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临床试验/NCT04616040
NCT04616040尚未招募不适用

A Non-interventional Registration Study Evaluating the Usage of Camrelizumab in the Treatment of Unresectable Locally Advanced/Recurrent or Metastatic Chinese Patients With Esophageal Cancer

Peking University1 个研究点 分布在 1 个国家目标入组 1,030 人开始时间: 2020年12月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
1,030
试验地点
1
主要终点
Adverse events of Camrelizumab

研究概览

简要总结

The trial is a multi-center, open, observational registration study, which aims to evaluate the safety and efficacy of Camrelizumab (anti-PD-1 antibody) in the treatment of Chinese patients with advanced esophageal cancer in the real world.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Sign informed consent and voluntarily participate in this study.
  • Unresectable locally advanced/recurring or distant metastatic esophageal cancer patients confirmed by histology or cytology (AJCC 8th edition);
  • Unresectable locally advanced patients who are unable or unable to receive radical treatment (including radical radio chemotherapy or radical radiotherapy, etc.) may be considered for inclusion;
  • Patients who progress or relapse after neoadjuvant or adjuvant therapy may also be considered for inclusion;
  • Age ≥ 18 years old;
  • The investigator determines that the patient can receive Camrelizumab as a single agent or combination therapy.

排除标准

  • Evidence suggests that the patient is pregnant or breastfeeding;
  • Other drug blinded clinical trials are currently underway;
  • Other situations that are not suitable for inclusion in this study.

研究组 & 干预措施

unresectable locally advanced/recurrent or metastatic esophageal cancer

干预措施: Camrelizumab (Drug)

结局指标

主要结局

Adverse events of Camrelizumab

时间窗: an expected average of 24 months

especially Occurrence of ≥Grade 3 immune-related AEs

次要结局

  • Progression-free Survival (PFS)(an expected average of 24 months)
  • Objective Response Rate (ORR)(an expected average of 24 months)
  • Adverse events of Camrelizumab(an expected average of 24 months)
  • Overall Survival(an expected average of 24 months)

研究者

发起方
Peking University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Shen Lin

Professor

Peking University

研究点 (1)

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