FDA approves Novartis’ Rhapsido for CSU treatment
Novartis has obtained approval from the US Food and Drug Administration (FDA) for Rhapsido (remibrutinib) to treat adult patients suffering from chronic spontaneous urticaria (CSU).
Novartis has obtained approval from the US Food and Drug Administration (FDA) for Rhapsido (remibrutinib) to treat adult patients suffering from chronic spontaneous urticaria (CSU).
Timber Pharmaceuticals has received orphan drug designation from the European Commission (EC) for TMB-001 to treat X-linked recessive ichthyosis (XLRI).