New Dupixent approval in the USA for CSU
The US Food and Drug Administration (FDA) has granted another approval for Dupixent (dupilumab), for the treatment of adults and adolescents aged 12 years and older with chronic spontaneous urticaria (CSU) who remain symptomatic despite histamine-1 (H1) antihistamine treatment.
This is the latest indication for French pharma major Sanofi’s (Euronext: SAN) blockbuster Dupixent, for which global net sales reached around 13.1 billion euros ($14.1 billion) last year, marking a 23% year-over-year increase, with analysts projecting annual revenue to exceed 20 billion euros by 2030, before patent expiration and biosimilar competition kick in.
Market size and competition
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