Sanofi and Regeneron Pharmaceuticals Inc. are successfully executing on their pipeline-in-a-molecule strategy for Dupixent (dupilumab), announcing the US Food and Drug Administration’s approval of a third indication for the IL-4/IL-13 blocker on 26 June. The new indication is for chronic rhinosinusitis patients with nasal polyposis (CRSwNP) whose disease is not controlled, adding to Dupixent's existing approvals in atopic dermatitis and moderate to severe asthma.
The two partners have expressed big ambitions for Dupixent as a treatment for a range of conditions characterized by type...








