EC nod for three additional Nucala indications

17 November 2021

The European Commission has approved Nucala (mepolizumab), a monoclonal antibody that targets interleukin-5 (IL-5), for use in three additional eosinophil-driven diseases, UK pharma major GlaxoSmithKline (LSE: GSK) announced today.

This authorization follows positive opinions recommended by the Committee for Medicinal Products for Human Use and authorizes mepolizumab for use as an add on treatment in hypereosinophilic syndrome (HES), eosinophilic granulomatosis with polyangiitis (EGPA) and chronic rhinosinusitis with nasal polyps (CRSwNP). In its previously approved indications, sales of Nucala were £831 million ($1.12 billion) in the first nine months of this year, and grew 26% at constant exchange rates.

Clinical backing

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