Spondyloarthritis & psoriatic arthritis

Efficacy and safety of deucravacitinib, an oral, selective tyrosine kinase 2 inhibitor, in patients with active psoriatic arthritis: 52-week results from the randomised, double-blind, placebo-controlled phase 3 POETYK PsA-1 trial

Ann Rheum DisPublished Randomised controlled trial

Authors' conclusion

Deucravacitinib demonstrated superiority vs placebo for clinical responses, patient-reported outcomes, and structural damage inhibition in patients with PsA, with favourable tolerability and safety.

Study context

Population
Adults with active PsA naïve to bDMARDs, high-sensitivity CRP ≥ 3 mg/L and ≥ 1 PsA-related hand and/or foot erosion on radiograph
Participants
670 adults
Comparison
Deucravacitinib 6 mg orally once daily vs placebo through W16, then all on deucravacitinib through W52
Primary endpoint
ACR20 response
Follow-up
W16
Methodological detailsdouble-blind, placebo-controlled, phase 3
  • Double-blind
  • Placebo-controlled
  • Phase 3

Primary result

As reported in the abstract

ACR20

P < 0.001

Further findings

Responses with deucravacitinib · W52

Responses with deucravacitinib were increased at W52; placebo-to-deucravacitinib switchers achieved improvements similar to continuous deucravacitinib

Structural damage · W16 and W52

Inhibition of structural damage observed at W16 and W52
  • Post hoc rank analysis of covariance, no missing data imputation

Deaths

No deaths occurred
No imbalances in cardiovascular events, malignancies, or opportunistic infections; no new safety signals

Safety

Serious AEs · W16

Discontinuations due to AEs · W16

  • Serious adverse events (AEs): remained low through W52
  • Discontinuations due to AEs: remained low through W52

Original publication

Efficacy and safety of deucravacitinib, an oral, selective tyrosine kinase 2 inhibitor, in patients with active psoriatic arthritis: 52-week results from the randomised, double-blind, placebo-controlled phase 3 POETYK PsA-1 trial. Ann Rheum Dis. Published 7 August 2026. doi:10.1016/j.ard.2026.05.029

Composed by AI from the published abstract and checked against it. How Briefs are made →

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