drugset / Trial / NCT01620489

Efficacy and Safety of Liraglutide Versus Placebo as add-on to Existing Diabetes Medication in Subjects With Type 2 Diabetes and Moderate Renal Impairment

NCT01620489 ↗

Phase 3 Completed 279 enrolled Novo Nordisk A/S
RandomizedParallel-groupDouble-blindTreatment

Summary

This trial is conducted in Europe and the United States of America (USA). The aim of this trial is to investigate the efficacy and safety of liraglutide in subjects with type 2 diabetes and moderate renal impairment. The trial medication will be add-on to the subject's stable pre-trial OAD and/or insulin regimen.

Timeline

Start
2012-06-14
Primary completion
2013-08-20
Completion
2013-08-20

Outcome

Met primary endpoint

registry analysis (superiority or other test); Lira 1.8 mg vs Placebo; p <0.0001; Estimated treatment difference -0.66 (95% CI -0.90 to -0.43); Mixed Models Analysis NCT01620489 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Liraglutide Peptide 1.8 mg Subcutaneous