复星医药(600196.SH)控股子公司HLX37注射液获临床试验批准

智通财经12-01

智通财经APP讯，复星医药(600196.SH)发布公告，近日，公司控股子公司上海复宏汉霖生物技术股份有限公司及其控股子公司(合称“复宏汉霖”)收到国家药品监督管理局关于同意HLX37注射液(即重组人源化抗PD-L1与抗VEGF双特异性抗体注射液;简称“HLX37”)用于治疗晚期/转移性实体瘤患者开展临床试验的批准。复宏汉霖拟于条件具备后于中国境内开展HLX37的Ⅰ期临床试验。

HLX37是集团自主研发的重组人源化抗PD-L1与抗VEGF双特异性抗体，拟用于治疗晚期/转移性实体瘤。截至目前的临床前研究表明，HLX37能够抑制肿瘤生长，且具有良好的安全性。

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