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Rhapsido FDA Approval History

FDA Approved: Yes (First approved September 30, 2025)
Brand name: Rhapsido
Generic name: remibrutinib
Dosage form: Tablets
Company: Novartis Pharmaceuticals Corporation
Treatment for: Urticaria

Rhapsido (remibrutinib) is a kinase inhibitor indicated for the treatment of chronic spontaneous urticaria (CSU) in adult patients who remain symptomatic despite H1 antihistamine treatment.

Development timeline for Rhapsido

DateArticle
Sep 30, 2025Approval FDA Approves Rhapsido (remibrutinib) for the Treatment of Chronic Spontaneous Urticaria

Further information

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