Hugel resubmits BLA for its botulinum toxin, Letybo to the US FDA

Hugel

1 September 2023 - Expected to obtain the US FDA's approval in the first quarter of 2024.

Hugel announced that the company resubmitted the biologics license application for its botulinum toxin, Letybo (letibotulinumtoxinA) on 31 August (local time), for the indication of glabellar (frown) lines to the US FDA.

Read Hugel press release

Michael Wonder

Posted by:

Michael Wonder

Posted in:

Medicine , US , Dossier