复星医药:控股子公司药品获临床试验批准

同花顺财经
Sep 08, 2025
复星医药公告,控股子公司复星万邦(江苏)医药集团有限公司于近期收到国家药品监督管理局关于同意丁二酸复瑞替尼胶囊用于间变性淋巴瘤激酶(ALK)阳性或者c-ros肉瘤致癌因子-受体酪氨酸激酶(ROS1)阳性的IB期至ⅢA期非小细胞肺癌患者肿瘤根治性切除术后辅助治疗开展临床试验的批准。复星万邦拟于条件具备后于中国境内开展该新药的Ⅲ期临床试验。截至2025年7月,本集团针对该新药的累计研发投入约为4.53亿元。

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