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Specified drug use results survey of Stelara in patients with ulcerative colitis

Specified drug use results survey of Stelara in patients with ulcerative colitis - Specified drug use results survey of Stelara in patients with ulcerative colitis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000051601
Enrollment
300
Registered
2023-07-15
Start date
2020-09-30
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

ulcerative colitis

Interventions

None listed

Sponsors

Janssen Pharmaceutical K.K.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who initiate Stelara for moderate to severe active ulcerative colitis(Only patients who have failed or were intolerant to previous treatment)

Exclusion criteria

Exclusion criteria: Patients with a history of the use of ustekinumab(active ingredient of this product)

Design outcomes

Primary

MeasureTime frame
Safety(ADR) Effectiveness(Partial Mayo Score)

Countries

Japan

Contacts

Public ContactMasayuki Takagishi

Janssen Pharmaceutical K.K. Safety Science and Risk Management Dept.

mtakagis@its.jnj.com03-4411-5136

Outcome results

None listed

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