Phase 2 Study of Abarelix in Androgen-Independent Prostate Cancer Progressing After Agonist Therapy

Inclusion Criteria:

- Signed informed consent

- Histologically or cytologically confirmed prostate cancer that has progressed within
60 days of the start of screening despite castrate levels of testosterone from
treatment with an LHRH agonist. Progression will be defined as one or more of the
following: *A rising PSA, defined as at least two consecutive rises in PSA over a
reference value (PSA #1). The first rising PSA (PSA #2) must be taken at least one
week after PSA #1. A third PSA (PSA #3) is required to be greater than PSA #2; if
not, a fourth PSA (PSA #4) is required to be greater than PSA #2, OR

- The appearance of new metastatic lesions on a bone scan, OR

- Progression of known lesions or the appearance of new metastatic lesions on CT,
MRI, chest x-ray, or other radiographic evaluations.

- Subject whose hormonal therapy includes an anti-androgen must have the anti-androgen
discontinued prior to the start of screening (at least 6 weeks for bicalutamide and
at least 4 weeks otherwise). If there is a reduction in the PSA after anti-androgen
withdrawal, the subject must continue to demonstrate progression as defined above
after anti- androgen withdrawal to be eligible.

- ECOG Performance Status ≤ 3

- Age ≥ 18 years of age

- Life expectancy ≥ 6 months

- Serum testosterone less than or equal to 50 ng/dL

- PSA ≥ 5 ng/mL (if progression is determined from a rise in PSA)

- WBC greater than or equal to 3,000/mm3

- Hematocrit ≥ 30%

- Platelet count greater than or equal to 100,000/mm3

- Serum creatinine less than or equal to 2 x upper limit of normal (ULN)

- Bilirubin (direct or total) less than or equal to 2 x ULN

- SGPT (ALT) and SGOT (AST) less than or equal to 2 x ULN

Exclusion Criteria:

A subject is ineligible to participate in the study if he meets any of the following
criteria:

- Prior treatment for prostate cancer with:

- Chemotherapy

- Radiopharmaceutical such as strontium or samarium

- Diethylstilbesterol or another estrogen agonist or antagonist

- Ketoconazole

- Aminoglutethimide

- Current treatment with Class IA (e.g., quinidine, procainamide) or Class III (e.g.,
amiodarone, sotalol) antiarrhythmic medication

- Currently taking PC SPES

- History of allergy to a LHRH agonist or GnRH antagonist

- Major surgery within 4 weeks

- Serious medical illnesses, including malnutrition, that in the judgment of the
investigator would preclude protocol treatment

- Significant cardiovascular illness defined as NYHA class III or IV congestive heart
failure or unstable angina within 6 months, myocardial infarction within 12 months,
deep venous thrombosis within 2 years, or any history of acute pulmonary embolism

- Active second malignancy other than non-melanoma skin cancer or superficial bladder
cancer

- Any uncontrolled infection, including HIV

- Any other experimental therapy within 4 weeks prior to study entry

- QTc > 450 msec on a screening ECG obtained by the investigator