Inclusion Criteria:

1. Be over 18 years of age

2. Be able to communicate effectively with the study personnel

3. Have histologically confirmed prostate cancer

4. ECOG performance status of 0 to 2

5. Have been treated with ADT(chemical or surgical) for at least 6 months

6. Have castrate level of serum total testosterone (<50 ng/dL)

7. Have a history of serum PSA response after initiation of ADT, serum PSA response is
at least a 90% reduction in serum PSA to <10 ng/mL OR undetectable level of serum PSA
(less tan or =0.2 ng/mL)

8. Have rising serum PSA on two successive assessments at least 2 weeks apart and serum
PSA levels ≥ 2 ng/mL or 2ng/mL and a 25% increase over the nadir after the initiation
of ADT

9. Be continued on androgen deprivation therapy throughout this study

10. Give written informed consent prior to any study specific procedures

11. Subjects must agree to use acceptable methods of contraception:

oIf their female partners are pregnant or lactating acceptable methods of contraception
from the time of the first administration of study medication until 3 months following
administration of the last dose of study medication must be used. Acceptable methods are:
Condom used with spermicidal foam/gel/film/cream/suppository. If the subject has undergone
surgical sterilization (vasectomy with documentation of azospermia) a condom with
spermicidal foam/gel/film/cream/suppository should be used. oIf the male subject's partner
could become pregnant, use acceptable methods of contraception from the time of the first
administration of study medication until 3 months following administration of the last
dose of study medication. Acceptable methods of contraception are as follows: Condom with
spermicidal foam/gel/film/cream/suppository [i.e. barrier method of contraception],
surgical sterilization (vasectomy with documentation of azospermia) and a barrier method
{condom used with spermicidal foam/gel/film/cream/suppository}, the female partner uses
oral contraceptives (combination estrogen/progesterone pills), injectable progesterone or
subdermal implants and a barrier method {condom used with spermicidal
foam/gel/film/cream/suppository}. oIf the female partner has undergone documented tubal
ligation (female sterilization), a barrier method {condom used with spermicidal
foam/gel/film/cream/suppository} should also be used. oIf the female partner has undergone
documented placement of an intrauterine device (IUD) or intrauterine system (IUS) and a
barrier method {condom with spermicidal foam/gel/film/cream/suppository} should also be
used.

Exclusion Criteria:

1. Known hypersensitivity or allergy to estrogen or estrogen like drugs;

2. Have symptomatic metastatic prostate cancer

3. Any disease or condition (medical or surgical) which might compromise the
hematologic, cardiovascular, endocrine, pulmonary, renal, gastrointestinal, hepatic,
or central nervous system; or other conditions that may interfere with the
absorption, distribution, metabolism or excretion of study drug, or would place the
subject at increased risk;

4. History of abnormal blood clotting, Factor V Leiden clotting disorder, thrombotic
disease (venous or arterial thrombotic events such as history of stroke, deep vein
thrombosis (DVT), and/or pulmonary embolus (PE))

5. Symptomatic congestive heart failure (NYHA Class III - IV), unstable angina pectoris,
cardiac arrhythmia

6. The presence of consistently abnormal laboratory values which are considered
clinically significant. In addition, no subject with liver enzymes (ALT or AST) above
2 times the ULN, total bilirubin above 2 times the ULN, or serum creatinine above 1.5
ULN will be admitted to the study

7. Received an investigational drug within a period of 90 days prior to enrollment in
the study

8. Received the study medication previously

9. Currently taking testosterone, testosterone-like agents, or antiandrogens,including
5-alpha reductase inhibitors (may be eligible if allow a 6 week washout period after
stopping antiandrogens);

10. History of prior treatment of cancer chemotherapy agent (other than hormone therapy)
or radiopharmaceutical for prostate cancer.

11. Have taken ketoconazole within the previous 12 months prior to randomization into
this study

12. Have taken diethylstilbestrol or other estrogen products, ketoconazole, or
abiraterone within the previous 12 months prior to randomization into this study

13. Have taken body building or fertility supplements within 4 weeks of admission into
the study

14. Have been previously diagnosed with cancer (other than prostate cancer, superficial
bladder cancer, or non-melanoma skin cancer).