FDA grants priority review to Genentech’s Esbriet (pirfenidone) for unclassifiable interstitial lung disease

Genentech

21 January 2021 - Genentech announced today that the U.S. FDA has accepted the company’s supplemental new drug application  and granted priority review for Esbriet (pirfenidone) for the treatment of unclassifiable interstitial lung disease. 

The FDA is expected to make a decision on approval by May 2021.

Read Genentech press release

Michael Wonder

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Michael Wonder

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Medicine , US , Priority review , Dossier