Finding studies
Finding studies
Take this into the appointment.
Saves the questions and what to expect into your notes, next to the visit they belong to.
Lead
University of Chicago
With
OBJECTIVES: * Compare the time to progression in patients with hormone refractory prostate cancer treated with dexamethasone with or without SU5416. * Determine the differences in PSA kinetics and PSA hazard score between these two regimens in this patient population. * Determine the objective response rate and time to development of new lesions in these patients treated with SU5416. * Determine the toxicity of SU5416 in these patients. OUTLINE: This is a randomized study. Patients are randomized to one of two treatment arms. * Arm I: Patients receive oral dexamethasone once a day 6 days a week. Treatment continues until disease progression, at which time patients cross over to arm II. * Arm II: Patients receive oral dexamethasone as in arm I followed by SU5416 IV over 60 minutes twice weekly for 4 weeks. A smaller dose of dexamethasone is administered the day after SU5416. Treatment continues for a minimum of 2 courses in the absence of unacceptable toxicity or disease progression. PROJECTED ACCRUAL: A total of 60 patients (30 per arm) will be accrued for this study within 16 months.
Age
18–any
Sex
MALE
Healthy volunteers
Not accepted
