Johnson & Johnson Announces TREMFYA®'s Success in Inhibiting Joint Damage in Psoriatic Arthritis, Setting New Standards in IL-23 Inhibitor Efficacy

Reuters
06-11
Johnson & Johnson Announces TREMFYA®'s Success in Inhibiting Joint Damage in Psoriatic Arthritis, Setting New Standards in IL-23 Inhibitor Efficacy

Johnson & Johnson has announced findings from the Phase 3b APEX study demonstrating the efficacy of TREMFYA® (guselkumab) in treating active psoriatic arthritis. The study results, presented at the European Alliance of Associations for Rheumatology (EULAR) 2025 Congress, show that TREMFYA® significantly reduced signs and symptoms of the disease and inhibited the progression of joint structural damage at 24 weeks compared to placebo. More than 40% of patients treated with TREMFYA® achieved ACR50, a measure of improvement in joint symptoms, by Week 24. Additionally, a higher proportion of TREMFYA®-treated patients achieved clear or almost clear skin compared to those receiving placebo. The safety profile of TREMFYA® remains consistent with previous studies, with no new safety signals identified.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Johnson & Johnson published the original content used to generate this news brief via PR Newswire (Ref. ID: NY04448) on June 11, 2025, and is solely responsible for the information contained therein.

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