Theriva™ Biologics 宣布，已成功与美国食品药品监督管理局（FDA）就其在研药物Vcn-01用于治疗转移性胰腺导管腺癌的三期临床试验设计，完成了二期结束会议，并获得了积极的反馈。
此次会议的积极结果为推进Vcn-01的关键性三期临床试验奠定了坚实基础，标志着该疗法在针对这一难治性癌症的研发进程中迈出了重要一步。
Theriva™ Biologics 宣布，已成功与美国食品药品监督管理局（FDA）就其在研药物Vcn-01用于治疗转移性胰腺导管腺癌的三期临床试验设计，完成了二期结束会议，并获得了积极的反馈。
此次会议的积极结果为推进Vcn-01的关键性三期临床试验奠定了坚实基础，标志着该疗法在针对这一难治性癌症的研发进程中迈出了重要一步。
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