Tofacitinib in Adult Patients With Moderate to Severe Ulcerative Colitis
- Sponsor
- Pfizer
- Study ID
- NCT04424303
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Tofacitinib — DRUGObservational study
Study Details
This is an observational prospective study with two years of follow-up, designed to evaluate the effectiveness of tofacitinib in patients with moderate to severe ulcerative colitis in French clinical practice
Key Dates
- Start date
- Dec 4, 2020
- Status verified
- Jan 2026
- Primary completion
- Dec 8, 2025
- Completion
- Dec 8, 2025
Study Design
- Enrollment
- 152 participants (actual)
Arms
- Arm: Patients prescribed tofacitinibPatients with a confirmed diagnosis of moderate to severe ulcerative colitis initiating tofacitinib as per the French summary of product characteristics (SmPC).
Primary Outcome Measure
Proportion of patients with clinical benefit one year after initiation of tofacitinib treatment. [ Time Frame: Week 52 ]
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