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临床试验/NCT03804554
NCT03804554已完成不适用

Nivolumab in the Treatment of Patients With Non-small Cell Lung Cancer: The Australian Experience

Bristol-Myers Squibb1 个研究点 分布在 1 个国家目标入组 503 人开始时间: 2018年10月3日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
503
试验地点
1
主要终点
Time to treatment failure (TTF)

研究概览

简要总结

This study is to capture and describe the patient and disease characteristics and the outcomes of adult patients with previously-treated advanced NSCLC who have been treated with Nivolumab

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

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

  • 未提供

排除标准

  • Insufficient data available
  • Other protocol defined inclusion/exclusion criteria could apply

结局指标

主要结局

Time to treatment failure (TTF)

时间窗: Approximately 27 months

次要结局

  • Incidence of SAE's(Approximately 27 months)
  • Incidence of re-treatment(Approximately 27 months)
  • Progression free survival rate (PFSR)(Approximately 27 months)
  • Incidence of AE's(Approximately 27 months)
  • Best overall response (BOR)(Approximately 27 months)
  • Overall survival rate (OSR)(Approximately 27 months)
  • Reasons for ceasing treatment(Approximately 27 months)
  • Incidence of patients with brain metastases(Approximately 27 months)

研究者

发起方
Bristol-Myers Squibb
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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