Medicus Pharma Ltd.（MDCX）近日迎来重大里程碑——美国食品药品监督管理局（FDA）已正式发出“研究可推进”函件，为其针对戈林综合征患者的NDA注册性Skinject®研究亮起绿灯。这一关键进展，标志着该药物的临床开发迈入新阶段。
Medicus Pharma Ltd.（MDCX）近日迎来重大里程碑——美国食品药品监督管理局（FDA）已正式发出“研究可推进”函件，为其针对戈林综合征患者的NDA注册性Skinject®研究亮起绿灯。这一关键进展，标志着该药物的临床开发迈入新阶段。
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