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Drug Use-results survey for Simponi 50mg

Drug Use-results survey for Simponi 50mg - Drug Use-results survey for Simponi 50mg

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000015895
Enrollment
3000
Registered
2014-12-15
Start date
2011-09-16
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

Rheumatoid Arthritis

Interventions

None listed

Sponsors

Janssen Pharmaceutical K.K.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with rheumatoid arthritis who are treated with Simponi

Exclusion criteria

Exclusion criteria: NA

Design outcomes

Primary

MeasureTime frame
Safety (Adverse Drug Reaction) Effectiveness (Disease Activity Score 28, Visual Analog Scale)

Countries

Japan

Contacts

Public ContactAkiko Yamamoto

Janssen Pharmaceutical K.K. Safety Risk Management Dept.

ayamamot@its.jnj.com03-4411-5173

Outcome results

None listed

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