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FDA and EMA Accept Regulatory Submissions for Vorasidenib for IDH-Mutant Diffuse Glioma
Vorasidenib has been granted regulatory submission acceptance by the FDA and EMA for IDH-mutant diffuse glioma.
Claude bertrand
Susan pandya
European commission
Cancer metabolism global development oncology immuno
Meeting of the society for neuro
European medicines agency
Research development
Marketing authorization application
New england journal
Cancer metabolism global development oncology
Prescription drug user fee act
Idh mutant diffuse glioma
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