Head and Neck Cancer Clinical Trial
Official title:
A Phase III Study Evaluating the Standard Radiation Therapy and Chemotherapy Regimen, With or Without Nimotuzumab, in Unresectable, Locally Advanced Epidermoid Carcinoma of the Head and Neck
Primary: to compare the overall survival defined as the time elapsed between the
randomization date and death due to any cause, in both treatment groups.
Secondary: to compare the progression-free survival, incidence of locoregional failure, site
of the first recurrence/progression, objective response rate assessment, quality of life
assessment and incidence of adverse events.
This is a phase III, superiority, national, open-label, randomized, and two-arm study.
Patients' enrollment will be performed only after approval by competent regulatory
authorities and it will last up to 12 months.
All patients taking part in the study must sign an informed consent. The patients will have
stage III or IV, unresectable head and neck SCC, performance status 0 or 1.
Randomization and treatment assignment will be performed by a company specifically
contracted for such purpose and will be per research site and disease stage, 1:1
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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