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公司控股子公司上海複宏漢霖生物技術股份有限公司及其控股子公司（以下合稱“複宏漢霖”）於近日收到國家藥品監督管理局關於同意其自主研發的HLX53（即抗TIGIT的Fc融合蛋白）聯合漢斯狀？（即斯魯利單抗注射液）和漢貝泰？（即貝伐珠單抗注射液）一線治療局部晚期或轉移性肝細胞癌（HCC）開展臨床試驗的批準。4月1 |
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