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Clinical Trial Summary

The primary objective of this study is to assess the efficacy of 2 doses of centanafadine sustained-release (SR) (200 milligrams [mg] and 400 mg total daily dose [TDD]) compared with placebo in adults with moderate to severe binge eating disorder (BED).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05113953
Study type Interventional
Source Otsuka Pharmaceutical Development & Commercialization, Inc.
Contact
Status Completed
Phase Phase 2
Start date December 16, 2021
Completion date August 30, 2022

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