Novartis Cosentyx® receives FDA approval for pediatric patients aged 12+ with moderate to severe hidradenitis suppurativa [Yahoo! Finance]
Novartis AG (NVS)
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Source: Yahoo! Finance
Novartis Pharma AG Cosentyx is the only IL-17A inhibitor approved for this population, and the first differentiated mechanism in nearly a decade HS often emerges around puberty, underscoring importance of early diagnosis and intervention with biologics to help reduce long-term disease burden Approval marks fourth pediatric indication for Cosentyx, reinforcing its robust safety and efficacy profile Basel, March 13, 2026 – Novartis announced today that Cosentyx ® (secukinumab) received US Food and Drug Administration (FDA) approval for treating pediatric patients 12 years and older with moderate to severe hidradenitis suppurativa (HS), making it the only IL-17A inhibitor for this population . The approval of a distinct biologic option for pediatric patients living with HS allows treatment to be tailored to the individual and establishes Cosentyx as a meaningful addition to the treatment landscape “Hidradenitis suppurativa (HS) often begins in adolescence and can cause irrever
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