[Translation] An open-label, multicenter, Phase I clinical study of ATG-022 in patients with advanced/metastatic solid tumors
这是一项 ATG-022 在晚期实体瘤患者中的 I 期、多中心、开放性、剂量探索研究。研究设计包括剂量递增阶段(该阶段将入组晚期/转移性实体瘤受试者)和剂量扩展阶段(该阶段将入组具有 Claudin 18.2 阳性表达的选定晚期/转移性实体瘤受试者,以定义的最大耐受剂量[MTD]和/或 II 期推荐剂量[RP2D]给药)以进一步评价 ATG-022 的安全性、耐受性和疗效。
[Translation] This is a Phase I, multicenter, open-label, dose-finding study of ATG-022 in patients with advanced solid tumors. The study design includes a dose escalation phase (which will enroll subjects with advanced/metastatic solid tumors) and a dose expansion phase (which will enroll selected subjects with advanced/metastatic solid tumors with positive Claudin 18.2 expression, dosed at a defined maximum tolerated dose [MTD] and/or recommended Phase II dose [RP2D]) to further evaluate the safety, tolerability and efficacy of ATG-022.