Revance submits biologics license application to the FDA for DAXI to treat glabellar (frown) lines

Revance Therapeutics

25 November 2019 - Revance Therapeutics today announced the Company has submitted a biologics license application to the U.S. FDA for daxibotulinumtoxinA for Injection (DAXI) in the treatment of moderate to severe glabellar (frown) lines. 

The submission includes results from the SAKURA Phase 3 trials, which is the largest aesthetic neuromodulator clinical program ever conducted for the treatment of glabellar frown lines.

Read Revance press release

Michael Wonder

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Michael Wonder

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Medicine , US , Dossier