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2026 ESMO LBA｜信达生物宣布坦康阿妥塔单抗（CLDN18.2 ADC）国际多中心Ⅲ期胃癌研究达到PFS和OS双主要终点

注册性临床III期G-HOPE-001研究达到双主要终点：在既往接受过治疗的CLDN18.2阳性胃癌患者中，坦康阿妥塔单抗显著且具有临床意义地改善总生存期（OS）和无进展生存期（PFS） 坦康阿妥塔单抗展现出优异的安全性特征，胃肠道不良事件发生率低 坦康阿妥塔单抗是全球首个申报NDA的CLDN18.2 ADC 美国旧金山和中国苏州 2026年10月23日 /美通社/ -- 信达生物制药集团（香港联交所股票代码：01801），一家致力于研发、生产和销售肿瘤、心血管及代谢、自身免疫、眼科等重大疾病领域创新药物的生物制药公司宣布，坦康阿妥塔单抗(IBI343;武田研发代号:TAK-921)治疗 Claudin(CLDN)18.2 阳性、既…

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