跳至主要内容
临床试验/NCT02131155
NCT02131155终止3 期

A Randomised, Double-blind, Placebo-controlled, Phase III Study to Evaluate the Efficacy and Safety of Afatinib (BIBW 2992) as Adjuvant Therapy After Chemo-radiotherapy in Primary Unresected Patients With Stage III, IVa, or IVb Loco-regionally Advanced Head and Neck Squamous Cell Carcinoma

Boehringer Ingelheim16 个研究点 分布在 3 个国家目标入组 36 人开始时间: 2014年7月17日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
终止
入组人数
36
试验地点
16
主要终点
Disease Free Survival (DFS)

研究概览

简要总结

This randomised, double-blind phase III trial will be performed in patients with head and neck squamous cell carcinoma (HNSCC). The objectives of the trial are to compare the efficacy and safety of afatinib (BIBW 2992) with placebo as adjuvant therapy to patients who have received definitive chemo-radiotherapy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

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

  • 未提供

研究组 & 干预措施

Afatinib (BIBW2992)

Experimental

Once daily

干预措施: Afatinib (Drug)

Placebo

Placebo Comparator

Once daily

干预措施: Placebo (Drug)

结局指标

主要结局

Disease Free Survival (DFS)

时间窗: up to 4 years

DFS, defined as the number of days from the date of randomisation to the date of tumour recurrence/ Second Primary Tumours (SPT) or death from any cause, whichever occurred first. For patients with known date of tumour recurrence/SPT (or death), the event date was the date of tumour recurrence/SPT or the date of death, whichever came first, i.e. DFS \[day\] = minimum (date of tumour recurrence/SPT, date of death) - date of randomisation +1. For patients known to be alive and without tumour recurrence/SPT by the end of trial or follow-up visit, they were censored at the date of last imaging when the patient was known to be disease-free and alive: DFS (censored) \[days\] = date of last imaging when the patient was known to be diseasefree and alive - date of randomisation + 1. The Kaplan-Meier (KM) method was to be used to estimate the median DFS for each treatment group. 95% confidence interval (CI) was to be constructed using the Greenwood variance estimate.

次要结局

  • Health Related Quality of Life (HRQOL)(up to 4 years)
  • Disease Free Survival (DFS) Rate at 2 Years(up to 2 years)
  • Overall Survival (OS)(up to 4 years)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (16)

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