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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


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

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