drugset / Trial / NCT01140906

Randomised Placebo-controlled Duloxetine-referenced Study of Efficacy and Safety of 15 and 20 mg of Vortioxetine (Lu AA21004) in Acute Treatment of Major Depressive Disorder in Adults

NCT01140906 ↗

Phase 3 Completed 607 enrolled H. Lundbeck A/S
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of the study is to evaluate the efficacy, tolerability and the safety of two fixed doses of vortioxetine in the treatment of major depressive disorder.

Timeline

Start
2010-05
Primary completion
2011-09
Completion
—

Outcome

Met primary endpoint

registry Placebo vs Vortioxetine 15 mg; p <0.0001; Mean Difference (Final Values) -5.53 (95% CI -7.66 to -3.40) NCT01140906 ↗

registry Placebo vs Vortioxetine 20 mg; p <0.0001; Mean Difference (Final Values) -7.09 (95% CI -9.21 to -4.97) NCT01140906 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Duloxetine Small molecule 60 mg Oral
Subject Vortioxetine Unknown 15 mg Oral
Subject Vortioxetine Unknown 20 mg Oral