A Study to Evaluate Efficacy and Long-term Safety of Oral Ozanimod in Chinese Participants With Moderately to Severely Active Ulcerative Colitis (UC)
← catalyst calendarSponsored by Bristol-Myers Squibb (industry) · BMY — their whole pipeline →.
Phase
Phase 3
Status
Terminated
Study type
Interventional
Design
Randomized · Triple · Treatment
Enrollment
131actual
Sites
51
Countries
China, Taiwan
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-08-19
Why the sponsor stopped it
Business objectives have changed
As filed on the registry record, in the sponsor's own words.
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2022-12-09 | actual | When the study began enrolling |
| Primary completion | 2025-03-07 | actual | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2025-03-07 | actual | The whole study's end, after follow-up |
| First posted | 2022-12-09 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2025-03-26 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Ulcerative Colitis
Interventions
- Drug: Ozanimod — also filed as BMS-986374
- Drug: Placebo
Primary outcome
what the primary-completion date above is the date OFProportion of participants with clinical remission as measured by the 3-component Mayo Score
measured At week 10
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