Avidity Biosciences宣布Del-Zota治疗DMD44获得美国FDA积极的生物制品许可申请预备会议反馈,计划于2026年第一季度提交申请

美股速递
Oct 13

Avidity Biosciences宣布,该公司针对Del-Zota治疗DMD44适应症与美国食品药品监督管理局(FDA)举行的生物制品许可申请预备会议取得积极进展。公司计划于2026年第一季度正式提交相关申请。

这一积极的监管里程碑为Del-Zota在DMD44治疗领域的后续开发奠定了重要基础,标志着该疗法向商业化迈出了关键一步。

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