Praxis Precision Medicines公司披露，美国食品药品监督管理局（FDA）已为其在研药物Relutrigine设定了处方药使用者费法案（PDUFA）的目标行动日期，定于2026年9月27日。
Praxis Precision Medicines公司披露，美国食品药品监督管理局（FDA）已为其在研药物Relutrigine设定了处方药使用者费法案（PDUFA）的目标行动日期，定于2026年9月27日。
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