研究项目库 / NCT06465069

LY4052031用于实体瘤的I 期研究

这是一项关于实体瘤的I 期研究,登记的药物或干预包括LY4052031,当前状态为招募中。登记地点显示中国北京、广州、上海有研究中心记录。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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这是一项关于实体瘤的I 期研究,登记的药物或干预包括LY4052031,当前状态为招募中。登记地点显示中国北京、广州、上海有研究中心记录。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

LY4052031 · I 期

登记条件中文摘要

年龄范围:18岁及以上

登记的基本范围为不限性别,年龄18岁及以上;以下仅摘录8项专业入选条件,需结合英文原文并由研究团队确认。

登记记录列出8项主要排除条件,具体医学含义需结合英文原文并由研究团队确认。

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
  • Sun Yat-sen University Cancer Center · 广州
  • Renji Hospital, Shanghai Jiaotong University School of Medicine · 上海

入选条件原文摘录

以下为摘录,请打开原始登记查看完整入排标准。

  • * Have one of the following solid tumor cancers:
  • Cohort A1: urothelial carcinoma, triple negative breast cancer, non-small cell lung cancer, esophageal cancer, pancreatic cancer, ovarian cancer, cervical cancer (squamous cell carcinoma), head and neck squamous cell carcinoma or prostate cancer
  • Cohort A2/B1/B2: urothelial carcinoma
  • Cohort C: triple negative breast cancer, non-small cell lung cancer, ovarian cancer, cervical cancer, HNSCC (head and neck squamous cell carcinoma), esophageal cancer, pancreatic cancer, or prostate cancer
  • * Prior Systemic Therapy Criteria:
  • Cohort A1/C: Individual has received all standard therapies for which the participant was deemed to be an appropriate candidate by the treating investigator; OR there is no standard therapy available for the disease. There is no restriction on number of prior therapies
  • Cohort A2/B1/B2: Individual must have received at least one prior regimen in the advanced or metastatic setting. There is no restriction on number of prior therapies.
  • * Prior enfortumab vedotin specific requirements:

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:NCT06465069;登记信息更新于 2026-10-02;本站同步于 2026-10-08。

查看原始登记记录