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).
The US Food and Drug Administration (FDA) has agreed to review Emergent BioSolutions’ Biologics License Application (BLA) for AV7909 (Anthrax Vaccine Adsorbed, Adjuvanted).