Prostate Adenocarcinoma Clinical Trial
Official title:
Hedgehog Inhibition as a Non-Castrating Approach to Hormone Sensitive Prostate Cancer: A Phase II Study of Itraconazole in Biochemical Relapse
This phase II trial studies how well itraconazole works in treating patients with biochemically relapsed prostate cancer. Itraconazole may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.
PRIMARY OBJECTIVES:
I. To determine whether the proportion of patients who achieve a >= 50% decline in serum
prostate-specific antigen (PSA) after 12 weeks of protocol therapy with itraconazole dosed at
300 mg orally (PO) twice daily (BID) is superior to a historical control based upon the
observed PSA response proportion in prior studies of non-castrating systemic therapy in men
with biochemically relapsed hormone sensitive prostate cancer.
SECONDARY OBJECTIVES:
I. To determine the median time to PSA progression from the start of protocol therapy with
itraconazole among men with biochemically relapsed prostate cancer.
II. To determine the median time to clinical progression measured from the start of protocol
therapy with itraconazole among men with biochemically relapsed prostate cancer.
III. To determine the median metastasis-free survival measured from the start of protocol
therapy in patients treated with itraconazole for biochemically relapsed prostate cancer.
IV. To determine the mean percent change from baseline after 12 weeks of protocol therapy
compared with pre-treatment in PSA doubling time.
V. To characterize the safety profile of itraconazole in the biochemically relapsed hormone
sensitive prostate cancer population, as graded by Common Toxicity Criteria (CTCAE) version
4.03. All adverse events will be tabulated by grade according to the worst grade experienced.
VI. To determine the mean steady-state itraconazole and hydroxy-itraconazole serum levels
after 4 weeks of therapy with itraconazole.
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