Sanofi’s bullous pemphigoid treatment given FDA priority review
Sanofi has announced that the US Food and Drug Administration (FDA) has accepted its supplemental biologics licence application (sBLA) for priority review for the treatment of bullous pemphigoid (BP). The sBLA is for Dupixent (dupilumab), which has already received regulatory approvals in more than 60 countries for certain patients with atopic dermatitis, asthma, chronic rhinosinusitis with nasal polyps, eosinophilic oesophagitis, prurigo nodularis, chronic spontaneous urtica