A Phase II Neoadjuvant Study of Enzalutamide, Abiraterone Acetate, Dutasteride and Degarelix in Men With Localized Prostate Cancer Pre-prostatectomy

Inclusion Criteria:

1. Willing and able to provide written informed consent.

2. Age ≥ 18 years

3. Eastern cooperative group (ECOG) performance status ≤2

4. Documented histologically confirmed adenocarcinoma of the prostate

5. Willing to undergo prostatectomy as primary treatment for localized prostate cancer

6. High risk prostate cancer (per NCCN criteria): Gleason score 8-10 or T3a or PSA > 20
ng/mL -Or- Very-high risk prostate cancer (per NCCN criteria): T3b -T4

7. Serum testosterone ≥150 ng/dL

8. Able to swallow the study drugs whole as tablets

9. Willing to take abiraterone acetate on an empty stomach (no food should be consumed
at least two hours before and for one hour after dosing).

10. Willing to use a condom if having sex with a pregnant woman, or use a condom and
another effective method of birth control if having sex with a woman of child-bearing
potential. These measures are required during and for one week after treatment with
abiraterone.

Exclusion Criteria:

1. Prior local therapy to treat prostate cancer (e.g. radical prostatectomy, radiation
therapy, brachytherapy)

2. Prior use of enzalutamide or abiraterone acetate

3. Prior or ongoing systemic therapy for prostate cancer including, but not limited to:

1. Hormonal therapy (e.g. leuprolide, goserelin, triptorelin, degarelix)

2. CYP-17 inhibitors (e.g. ketoconazole)

3. Antiandrogens (e.g. bicalutamide, nilutamide)

4. Second generation antiandrogens (e.g. enzalutamide, ARN-509)

5. Immunotherapy (e.g. sipuleucel-T, ipilimumab)

6. Chemotherapy (e.g. docetaxel, cabazitaxel)

4. Evidence of serious and/or unstable pre-existing medical, psychiatric or other
condition (including laboratory abnormalities) that could interfere with patient
safety or provision of informed consent to participate in this study.

5. Any psychological, familial, sociological, or geographical condition that could
potentially interfere with compliance with the study protocol and follow-up schedule.

6. Abnormal bone marrow function [absolute neutrophil count (ANC)<1500/mm3, platelet
count <100,000/mm3, hemoglobin <9 g/dL]

7. Abnormal liver function (bilirubin, AST, ALT ≥ 3 x upper limit of normal)

8. Abnormal kidney function (serum creatinine ≥ 2 x upper limit of normal)

9. Abnormal cardiac function as manifested by NYHA (New York Heart Association) class
III or IV heart failure or history of a prior myocardial infarction (MI) within the
last five years prior to enrollment in the study.

10. History of prior cardiac arrhythmia.