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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 mg and 400 mg total daily dose [TDD]) compared with placebo in adults with moderate to severe binge eating disorder (BED).

Clinical Trial Description


Study Design

Related Conditions & MeSH terms

NCT number NCT05113953
Study type Interventional
Source Otsuka Pharmaceutical Development & Commercialization, Inc.
Contact Otsuka Call Center
Phone 844-687-8522
Email [email protected]
Status Not yet recruiting
Phase Phase 2
Start date November 8, 2021
Completion date August 1, 2022

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