A Real-world Observational Study to Compare Effectiveness of Deucravacitinib Vs Apremilast in Adults With Plaque Psoriasis
← catalyst calendarNCT05744466 · readout in 478 d
Sponsored by Bristol-Myers Squibb (industry) · BMY — their whole pipeline →.
Phase
—
Status
Recruiting
Study type
Observational
Enrollment
1,500estimated
Sites
1
Country
United States
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
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2022-09-30 | actual | When the study began enrolling |
| Primary completion | 2027-12-10 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2027-12-10 | estimated | The whole study's end, after follow-up |
| First posted | 2023-02-27 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2024-07-23 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Psoriasis
Interventions
- Drug: Deucravacitinib
- Drug: Apremilast
Primary outcomes
what the primary-completion date above is the date OFChange in body surface area (BSA)
measured At baseline and every 6 months up to 60 months or treatment discontinuation
Investigator global assessment (IGA) response 0/1
measured Up to 60 months
Dermatology life quality index (DLQI) response 0/1
measured Up to 60 months
Time from date of treatment initiation to date of discontinuation
measured Up to 60 months
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