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Novartis Cosentyx® receives FDA approval for pediatric patients aged 12+ with moderate to severe hidradenitis suppurativa

Cosentyx is the only IL-17A inhibitor approved for this population, and the first differentiated mechanism in nearly a decade1-3 HS often emerges around puberty, underscoring importance of early diagnosis and intervention with biologics to help reduce long-term disease burden4-6 Approval marks fourth pediatric indication for Cosentyx, reinforcing its robust safety and efficacy profile1 Basel, March 13, 2026 – Novartis announced today that Cosentyx® (secukinumab) received US Food and Drug Adminis

articleNovartis AgMarch 13, 202610/company/novartis-ag/news/novartis-cosentyxr-receives-fda-approval-for-pediatric-patients-aged-12-with-moderate-to-severe-hidradenitis-suppurativa
Novartis Cosentyx® receives FDA approval for pediatric patients aged 12+ with moderate to severe hidradenitis suppurativa

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hidradenitis suppurativaFDACosentyxNovartispsoriatic arthritispediatric patientstreatment optionstreatment option