复星医药子公司FXB0871获批临床试验用于局部晚期或转移性实体瘤

财中社03-31

3月31日，复星医药（600196/02196）发布公告，控股子公司药品获得临床试验批准。公司控股子公司复星医药产业近日收到国家药品监督管理局的批准，允许其开展FXB0871用于局部晚期或转移性实体瘤的I期临床研究。　　该药物是公司与Teva合作开发的PD-1靶向型IL-2融合蛋白，具有增强T细胞活性及降低全身毒性的特点。截至2026年2月，公司针对FXB0871的累计研发投入约为628万元（未经...

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复星医药子公司FXB0871获批临床试验 用于局部晚期或转移性实体瘤

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复星医药子公司FXB0871获批临床试验用于局部晚期或转移性实体瘤