研究项目库 / NCT06901531

zolbetuximab用于Locally Advanced Unresectable Gastroesophageal Junction (GEJ) Adenocarcinoma or Cancer的III 期研究

这是一项关于Locally Advanced Unresectable Gastroesophageal Junction (GEJ) Adenocarcinoma or Cancer的III 期研究,登记的药物或干预包括zolbetuximab;Pembrolizumab;Capecitabine;Oxaliplatin;Folinic acid (leucovorin or local equivalent);5-fluorouracil (5-FU);Placebo,当前状态为招募中。登记地点显示中国合肥、福州、广州、哈尔滨等城市有研究中心记录。是否仍有名额以及是否值得进一步询问,需要向研究中心确认。

一分钟看懂

这是一项关于Locally Advanced Unresectable Gastroesophageal Junction (GEJ) Adenocarcinoma or Cancer的III 期研究,登记的药物或干预包括zolbetuximab;Pembrolizumab;Capecitabine;Oxaliplatin;Folinic acid (leucovorin or local equivalent);5-fluorouracil (5-FU);Placebo,当前状态为招募中。登记地点显示中国合肥、福州、广州、哈尔滨等城市有研究中心记录。是否仍有名额以及是否值得进一步询问,需要向研究中心确认。

药物或干预

zolbetuximab;Pembrolizumab;Capecitabine;Oxaliplatin;Folinic acid (leucovorin or local equivalent);5-fluorouracil (5-FU);Placebo · III 期

中国哪些地方有记录

以下地点来自登记信息,不代表此刻仍有名额;请向研究中心确认最新情况。

  • Anhui Provincial Cancer Hospital · 合肥
  • Fujian Provincial Hospital - Department of Medical Oncology · 福州
  • Sun Yat-sen University - Cancer Center · 广州
  • Harbin Medical University Cancer Hospital - Oncology · 哈尔滨
  • Henan Cancer Hospital - Oncology · 郑州
  • Hubei Cancer Hospital - Oncology · 武汉
  • Qinghai University Affiliated Hospital · 西宁
  • Renji Hospital Shanghai Jiaotong Univ School of Medicine · 上海
  • Ruijin Hospital of Shanghai Jiaotong University School of Medicine · 上海
  • Sichuan Cancer Hospital · 成都
  • Tianjin Medical University General Hospital · 天津
  • The First Affiliated Hospital of Zhejiang University · 杭州
  • Affiliated Hospital of Hebei University · 保定
  • Peking Union Medical College Hospital - Dongdan Campus · 北京

公开的入选条件

  • * Participant has histologically confirmed gastric or Gastroesophageal Junction (GEJ) adenocarcinoma.
  • * Participant has radiographically confirmed, locally advanced, unresectable or metastatic disease within 28 days prior to randomization.
  • * Participant has radiologically evaluable disease (measurable and/or nonmeasurable) according to Response Evaluation Criteria in Solid Tumors (RECIST) V1.1, ≤ 28 days prior to randomization. For participants with only 1 evaluable lesion and prior radiotherapy
  • * Participant has Eastern Cooperative Oncology Group Performance Status (ECOG) performance status 0 to 1.
  • * Participant has predicted life expectancy ≥ 12 weeks.
  • * Participant must be a candidate to receive mFOLFOX6 or CAPOX and pembrolizumab.
  • * Female participant is not pregnant and at least 1 of the following conditions apply:
  • Not a woman of child bearing potential (WOCBP)

联系前需要确认

请继续确认中心是否启动、疾病分型、既往治疗、检查费用和知情同意安排。

查看登记信息

登记号:NCT06901531;登记信息更新于 2026-09-15。

查看原始登记记录