Pharvaris N.V. 宣布，美国食品药品监督管理局（FDA）已正式受理其新药Deucrictibant Ir用于遗传性血管水肿急性发作按需治疗的新药申请。这一进展标志着该药物在监管审批流程中迈出了关键一步。
Pharvaris N.V. 宣布，美国食品药品监督管理局（FDA）已正式受理其新药Deucrictibant Ir用于遗传性血管水肿急性发作按需治疗的新药申请。这一进展标志着该药物在监管审批流程中迈出了关键一步。
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