Galderma provides progress update regarding relabotulinumtoxinA regulatory submission in the US

Galderma

1 July 2026 - Galderma today provided progress updates regarding the regulatory review of its pending biologics license application for relabotulinumtoxinA with the US FDA. 

The Company has received a complete response letter from the FDA with comments related to observations during manufacturing site inspection and analytical method optimization.

Read Galderma press release

Michael Wonder

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Michael Wonder

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Outcome , Medicine , US , Registration