Clinical Trial

A Study to Test the Effects of Centanafadine in Adults With Attention-deficit/Hyperactivity Disorder and Emotional Dysregulation

Not Yet Recruiting Phase 3
View on ClinicalTrials.gov →
Summary
The primary purpose of this study is to evaluate the efficacy of centanafadine once daily (QD) extended-release (XR) capsules in adults with attention-deficit/hyperactivity disorder (ADHD) and emotional dysregulation (ED).
Trial Details
NCT Number NCT07759154
Lead Sponsor Otsuka Pharmaceutical Development & Commercialization, Inc.
Conditions Attention-deficit/Hyperactivity Disorder, Emotional Dysregulation
Enrollment 80 participants
Start Date 2026-08-20
Primary Completion 2027-05-27 (estimated)
Study Completion 2027-05-27 (estimated)
Updated on ClinicalTrials.gov 2026-08-12