drugset / Trial / NCT00294723

To Evaluate the Effect of Liraglutide Versus Glimepiride (Amaryl®) on Haemoglobin A1c

NCT00294723 ↗

Phase 3 Terminated 746 enrolled Novo Nordisk A/S
RandomizedParallel-groupDouble-blindTreatment

Summary

This trial is conducted in North America (the United States of America (USA) and Mexico). The trial is designed to evaluate the effects of treatment with liraglutide versus glimepiride in subjects with type 2 diabetes. The trial is a 52-week randomised, double-blind trial period plus a 52-week open-label extension (week 104) followed by an additional 156-week continued open-label extension. The total duration of the treatment period is planned to be 260 weeks (5 years).

Timeline

Start
2006-02
Primary completion
2008-11
Completion
2008-11

Outcome

Met primary endpoint

Stopped: “The trial was terminated at week 195 due to an insufficient number of subjects remaining to obtain reasonable statistical power”

registry analysis (non-inferiority or equivalence test); Lira 1.8 vs Glimepiride; p <0.0001; Estimated treatment difference, LS Mean -0.62 (95% CI -0.83 to -0.42) NCT00294723 ↗

registry analysis (non-inferiority or equivalence test); Lira 1.8 vs Glimepiride; p <.0001; Estimated treatment difference, LS Mean -0.60 (95% CI -0.83 to -0.38) NCT00294723 ↗

registry analysis (non-inferiority or equivalence test); Lira 1.8 vs Glimepiride; p <0.0001; Estimated treatment difference, LS Mean -0.55 (95% CI -0.77 to -0.34) NCT00294723 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Glimepiride Small molecule 8 mg —
Subject Liraglutide Peptide 1.2 mg Subcutaneous
Subject Liraglutide Peptide 1.8 mg Subcutaneous