drugset / Trial / NCT02528409

Vortioxetine for Binge Eating Disorder

NCT02528409

Phase 2 Completed 80 enrolled University of Chicago Takeda · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The aim of the present study is to examine the efficacy and safety of vortioxetine vs placebo in adults with moderate to severe Binge eating disorder, as indicated by at least 3 binge eating days per week for the 2 weeks before the baseline visit.

Timeline

Start
2016-06
Primary completion
2018-11
Completion
2018-11-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Vortioxetine Unknown 20 mg

Indications