Evaluation of the Efficacy and Safety of EB-1020 in Adult ADHD Patients

PHASE2/PHASE3RecruitingINTERVENTIONAL
Enrollment

630

Participants

Timeline

Start Date

April 30, 2025

Primary Completion Date

December 31, 2027

Study Completion Date

December 31, 2027

Conditions
Attention Deficit Hyperactivity Disorder (ADHD)
Interventions
DRUG

EB-1020 (Centanafadine) 164.4 mg

164.4 mg, capsule, oral, once daily, for 6 weeks

DRUG

EB-1020 (Centanafadine) 328.8 mg

328.8 mg, capsule, oral, once daily, for 6 weeks

DRUG

Placebo

Placebo, capsule, oral, once daily, for 6 weeks

Trial Locations (1)

Unknown

RECRUITING

Maynds Tower Mental Clinic, Tokyo

All Listed Sponsors
lead

Otsuka Pharmaceutical Co., Ltd.

INDUSTRY

NCT06931080 - Evaluation of the Efficacy and Safety of EB-1020 in Adult ADHD Patients | Biotech Hunter | Biotech Hunter