LivingGLP1
Study S001323

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

Registration

Registration
NCT00360334
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE3
Masking
NONE
Status
COMPLETED
Enrollment
235
Start
2006-06
Primary completion
2008-04
Lead sponsor
AstraZeneca
Conditions
Type 2 Diabetes
Interventions
DRUG:exenatide; DRUG:insulin glargine
Results posted
TRUE

Registered primary outcomes

  • Percent of Patients Who Achieved HbA1c ≤ 7.4% With Minimal Weight Gain (≤ 1kg) [26 weeks]

Linked records (2)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R0018919Exenatide twice daily: analysis of effectiveness and safety data stratified by age, sex, race, duration of diabetes, and body mass index.
Pencek R, Postgraduate medicine
2012Randomized trialPMID 22913891DOIcites ClinicalTrials.gov:NCT00360334; registry reference DERIVED:22913891
R0024925Exenatide compared with long-acting insulin to achieve glycaemic control with minimal weight gain in patients with type 2 diabetes: results of the Helping Evaluate Exenatide in patients with diabetes compared with Long-Acting insulin (HEELA) study.
Davies MJ, Diabetes, obesity & metabolism
2009Randomized trialPMID 19930005DOIregistry reference RESULT:19930005