drugset / Trial / NCT01960179

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

NCT01960179

Phase 3 Completed 361 enrolled Sanofi
NaSingle-groupOpen-labelTreatment

Summary

Primary Objective: To assess the overall safety of lixisenatide once daily treatment in monotherapy over 24 and 52 weeks in patients with type 2 diabetes in Japan Secondary Objective: To assess the effects of lixisenatide once daily treatment in monotherapy over 24 and 52 weeks on: * HbA1c (Glycated hemoglobin A1c) reduction; * Fasting plasma glucose; * Body weight.

Timeline

Start
2013-11
Primary completion
2015-03
Completion
2015-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Lixisenatide Peptide Subcutaneous