← Back

Wire · operational-macro

US FDA expands use of Novartis drug for chronic skin condition

Published

7 October 2026

Topic

operational-macro

◆ Sectors

Health

◆ Geography

United States

◆ Source

Read at reuters.com →

◆ Verified

Fusion42 · 11 October 2026 · Fusion42 review

The US FDA has expanded the approved use of Novartis' drug remibrutinib (Rhapsido) to treat symptomatic dermographism in adults, a chronic skin condition with itchy welts triggered by scratching or friction. This approval follows positive late-stage trial results showing significant symptom resolution and expands remibrutinib's treatment scope beyond chronic spontaneous urticaria.

This Wire brief sits within Fusion42's coverage of Health, and 7 sources have reported it between 7 Oct 2026 and 10 Oct 2026.

◆ ◆ The Wire takeaway

Novartis' expanded FDA approval opens new patient markets for remibrutinib, signalling an opportunity for drug developers focusing on chronic skin conditions to accelerate product outreach and partnerships in the US.

◆ Coverage

7 sources · first reported 7 Oct 2026 · latest 10 Oct 2026

◆ Topics

Healthfda-approvalnovartischronic-skin-conditionpharma-regulationremibrutinib