研究项目库 / NCT07811193

VVD-133214用于结直肠癌的II 期研究

这是一项关于结直肠癌的II 期研究,登记的药物或干预包括VVD-133214;Pembrolizumab,当前状态为招募中。登记地点显示中国蚌埠、北京、福州、广州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。

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这是一项关于结直肠癌的II 期研究,登记的药物或干预包括VVD-133214;Pembrolizumab,当前状态为招募中。登记地点显示中国蚌埠、北京、福州、广州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

VVD-133214;Pembrolizumab · II 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。

  • The First Affiliated Hospital of Bengbu Medical College · 蚌埠
  • Beijing Cancer Hospital - Oncology Department · 北京
  • Fujian Cancer Hospital · 福州
  • The Sixth Affiliated Hospital, Sun Yat-sen University · 广州
  • Harbin Medical University Cancer Hospital · 哈尔滨
  • Tongji Hospital affiliated to Tongji Medical College of Huazhong University of Science & Technology · 武汉
  • Shandong University - Shandong Cancer Hospital · 济南
  • Zhongshan Hospital, Fudan University · 上海
  • West China Hospital Sichuan University · 成都
  • Yunnan Cancer Hospital · 昆明
  • Sir Run Run Shaw Hospital, Zhejiang Univ. School of Medicine - Oncology Department · 杭州
  • Zhejiang Cancer Hospital · 杭州

公开的入选条件

  • * Eastern Cooperative Oncology Group (ECOG) performance-status score of 0 or 1
  • * Have a known microsatellite instability (MSI) and/or deficient mismatch repair (dMMR) tumor status confirmed per local standard of care (SoC), and have histologically or cytologically documented advanced (unresectable and/or metastatic) colorectal adenocarci
  • * No prior systemic treatment for metastatic disease and not amenable to curative resection
  • * Participants must have documented MSI and/or dMMR tumor status determined as part of the routine diagnostic workup in a certified laboratory
  • * Availability of formaldehyde-fixed paraffin-embedded (FFPE) archival tumor tissue for submission to Sponsor/central laboratory for retrospective central testing including a copy of a redacted pathology report if available
  • * Presence of measurable disease according to RECIST v1.1
  • * Adequate hematologic and end-organ function, defined using laboratory results obtained within 14 days prior to first dose of study treatment
  • * Females of childbearing potential must have negative serum pregnancy test before starting study treatment

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:NCT07811193;登记信息更新于 2026-09-16。

查看原始登记记录