​​​​​​​PsA Treatment Options Expand - Summary - MDSpire
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​​​​​​​PsA Treatment Options Expand

Phase 3 POETYK trial results support FDA approval of deucravacitinib for adults with active PsA.

  • By

  • Kathryn Wighton

  • March 9, 2026

  • 3 min

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Objective:

To report on the FDA approval of deucravacitinib for the treatment of adults with active psoriatic arthritis.

Approach:
    Key Findings:
    • Deucravacitinib achieved ACR20 response in 54% of patients in both trials compared to 34% and 39% in placebo groups.
    • ACR50 responses were 24% vs 14% and 29% vs 16% for deucravacitinib vs placebo in the two trials respectively.
    • ACR70 responses were 12% vs 5% and 10% vs 5% for deucravacitinib vs placebo.
    • Minimal disease activity was achieved by a greater proportion of patients receiving deucravacitinib.
    Interpretation:

    Deucravacitinib is the first TYK2 inhibitor approved for psoriatic arthritis, showing significant efficacy in improving disease activity compared to placebo.

    Limitations:
    • The trials included only adults aged 18 years or older with active PsA.
    • POETYK PsA-1 participants had not previously received biologic DMARDs, while POETYK PsA-2 included patients with prior TNF inhibitor exposure.
    Conclusion:

    Deucravacitinib represents a new therapeutic option for adults with active psoriatic arthritis, demonstrating improved outcomes in clinical trials.

    Sources:

Original Source(s)

​​​​​​​PsA Treatment Options Expand

  • by Kathryn Wighton

  • March 9, 2026

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