中源协和：VUM02/03共11个适应症已获临床试验批准

证券之星08-05

证券之星消息，中源协和(600645)08月05日在投资者关系平台上答复投资者关心的问题。

投资者提问：公司VUM02干细胞注射液已获批新冠治疗Ⅱ/lll期临床试验与重症/危重症肺炎Ⅱ/lll期临床试验，请问目前有没有患者入组？

中源协和回复：尊敬的投资者，您好。公司全资子公司武汉光谷药业自主研发的人脐带间充质干/ 基质细胞产品VUM02/03共11个适应症已获临床试验批准。其中重型/危重型新型冠状病毒感染、重型/危重型肺炎获批Ⅱ/Ⅲ期临床试验；肺炎后进展性肺纤维化获批Ⅱa期临床试验；特发性肺纤维化完成Ⅰ期所有受试者给药，正在数据整理和随访中；失代偿期肝硬化已启动Ⅰb/Ⅱ期临床试验；激素治疗失败的 II 度至 IV 度急性移植物抗宿主病I期多次给药首例受试者已完成入组给药。

本文数据来源于上海证券交易所e互动，仅供参考不构成投资建议。

责任编辑：刘浩然

免责声明：本文观点仅代表作者个人观点，不构成本平台的投资建议，本平台不对文章信息准确性、完整性和及时性做出任何保证，亦不对因使用或信赖文章信息引发的任何损失承担责任。

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