drugset / Trial / NCT04448431

Comparison of Vortioxetine and Desvenlafaxine in Adult Patients Suffering From Depression

NCT04448431 ↗

Phase 4 Completed 605 enrolled H. Lundbeck A/S
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to compare the efficacy of vortioxetine versus desvenlafaxine after 8 weeks of treatment in patients that have tried one available treatment without getting the full benefit

Timeline

Start
2020-06-18
Primary completion
2022-01-06
Completion
2022-02-04

Outcome

Met primary endpoint

paper Non-inferiority of vortioxetine versus desvenlafaxine was established in terms of mean change from baseline to week 8 in MADRS total score PMID 37227402 ↗

Drugs

EvaluationDrugModalityDoseRoute
Comparator Desvenlafaxine Other / unclassified 50 mg Oral
Subject Vortioxetine Unknown 10 mg Oral
Subject Vortioxetine Unknown 20 mg Oral