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临床试验/NCT02777567
NCT02777567已完成不适用

Open Label, Multicenter, Real World Treatment Study of Single Agent Tagrisso for Patients With Advanced/Metastatic Epidermal Growth Factor Receptor (EGFR) T790M Mutation-Positive Non-Small Cell Lung Cancer (NSCLC), Who Have Progressed on or After EGFR Tyrosine Kinase Receptor (TKI) Therapy

AstraZeneca1 个研究点 分布在 1 个国家目标入组 315 人开始时间: 2016年9月29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
AstraZeneca
入组人数
315
试验地点
1
主要终点
Proportion (%) of patients with adverse events (AEs), serious adverse events (SAEs) and AEs of special interest (AESI)

研究概览

简要总结

The objectives of this study are to assess the safety and efficacy of single agent Tagrisso (Osimertinib, hereinafter "the study drug") in a real world setting in adult patients with advanced or metastatic, epidermal growth factor receptor (EGFR) T790M mutation-positive Non-Small Cell Lung Cancer (NSCLC), Who Have Progressed on or after EGFR tyrosine kinase receptor (TKI) therapy.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Eligible for, or on active study drug treatment according to the approved label; patients with locally advanced or metastatic, EGFR T790M mutation-positive NSCLC, who have progressed on or after EGFR tyrosine kinase receptor (TKI) therapy
  • Provision of signed and dated written informed consent by the patient or legally acceptable representative

排除标准

  • History of hypersensitivity to excipients of the study drug or to drugs with a similar chemical structure or class to the study drug
  • Pregnancy and/or breast feeding
  • Current participation in any interventional trial

结局指标

主要结局

Proportion (%) of patients with adverse events (AEs), serious adverse events (SAEs) and AEs of special interest (AESI)

时间窗: up to one year

Proportion (%) of patients with adverse events (AEs), serious adverse events (SAEs) and AEs of special interest (AESI)

Severity of (S)AEs

时间窗: up to one year

Severity of (S)AEs

次要结局

  • ORR (Objective response rate), if available(up to one year)
  • PFS (Progression free survival), if available(up to one year)

研究者

发起方
AstraZeneca
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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