A Study of Leuprolide to Treat Prostate Cancer

Inclusion Criteria: * Voluntarily sign an IRB-approved informed consent form and any required privacy statement/authorization form. * Pre-trial serum testosterone level \>150 ng/dL. * Histologically-confirmed prostatic adenocarcinoma in Jewett Clinical Stage A2, B, C or D and TNM\* classification cT1b-4, N: any, M: any. \*Tumor/Nodes/Metastases * Subjects with a rising PSA following radical prostatectomy defined as an increase of 0.2 ng/mL from the previous test on two consecutive testings or rising PSA following prostate irradiation using Phoenix Definition of a rise of greater than or equal to 2.0 ng/mL above the nadir. * Prostate cancer and general clinical status is sufficient to warrant at least 48 weeks of continuous androgen deprivation treatment, without concomitant antiandrogen treatment. * Eastern Cooperative Oncology Group (ECOG) Performance status grades 0,1,or 2 at the time of pre-trial screening. * Life expectancy of at least 18 months. * Subjects with serum creatinine ≤1.9 mg/dL, bilirubin ≤2.0 mg/dL (unless Gilbert's syndrome with normal AST, ALT); AST and ALT ≤2.5 times the upper limit of normal. Exclusion Criteria: * Requires additional treatment including radical prostatectomy, radiotherapy or cryotherapy of local disease. * Historical, clinical, or radiographic evidence of central nervous system metastases, including spinal cord metastasis. * Clinical evidence of urinary tract obstruction. * History of bilateral orchiectomy, adrenalectomy, or hypophysectomy. * History of clinical hypogonadism. * Current malignancy or history of malignancy except for prostate cancer or basal or squamous cell carcinoma of the skin. * Clinical or laboratory evidence of any severe underlying disease state (excluding prostate cancer) that would place subjects in additional jeopardy by participating in this trial. * Hypersensitivity to leuprolide, polylactic acid, or any excipient of the drug. * Incomplete recovery from the effects of any major surgery. * History of receiving of the following prostate cancer therapies within 8 weeks prior to the Screening Visit: chemotherapy, immunotherapy, antiandrogen, radiation therapy, cryotherapy, strontium, or biological response modifiers. * History of prostatic surgery within 4 weeks prior to the Screening Visit. * Received hormonal therapy, including GnRH analogs (less than or equal to 6 month depot administration), estrogen, Megace and phytotherapy, within 32 weeks prior to the Screening Visit and during the trial. * Alternative medical therapies which have an estrogenic, androgenic, or antiandrogenic effect (including phyto-estrogens and phyto-androgens) within 12 weeks prior to the Screening Visit and during the trial. * Requires the chronic use of systemic corticosteroids and anticonvulsants that may affect bone loss such as carbamazepine, phenobarbital, phenytoin, valproic acid or primidone. * May require antiandrogen, immuno-, or surgical therapy for prostate cancer during the trial. * History of alcoholism or consumes \>14 alcoholic beverages per week or illicit drug abuse within 12 months prior to screening. * Received therapy with a GnRH analog (1 year implant) within 60 weeks prior to the Screening Visit. * Received therapy with finasteride or ketoconazole within 1 week prior to the Screening Visit; dutasteride within 25 weeks prior to the Screening Visit.