戴纳基（Dyne Therapeutics）宣布，其针对外显子51型杜氏肌营养不良症（DMD）的在研药物Z-rostudirsen的生物制品许可申请（BLA）已获得美国食品药品监督管理局（FDA）的受理。这一进展标志着该疗法向潜在获批迈出了关键一步。
戴纳基（Dyne Therapeutics）宣布，其针对外显子51型杜氏肌营养不良症（DMD）的在研药物Z-rostudirsen的生物制品许可申请（BLA）已获得美国食品药品监督管理局（FDA）的受理。这一进展标志着该疗法向潜在获批迈出了关键一步。
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