Clinical Trials · NCT01572649

Evaluation of the Blood Levels of the Drug (Lixisenatide), the Plasma Glucose Levels and Safety in Paediatric and Adult Patients With Type 2 Diabetes

CompletedPhase 1Lixisenatide (Approved)
Phase
Phase 1
Recruitment status
Completed
Sponsor
Sanofi
Enrollment
24
Start date
May 2012
Locations
6 sites, 4 countries
Primary endpoint
GLU-AUC 0:30-4:30h: area under the plasma glucose concentration time profile from time of the standardized breakfast start (30 min after IMP injection and pre-meal plasma glucose) until 4 hours later subtracting the pre-meal value
View Lixisenatide compound reference