drugset / Trial / NCT02589626

Long-term Safety and Efficacy of Empagliflozin as Add on to GLP-1 RA

NCT02589626

Phase 4 Completed 65 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a multi-center, randomised, double-blind, parallel-group, safety and efficacy study of empagliflozin as add-on to GLP-1 RA in Japanese patients with Type 2 Diabetes Mellitus with insufficient glycaemic control

Timeline

Start
2015-10-29
Primary completion
2017-06-02
Completion
2017-06-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Empagliflozin Small molecule 10 mg
Subject Empagliflozin Small molecule 25 mg