Clinical Trials · NCT01960179

Safety And Tolerability Of Lixisenatide In Monotherapy In Patients With Type 2 Diabetes

CompletedPhase 3Lixisenatide (Approved)
Phase
Phase 3
Recruitment status
Completed
Sponsor
Sanofi
Enrollment
361
Start date
Nov 2013
Locations
30 sites, Japan
Primary endpoint
Safety over 24 and 52 weeks assessed by treatment emergent adverse event (TEAE), vital signs, 12-lead electrocardiogram (ECG), and laboratory data.
View Lixisenatide compound reference