Clinical Trial

A Trial to Evaluate the Efficacy and Safety of EB-1020 in Pediatric Patients With ADHD

Recruiting Phase 2/3
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Summary
The purpose of this study is to evaluate the efficacy and examine the safety of two doses of EB-1020 QD XR capsule administered once daily orally in pediatric ADHD patients.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-07-17.
Trial Details
NCT Number NCT07086313
Lead Sponsor Otsuka Pharmaceutical Co., Ltd.
Conditions Attention-Deficit Hyperactivity Disorder(ADHD)
Enrollment 315 participants
Start Date 2025-09-03
Primary Completion 2027-08 (estimated)
Study Completion 2027-08 (estimated)
Updated on ClinicalTrials.gov 2025-12-23