All content on this site is intended for healthcare professionals only. By acknowledging this message and accessing the information on this website you are confirming that you are a Healthcare Professional.

  TRANSLATE

The pso Hub website uses a third-party service provided by Google that dynamically translates web content. Translations are machine generated, so may not be an exact or complete translation, and the pso Hub cannot guarantee the accuracy of translated content. The pso and its employees will not be liable for any direct, indirect, or consequential damages (even if foreseeable) resulting from use of the Google Translate feature. For further support with Google Translate, visit Google Translate Help.

The PsOPsA Hub is an independent medical education platform, supported by educational grants. We would like to express our gratitude to the following companies for their support: UCB, for website development, launch, and ongoing maintenance; UCB, for educational content and news updates. The funders are allowed no direct influence on our content. The levels of sponsorship listed are reflective of the amount of funding given.  

Now you can support HCPs in making informed decisions for their patients

Your contribution helps us continuously deliver expertly curated content to HCPs worldwide. You will also have the opportunity to make a content suggestion for consideration and receive updates on the impact contributions are making to our content.

Find out more

POETYK phase III trials: Pooled analyses of deucravacitinib in psoriatic arthritis

By Sheetal Bhurke

Share:

Dec 3, 2025

Learning objective: After reading this article, learners will be able to cite a new clinical development in psoriatic arthritis.


During the American College of Rheumatology (ACR) Convergence 2025, October 24–29, 2025, Chicago, US, Atul Deodhar presented findings from the pooled analyses of the pivotal phase III POETYK PsA-1 (NCT04908202) and PsA-2 (NCT04908189) trials, evaluating the efficacy of deucravacitinib, a first-in-class, oral tyrosine kinase 2 (TYK2) inhibitor, vs placebo in adult patients with psoriatic arthritis (PsA) (N = 1,294). Patients were randomized to deucravacitinib 6 mg once daily (n = 648) or placebo (n = 646) for 16 weeks. This analysis assessed composite measures of disease activity, including minimal disease activity (MDA), Disease Activity in Psoriatic Arthritis (DAPSA), Psoriatic Arthritis Response Criteria (PsARC), and Psoriatic Arthritis Disease Activity Score (PASDAS).

Key data: At Week 16, a higher proportion of patients treated with deucravacitinib compared with placebo achieved MDA response (PsA-1, p = 0.0012; PsA-2, p = 0.0007; pooled, p < 0.0001), DAPSA low disease activity or remission (PsA-1, p = 0.0001; PsA-2, p < 0.0001; pooled, p < 0.0001), DAPSA disease remission (PsA-1, p = 0.0009; PsA-2, p = 0.0005; pooled, p < 0.0001), PsARC response (PsA-1, p < 0.0001; PsA-2, p < 0.0001; pooled, p < 0.0001), and PASDAS (PsA-1, p < 0.0001; PsA-2, p < 0.0001; pooled, p < 0.0001).

Key learning: Deucravacitinib demonstrated improvements in global disease activity compared with placebo in patients with PsA, supporting the primary results of the POETYK PsA trials.

References

Please indicate your level of agreement with the following statements:

The content was clear and easy to understand

The content addressed the learning objectives

The content was relevant to my practice

I will change my clinical practice as a result of this content