A Study to Evaluate the Utilization, Effectiveness, and Quality of Life of Ozanimod in Participants With Ulcerative Colitis
NCT05382715 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 175
Last updated 2025-07-02
Summary
The purpose of this study is to monitor the use, effectiveness and treatment persistence with Ozanimod (Zeposia®) as well as quality of life in participants undergoing treatment for moderate-to-severe ulcerative colitis (UC).
Conditions
- Colitis, Ulcerative
Interventions
- DRUG
-
Ozanimod
Specified Dose on Specified Days
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Bristol-Myers Squibb · Bristol-Myers Squibb
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-05-30
- Primary Completion
- 2025-05-31
- Completion
- 2025-05-31
- FDA Drug
- Yes
Countries
- Germany
Study Locations
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