万达生物制药宣布美国FDA为Hetlioz®时差障碍适应症召开里程碑式听证会，系40余年来首次新药审批听证_老虎社区_美港股上老虎

万达生物制药宣布美国FDA为Hetlioz®时差障碍适应症召开里程碑式听证会，系40余年来首次新药审批听证

美股速递03-03

万达生物制药宣布，美国食品药品监督管理局已为其药物Hetlioz®用于治疗时差障碍的申请召开了一次具有里程碑意义的听证会。此次听证会是FDA超过40年来首次针对新药审批举行的听证会，标志着监管程序的一个重要突破。

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