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Phase2 Study of TS-141 in Child Patients With ADHD (Double-blind, Parallel Group Study)

Phase 2
Completed
Conditions
Attention-Deficit/Hyperactivity Disorder (ADHD)
Registration Number
JPRN-jRCT2080223189
Lead Sponsor
Taisho Pharmaceutical co., LTD
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
completed
Sex
All
Target Recruitment
200
Inclusion Criteria

Child patients diagnosed with ADHD
- Outpatients
etc.

Exclusion Criteria

- Having other central nervous system disease
etc.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
efficacy<br>efficacy(frequency of ADHD)
Secondary Outcome Measures
NameTimeMethod
efficacy<br>efficacy(degree of ADHD,QOL etc)
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