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Special Drug Use-results survey for long-term administration of Stelara

Special Drug Use-results survey for long-term administration of Stelara - Special Drug Use-results survey for long-term administration of Stelara

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000015899
Enrollment
1500
Registered
2014-12-15
Start date
2011-03-14
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

psoriasis vulgaris, psoriatic arthritis

Interventions

None listed

Sponsors

Janssen Pharmaceutical K.K.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: patients with psoriasis vulgaris or psoriatic arthritis who do not have adequate response to conventional treatments in actual medical practice

Exclusion criteria

Exclusion criteria: NA

Design outcomes

Primary

MeasureTime frame
Safety(Adverse Drug Reaction) Effectiveness(Psoriasis Area and Severity Index(PASI))

Countries

Japan

Contacts

Public ContactYuko Kojima

Janssen Pharmaceutical K.K. Safety Risk Management Dept.

ykojima4@its.jnj.com03-4411-5437

Outcome results

None listed

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