研究项目库 / NCT07676162

SHR-A1811, Oxaliplatin, Levo-leucovorin, Fluorouracil and Bevacizumab用于结直肠癌的III 期研究

这是一项关于结直肠癌的III 期研究,登记的药物或干预包括SHR-A1811, Oxaliplatin, Levo-leucovorin, Fluorouracil and Bevacizumab;Oxaliplatin, Levo-leucovorin, Fluorouracil and Bevacizumab,当前状态为招募中。登记地点显示中国北京有研究中心记录。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III 期研究,登记的药物或干预包括SHR-A1811, Oxaliplatin, Levo-leucovorin, Fluorouracil and Bevacizumab;Oxaliplatin, Levo-leucovorin, Fluorouracil and Bevacizumab,当前状态为招募中。登记地点显示中国北京有研究中心记录。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

SHR-A1811, Oxaliplatin, Levo-leucovorin, Fluorouracil and Bevacizumab;Oxaliplatin, Levo-leucovorin, Fluorouracil and Bevacizumab · 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。

  • Beijing cancer Hospital · 北京

公开的入选条件

  • 1. Subjects voluntarily enroll in the study, sign informed consent, demonstrate good compliance and cooperate with follow-up visits.
  • 2. Aged between 18 and 75 years inclusive, male or female.
  • 3. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
  • 4. Estimated survival expectancy ≥ 12 weeks.
  • 5. Histologically or cytologically confirmed colorectal adenocarcinoma.
  • 6. No prior systemic anti-tumor therapy.
  • 7. Tumor tissue specimen must be provided, either archived within 1 year prior to first study treatment or newly collected fresh specimen.
  • 8. At least one measurable lesion per Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1; the measurable lesion shall not have received prior local therapy such as radiotherapy.

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:NCT07676162;登记信息更新于 2026-09-10。

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