PROSPER: This phase III study is assessing the safety and effect of enzalutamide (an oral drug) in patients with non metastatic prostate cancerA Multinational, Phase 3, Randomized, Double Blind, Placebo Controlled, Efficacy and Safety Study of Enzalutamide in Patients With Nonmetastatic Castration Resistant Prostate Cancer (Other ID's: MDV3100-14, CT622)

Exclusion

• Prior cytotoxic chemotherapy;
• Use of hormonal therapy or biologic therapy for prostate cancer (other than approved bone targeting agents and GnRH agonist/antagonist therapy) or use of an investigational agent within 4 weeks of randomization;
• Known or suspected brain metastasis or active leptomeningeal disease;
• History of another invasive cancer within 3 years of randomization;
• Absolute neutrophil count < 1000/μL, platelet count < 100,000/μL, or hemoglobin < 10 g/dL (6.2 mmol/L) at screening;
• Total bilirubin ≥ 1.5 times the upper limit of normal;
• Creatinine > 2 mg/dL (177 µmol/L) at screening;
• Albumin < 3.0 g/dL (30 g/L) at screening;
• History of seizure or any condition that may predispose to seizure;
• Clinically significant cardiovascular disease;
• Gastrointestinal disorder affecting absorption;
• Major surgery within 4 weeks of randomization;
• Hypersensitivity reaction to the active pharmaceutical ingredient or any of the capsule components, including Labrasol, butylated hydroxyanisole, and butylated hydroxytoluene;
• Any concurrent disease, infection, or comorbid condition that interferes with the ability of the patient to participate in the trial, which places the patient at undue risk, or complicates the interpretation of data, in the opinion of the investigator or medical monitor.