Chimerix announces FDA acceptance and priority review of new drug application for dordaviprone as treatment for recurrent H3 K27M mutant diffuse glioma

Chimerix

18 February 2025 - PDUFA target action date of 18 August 2025.

Chimerix today announced the US FDA has accepted its new drug application seeking accelerated approval for dordaviprone as a treatment for patients with recurrent H3 K27M-mutant diffuse glioma.

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Michael Wonder

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Michael Wonder

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Medicine , US , Priority review , Dossier