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A Study to Determine the Efficacy and Safety of Deucravacitinib Compared With Placebo in Participants With Active Psoriatic Arthritis (PsA) Who Are Naïve to Biologic Disease Modifying Anti-rheumatic Drugs or Had Previously Received TNFα Inhibitor Treatment

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NCT04908189 · results posted

Sponsored by Bristol-Myers Squibb (industry) · BMY — their whole pipeline →.

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
729actual
Sites
138
Countries
Argentina, Australia, Belgium +15

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
DateFiledBasisWhat it is
Start2021-07-15actualWhen the study began enrolling
Primary completion2024-02-06actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-11-12estimatedThe whole study's end, after follow-up
First posted2021-06-01actualWhen this record first appeared on the registry
Results posted2025-04-13actualWhen the sponsor posted results to the registry
Record updated2025-06-13actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Psoriatic Arthritis

Interventions

  • Drug: Deucravacitinib — also filed as BMS-986165
  • Other: Placebo
  • Drug: Apremilast — also filed as Otezla

Primary outcome

what the primary-completion date above is the date OF
Number of Participants Meeting American College of Rheumatology (ACR) 20 at Week 16
measured Week 16

Posted documents

hosted by the registry — we link, never re-serve
Study Protocol and Statistical Analysis Planposted 2022-03-20 · 7.7 MB · Prot_SAP_000.pdf

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