Sanofi and Regeneron announce marketing authorisation application for Dupixent (dupilumab) accepted for review by the EMA

Sanofi

8 December 2016 - Sanofi and Regeneron Pharmaceuticals today announced that the EMA has accepted for review the marketing authorisation application for Dupixent (dupilumab) for the treatment of adults with moderate-to-severe atopic dermatitis who are candidates for systemic therapy. 

The investigational biologic therapy Dupixent inhibits signalling of IL-4 and IL-13, two key cytokines required for the type 2 (including Th2) immune response, which is believed to be a major driver in the pathogenesis of the disease.

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Michael Wonder

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Michael Wonder

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Medicine , Europe , Submission