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International news: secukinumab approved as a treatment option for patients aged 12 and older

This article reflects information published on March 29, 2026.

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HS does not affect adults alone

1. Overview

In March 2026, the IL-17A inhibitor secukinumab (Cosentyx) was approved by the US FDA for HS in patients aged 12 and older, extending treatment options beyond adults to younger patients.

2. Key points

Where US Food and Drug Administration (FDA); Novartis announcement, March 2026

Subject IL-17A inhibitor Secukinumab for moderate to severe HS: Expanded indication for patients aged 12 and older

Key points HS treatments have largely focused on adults. This approval

  • extends treatment options to children and adolescents.
  • Weight-based dosing
  • Assessment based on adult and pediatric data

These are among the features described in the announcement.

This may reflect growing recognition in medical care that HS does not affect adults alone.

3. HSVCJ's perspective

HS symptoms often begin around puberty. However, HS is not always diagnosed at that stage, and I feel that many people live with what they regard as recurring boils.

Discussion of treatments for younger people may encourage appropriate care at an earlier stage.

Treatment choices depend on individual circumstances, and no treatment is appropriate for everyone.

We will continue to follow this development and changes in how HS is understood.

4. Sources

Official Novartis announcement https://www.novartis.com/news/media-releases/novartis-cosentyx-receives-fda-approval-pediatric-patients-aged-12-moderate-severe-hidradenitis-suppurativa

Coverage of FDA approval https://www.ajmc.com/view/fda-expands-secukinumab-approval-to-patients-12-years-and-older-with-hidradenitis-suppurativa

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