金吾财讯 | 和黄医药(00013)宣布，集团自主研发的化合物赛沃替尼（savolitinib）、HMPL-306（ranosidenib）、呋喹替尼（fruquintinib）和索凡替尼（surufatinib）的数项研究的最新及更新后的数据将于2025年5月30日至6月3日在美国芝加哥召开的2025年美国临床肿瘤学会（ASCO）年会上公布。SACHI中国III期研究的结果将以最新突破性口头报告的形式公布，该研究旨在评估赛沃替尼联合奥希替尼（osimertinib）用于一线表皮生长因子受体（“EGFR”）抑制剂治疗后疾病进展的EGFR突变阳性伴MET扩增的局部晚期或转移性非小细胞肺癌患者。SACHI在预设的中期分析中已达到预设的主要终点无进展生存期（“PFS”）。SACHI研究的数据支持了该口服疗法的新药上市申请，该申请已于中国获受理并纳入优先审评。
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