FDA approves tildrakizumab for psoriatic arthritis
MDSpire News
October 30, 2026
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The FDA approved tildrakizumab-asmn for adults with active psoriatic arthritis, expanding its use beyond moderate-to-severe plaque psoriasis.
The approval was supported by INSPIRE-1 and INSPIRE-2, phase 3 trials of tildrakizumab 100 mg in adults with active psoriatic arthritis.
In a pooled analysis of 806 participants, week 24 ACR20 responses occurred in 38.8% of patients receiving tildrakizumab and 24.4% receiving placebo.
Among participants with psoriasis affecting at least 3% of body surface area, 41.0% receiving tildrakizumab and 10.9% receiving placebo achieved at least 75% PASI improvement.
The most common adverse reactions, each reported in at least 3% of patients with psoriatic arthritis, were upper respiratory tract infections and COVID-19.
This content is an AI-generated, fully rewritten summary based on a published scholarly article. It does not reproduce the original text and is not a substitute for the original publication. Readers are encouraged to consult the source for full context, data, and methodology.
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