Skip to content

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

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

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2080223189
Enrollment
200
Registered
2016-05-09
Start date
2016-05-12
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Attention-Deficit/Hyperactivity Disorder (ADHD)

Interventions

Sponsors

Taisho Pharmaceutical co., LTD
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Child patients diagnosed with ADHD - Outpatients etc.

Exclusion criteria

Exclusion criteria: - Having other central nervous system disease etc.

Design outcomes

Primary

MeasureTime frame
efficacy efficacy(frequency of ADHD)

Secondary

MeasureTime frame
efficacy efficacy(degree of ADHD,QOL etc)

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026