drugset / Trial / NCT01960179
Safety And Tolerability Of Lixisenatide In Monotherapy In Patients With Type 2 Diabetes
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Lixisenatide | Peptide | — | Subcutaneous |