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复星医药(600196.SH)：控股子公司获药品临床试验批准

Fosun Pharmaceuticals (600196.SH): Holding subsidiary approved for drug clinical trials

Gelonghui Finance · Apr 17 04:37

FOSUN PHARMA +1.27% Shanghai Fosun Pharmaceutical +1.90%

格隆汇4月17日丨复星医药(600196.SH)公布，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于近日收到国家药品监督管理局关于同意其自主研发的HLX53（即抗TIGIT的Fc融合蛋白）联合汉斯状（即斯鲁利单抗注射液）和汉贝泰（即贝伐珠单抗注射液）一线治疗局部晚期或转移性肝细胞癌（HCC）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（不包括港澳台地区）开展该治疗方案的II期临床试验。

Gelonghui, April 17 | Fosun Pharmaceutical (600196.SH) announced that its holding subsidiary Shanghai Fuhong Hanlin Biotechnology Co., Ltd. and its holding subsidiary recently received approval from the National Drug Administration to conduct clinical trials with HLX53 (i.e. anti-Tigit FC fusion protein) combined with Hans form (i.e. slulizumab injection) and Hanbetai (i.e. bevacizumab injection) for first-line treatment of locally advanced or metastatic hepatocellular carcinoma (HCC). Fu Hong Hanlin plans to conduct phase II clinical trials of this treatment plan in China (excluding Hong Kong, Macao and Taiwan regions) when conditions are met.

Disclaimer: This content is for informational and educational purposes only and does not constitute a recommendation or endorsement of any specific investment or investment strategy. Read more

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