信達生物(01801.HK)對晚期惡性腫瘤臨床研究在中國完成首例患者給藥
信達生物(01801.HK)公布,公司自主開發的重組全人源抗淋巴細胞活化基因3(LAG-3)單克隆抗體(IBI-110)的I期臨床研究完成中國首例患者給藥。
該臨床研究是一項在中國開展的評估IBI-110單藥或聯合達伯舒,重組全人源抗PD-1單克隆抗體,治療晚期惡性腫瘤受試者中的安全性、耐受性和初步抗腫瘤有效性的臨床研究。
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