Skip to main content
Clinical Trials/NCT02131155
NCT02131155
Terminated
Phase 3

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 sites in 3 countries36 target enrollmentJuly 17, 2014

Overview

Phase
Phase 3
Intervention
Afatinib
Conditions
Head and Neck Neoplasms
Sponsor
Boehringer Ingelheim
Enrollment
36
Locations
16
Primary Endpoint
Disease Free Survival (DFS)
Status
Terminated
Last Updated
7 years ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
July 17, 2014
End Date
August 22, 2016
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Arms & Interventions

Afatinib (BIBW2992)

Once daily

Intervention: Afatinib

Placebo

Once daily

Intervention: Placebo

Outcomes

Primary Outcomes

Disease Free Survival (DFS)

Time Frame: 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.

Secondary Outcomes

  • 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)

Study Sites (16)

Loading locations...

Similar Trials