Head and Neck Cancer Clinical Trial
Official title:
An Open-Labeled Randomized Parallel Group Trial of Zalutumumab, a Human Monoclonal Anti-EGFr Antibody, in Combination With Best Supportive Care (BSC) vs BSC, in Pts With Non-Curable SCCHN Who Have Failed Standard Platinum-Based Chemotherapy
The purpose of this study is to investigate if zalutumumab in combination with Best Supportive Care (BSC) is superior to BSC in non-curable patients with head and neck cancer
This is an open parallel group trial. Patients will be randomized in a 2:1 manner to receive
either treatment with zalutumumab in combination with Best Supportive Care (BSC) or BSC.
Patients randomized to treatment with zalutumumab in combination with BSC will receive
weekly infusions with zalutumumab starting with a loading dose (8mg/kg) followed by weekly
maintenance doses until disease progression, intercurrent illness preventing further
administration, unacceptable toxicity or patient decision. After Visit 2 the patient should
be evaluated for presence of skin rash prior to each infusion to allow dose titration.
Individual dose titration until the patient develops grade 2 skin rash will be applied. The
maximum dose used in study will be 16 mg/kg.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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