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复星医药(02196.HK)实体瘤治疗药获FDA批准临床试验
阿思达克 06-01 04:33
复星医药(02196.HK)公布,控股子公司Hengenix收到FDA(美国食品药品监督管理局)开於同意重组抗CD73全人源单克隆抗体注射液(即 HLX23)用於晚期实体瘤治疗进行临床试验的函。Hengenix拟於条件具备後於美国进行该新药的临床试验。

至今年4月,集团针对该新药累计研发投入约6,293万人民币。

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