Keeping Track: After COVID Delays, US FDA Approvals At Last For Daxxify, Rolvedon (But A CRL For Alvotech)

The latest drug development news and highlights from the Pink Sheet’s US FDA Performance Tracker.

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The waning of the COVID-19 pandemic was reflected in three FDA decisions issued last week for applications that had been under review long past their user fee goal dates because manufacturing inspections could not be conducted.

Revance Therapeutics, Inc.’s long-acting botulinum toxin Daxxify was approved to improve the appearance of frown lines on 8 September...

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