Finding studies
Finding studies
Take this into the appointment.
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Lead
European Organisation for Research and Treatment of Cancer - EORTC
OBJECTIVES: * Assess the activity of MEN-10755 in patients with progressive hormone-refractory adenocarcinoma of the prostate. * Determine the rate and duration of objective PSA response in patients treated with this drug. * Determine the clinical response rate in patients with measurable disease treated with this drug. * Determine the acute side effects of this drug in these patients. OUTLINE: This is a multicenter study. Beginning within 2 weeks after the last PSA measurement, patients receive MEN-10755 IV over 30 minutes on day 1. Treatment repeats every 3 weeks for at least 4 courses in the absence of disease progression or unacceptable toxicity. Patients who achieve a complete or partial response continue to receive additional courses. Patients who achieve stable disease may receive more than 4 courses at the discretion of the investigator. Patients are followed every 6 weeks until disease progression or initiation of a new therapy. PROJECTED ACCRUAL: A total of 18-32 patients will be accrued for this study.
Age
18–any
Sex
MALE
Healthy volunteers
Not accepted
