复星医药：控股子公司FKC289注射液获临床试验批准

每日经济新闻04-14

每经AI快讯，4月14日，复星医药(600196.SH)公告称，公司控股子公司复星凯瑞收到国家药监局关于同意FKC289注射液开展I/II期临床试验的批准。该药品为靶向BCMA和CD19的基因修饰CAR-T细胞产品，拟用于复发/难治原发性轻链淀粉样变及复发/难治膜性肾病的治疗。（文章来源：每日经济新闻）

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