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Comparison of Vortioxetine and Desvenlafaxine in Adult Patients Suffering From Depression — VIVRE  

Major Depressive Disorder Clinical Trial

Official title:
A Randomised, Double-blind, Parallel-group, Active Controlled Study Evaluating the Efficacy of Vortioxetine Versus Desvenlafaxine in Adult Patients Suffering From Major Depressive Disorder With Partial Response to SSRI Treatment

Clinical Trial 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

Clinical Trial Description

The study will consist of a screening period of up to 14 days before the Baseline Visit, followed by an 8-week Treatment Period with vortioxetine or desvenlafaxine. A Safety Follow-up Visit will be performed approximately 4 weeks after the Primary Outcome/Withdrawal Visit. At Baseline, patients will be equally randomised (1:1) to 1 of the 2 treatment groups for an 8-week, double-blind Treatment Period. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04448431
Study type Interventional
Source H. Lundbeck A/S
Contact
Status Completed
Phase Phase 4
Start date June 18, 2020
Completion date February 4, 2022
View Details
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