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
This is a phase 3 trial designed to compare the effects of twice daily exenatide plus oral antidiabetic agents (OADs) and once-daily insulin glargine plus OADs with respect to glycemic control, as measured by hemoglobin A1c, with minimum weight gain, in patients with uncontrolled type 2 diabetes on OADs.
Location
Location
London, United Kingdom
Location
Torquay, United Kingdom
Location
Wakefield, United Kingdom
Location
Swansea, United Kingdom
Location
Oldham, United Kingdom
Location
Nottingham, United Kingdom
Location
High Wycombe, United Kingdom
Location
Liverpool, United Kingdom
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 |
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