LivingGLP1
Study S001455

A 13-week Multinational, Randomized, Double-Blind, Placebo-Controlled, Dose-Response Trial Assessing the Safety, Tolerability and Efficacy of AVE0010 in Metformin-Treated Subjects With Type 2 Diabetes Mellitus

Registration

Registration
NCT00299871
Study type
INTERVENTIONAL
Allocation
RANDOMIZED
Phase
PHASE2
Masking
DOUBLE
Status
COMPLETED
Enrollment
542
Start
2006-02
Primary completion
2007-08
Lead sponsor
Sanofi
Conditions
Type 2 Diabetes
Interventions
DRUG:LIXISENATIDE (AVE0010)
Results posted
FALSE

Registered primary outcomes

  • HbA1c levels at baseline and endpoint (at 13 weeks). []

Linked records (1)

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
R0021613Dose-dependent effects of the once-daily GLP-1 receptor agonist lixisenatide in patients with Type 2 diabetes inadequately controlled with metformin: a randomized, double-blind, placebo-controlled trial.
Ratner RE, Diabetic medicine : a journal of the British Diabetic Association
2010Randomized trialPMID 20722676DOIregistry reference RESULT:20722676