天士力最新公告：子公司注射用重组人尿激酶原获临床试验通知书扩展急性缺血性卒中适应症时间窗

证券之星07-17

天士力(600535.SH)公告称，公司全资子公司天士力生物收到国家药监局核准签发的《药品临床试验通知书》，获批开展注射用重组人尿激酶原(普佑克)用于发病4.5至24小时急性缺血性卒中患者的临床试验。该药品为1类生物创新药，此前已获批用于发病4.5小时内患者的静脉溶栓治疗。截至目前，相关研发投入为54.85万元。

以上内容为证券之星据公开信息整理，仅供参考不构成投资建议。

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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