Finding studies
Finding studies
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Lead
Jonsson Comprehensive Cancer Center
OBJECTIVES: * Determine the clinical effect of monoclonal antibody ABX-EGF, determined by the PSA response, in patients with hormone-resistant prostate cancer with rising PSA values without metastasis. * Determine the pharmacokinetics and safety profile (including immunogenicity) of this drug in these patients. * Determine the overall survival of patients treated with this drug. * Determine the time to disease progression and time to PSA progression in patients treated with this drug. OUTLINE: This is a multicenter study. Patients receive monoclonal antibody ABX-EGF IV over 1 hour once weekly. Treatment continues every 8 weeks for up to 6 courses in the absence of disease progression or unacceptable toxicity. Patients are followed every 3 months for 2 years. PROJECTED ACCRUAL: Approximately 30-50 patients will be accrued for this study.
Age
18–120
Sex
MALE
Healthy volunteers
Not accepted
