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Novartis wins EU approval for Rhapsido in chronic spontaneous urticaria
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Novartis wins EU approval for Rhapsido in chronic spontaneous urticaria
  • European Commission cleared Novartis oral BTK inhibitor Rhapsido (remibrutinib) for chronic spontaneous urticaria in adults with inadequate response to H1-antihistamines.
  • Decision makes Rhapsido first oral targeted treatment authorized for CSU in Europe.
  • Novartis said Rhapsido will be taken twice daily with no lab monitoring required.


Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Novartis AG published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202604270115OMX_____CNEWS_EN_GNW1001178018_en) on April 27, 2026, and is solely responsible for the information contained therein.

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