Study identifier:H8O-JE-GWBX
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
Parallel Group Study to Evaluate the Efficacy and Safety of Exenatide Once-Weekly Injection Compared to Once-Daily Insulin in Type 2 Diabetes Mellitus Treated with Oral Antidiabetic(s)
Type 2 Diabetes Mellitus
Phase 3
No
exenatide once weekly, insulin glargine
All
427
Interventional
20 Years +
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Verified 01 May 2015 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
Eli Lilly and Company
The objectives of this clinical trial are to compare the effects of exenatide once weekly and insulin glargine on blood glucose control, body weight, lipids, safety, and tolerability.
Arms | Assigned Interventions |
---|---|
Experimental: exenatide once weekly | Drug: exenatide once weekly subcutaneous injection, 2.0mg, once a week; |
Active Comparator: insulin glargine | Drug: insulin glargine subcutaneous injection, titrated to achieve fasting serum glucose target, once a day Other Name: insulin glargine-Lantus |
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