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2024-11-12T13:53:42.000Z

Achievement of MDA with deucravacitinib in PsA: Results from a phase II trial

Nov 12, 2024
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Learning objective: After reading this article, learners will be able to cite a new clinical development in psoriatic arthritis.


Deucravacitinib is a novel TYK2 inhibitor that is approved for the treatment of psoriasis in multiple countries and is currently being investigated in PsA. A phase II, multicenter, double-blind trial (NCT03881059) evaluated the safety and efficacy of deucravacitinib in PsA. Patients were randomized 1:1:1 to deucravacitinib (6 mg or 12 mg) or placebo. A post-hoc analysis of this trial, published in Oxford Rheumatology, evaluated the achievement of MDA components through Week 16. Achievement of MDA is associated with improved outcomes and quality of life in patients with PsA.


Key learnings
Deucravacitinib was more effective than placebo in achieving MDA after 16 weeks, with 22.9% and 23.9% of patients treated with 6 mg and 12 mg deucravacitinib meeting MDA criteria compared with 7.6% of patients treated with placebo.
Deucravacitinib-treated patients showed improvement across MDA components, such as tender/swollen joint counts, patient-reported pain, and skin psoriasis (PASI score). All MDA responders met the tender entheseal points ≤1 criterion; however, 47.3% of patients had already met the criterion at baseline.
Improvements in several MDA components, including physical functioning and pain, were evident as early as 4 weeks after treatment initiation, indicating a rapid onset of action.
These findings suggest that deucravacitinib could be a viable alternative for patients who cannot achieve adequate disease control with existing PsA therapies, potentially improving both short- and long-term quality of life and function in these patients.

Abbreviations: MDA, minimal disease activity; PASI, psoriasis area and severity index; PsA, psoriatic arthritis. 

  1. Kavanaugh A, Coates LC, Mease PJ, et al. Deucravacitinib, a selective, TYK2 inhibitor, in psoriatic arthritis: Achievement of minimal disease activity components in a phase 2 trial. Rheumatology (Oxford). Online ahead of print. DOI: 10.1093/rheumatology/keae580

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