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Eurand’s Zentase granted FDA priority review

Eurand has said that the FDA accepted and has granted priority review for Zentase new drug application.

Zentase is a porcine-derived pancreatic enzyme replacement therapy which is being developed to treat pancreatic insufficiency.

Gearoid Faherty, CEO of Eurand, said: “We understand that the typical FDA review period of a drug with priority review status is six months versus a standard 10-month review. In the interim, we remain focused on the build-out of our US specialty sales force in preparation for the potential commercialization of Zentase.”