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Treatment Protocol to Monitor the Safety of a 200 mg Dose of Bicalutamide in Patients With Advanced Prostate Cancer Summary This is an open label, single-centered treatment protocol designed to monitor the safety of patients treated with a 200 mg daily dose of CASODEX. Patient will receive CASODEX as long as physician feels that he is benefiting from this form of therapy.
View Eligibility Criteria Eligibility Criteria Inclusion Criteria: Histologically or cytologically confirmed adenocarcinoma of the prostate gland Patients with advanced prostate cancer Adult male over the age of 18 years old Normal liver function (AST < 2 x Upper Limit Normal) Exclusion Criteria: ECOG performance status of 4. Previous history or presence of another malignancy other than prostate cancer or treated squamous/basal cell carcinoma of the skin, within the last 5 years.
Check Your Eligibility
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There is 1 Location for this study
Research Site New York New York, , United States
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