
Interventional
30 Years +
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Verified 01 Mar 2015 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
Eli Lilly and Company
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: 1 | Drug: exenatide subcutaneous injection, 5mcg or 10mcg, twice a day Other Name: Byetta |
Active Comparator: 2 | Drug: insulin glargine subcutaneous injection, titrated to target blood glucose level, once a day Other Name: Lantus |