Secukinumab Trial Targets Relapsed Polymyalgia Rheumatica
MDSpire News
July 31, 2026
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In the REPLENISH trial, 41% of patients receiving secukinumab achieved sustained remission at 52 weeks compared to 20% receiving placebo.
The trial enrolled 381 patients aged 50 or older with relapsed polymyalgia rheumatica across 148 sites in 28 countries.
Complete sustained remission occurred in 28% of the secukinumab 300 mg group, 25% in the 150 mg group, and 5% in the placebo group.
Patients receiving secukinumab had lower annual cumulative glucocorticoid exposure, with doses 20% to 23% lower than the placebo group.
Serious adverse events occurred in 14-16% of patients in the secukinumab groups, with fungal infections reported more frequently than in the placebo group.
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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