LivingGLP1
Study S001599

An Open-label, Multicenter 24-Week And 52-Week Study Assessing The Safety And Tolerability Of Lixisenatide In Monotherapy In Patients With Type 2 Diabetes

Registration

Registration
NCT01960179
Study type
INTERVENTIONAL
Phase
PHASE3
Masking
NONE
Status
COMPLETED
Enrollment
361
Start
2013-11
Primary completion
2015-03
Lead sponsor
Sanofi
Conditions
Type 2 Diabetes Mellitus
Interventions
DRUG:lixisenatide AVE0010
Results posted
FALSE
Secondary identifiers
OTHER:U1111-1134-2695

Registered primary outcomes

  • Safety over 24 and 52 weeks assessed by treatment emergent adverse event (TEAE), vital signs, 12-lead electrocardiogram (ECG), and laboratory data. [from baseline to 24 weeks and 52 weeks]

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