步长制药最新公告：控股子公司药品临床试验申请获受理

证券之星08-19

步长制药(603858.SH)公告称，公司控股子公司四川泸州步长生物制药有限公司的“BC008-1A注射液”新增适应症临床试验申请获国家药监局受理。该药品为重组抗PD-1/TIGIT人源化双特异性抗体注射液，拟新增适应症为联合贝伐珠单抗用于成人复发CNSWHO4级脑胶质瘤治疗。截至2026年7月31日，该项目研发投入约1.15亿元。目前国内外尚无同靶点双功能特异性抗体药物获批上市。

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。

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