Dasotraline Binge Eating Disorder Study

Status Completed

Clinical Trial Summary

Evaluate the efficacy of flexibly-dosed dasotraline compared with placebo in adults with moderate to severe Binge Eating Disorder (BED)

Clinical Trial Description

This is a randomized, double blind, parallel group, multicenter, outpatient study evaluating the efficacy and safety of flexibly-dosed dasotraline in adults with BED using dasotraline (4, 6, and 8 mg/day) versus placebo over a 12 week treatment period. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02564588
Study type	Interventional
Source	Sunovion
Contact
Status	Completed
Phase	Phase 2/Phase 3
Start date	October 2015
Completion date	October 2016

View Details

See also
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