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康方生物(09926.HK)治疗晚期宫颈癌新药获美国授快速审批通道资格
阿思达克 08-13 08:12
康方生物(09926.HK)公布,其核心自主研发的、全球首创的新型肿瘤免疫治疗双特异性抗体新药PD-1/CTLA-4(AK104)治疗晚期宫颈癌已经获得美国食品药品监督管理局(FDA)授予快速审批通道资格(FTD)。

这是继2020年4月AK104单药针对二线治疗复发或转移性宫颈癌的临床研究获得FDA的批准开展注册性临床研究後的又一重大进展。

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