A Study to Evaluate Deucravacitinib in Participants With Moderate-to-Severe Plaque Psoriasis in Germany
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Phase
—
Status
Active, not recruiting
Study type
Observational
Enrollment
550estimated
Sites
2
Country
Germany
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 | 2023-04-13 | actual | When the study began enrolling |
| Primary completion | 2025-08-18 | actual | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2030-05-31 | estimated | The whole study's end, after follow-up |
| First posted | 2023-10-27 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2025-12-04 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Plaque Psoriasis
Intervention
- Drug: Deucravacitinib
Primary outcome
what the primary-completion date above is the date OFProportion of patients achieving an absolute Psoriasis Area Severity Index (aPASI) score ≤ 3 at Week 24 or nearest visit
measured Approximately 24 weeks after treatment initiation (data to be collected at visit nearest to this timepoint)
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