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FDA accepts Ipsen’s biologics license application for Reloxin

Ipsen and Medicis have announced that the FDA has accepted the filing of Ipsen's biologics license application for Reloxin, its botulinum toxin type A, in aesthetic use in the US. This acceptance signifies the start of the review process of the dossier.

In accordance with the agreement between the two parties, Medicis will pay Ipsen approximately $25 million and subject to approval of the biologics license application by the FDA, Medicis will pay to Ipsen a further $75 million and will commercialize Reloxin in the US.