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Special Drug Use-results Survey for Long-term Administration of Invega 3mg/6mg/9mg Tablet

Special Drug Use-results Survey for Long-term Administration of Invega 3mg/6mg/9mg Tablet - Special Drug Use-results Survey for Long-term Administration of Invega 3mg/6mg/9mg Tablet

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000015599
Enrollment
1350
Registered
2014-11-07
Start date
2011-01-17
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

Schizophrenia

Interventions

None listed

Sponsors

Janssen Pharmaceutical K.K.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with schizophrenia who are treated with Invega Tablet for the first time

Exclusion criteria

Exclusion criteria: NA

Design outcomes

Primary

MeasureTime frame
Sefety(Adverse Drug Reaction) Effectiveness(Clinical Global Impression-Schizophrenia)

Secondary

MeasureTime frame
Effectiveness(Social and Occupational Functioning Assessment Scale)

Countries

Japan

Contacts

Public ContactKeiko Imai

Janssen Pharmaceutical K.K. Safety Risk Management Dept.

kimai4@ITS.JNJ.com03-4411-5752

Outcome results

None listed

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