Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
GTx
Age
18–any
Sex
MALE
Healthy volunteers
Not accepted
You may be eligible if
Be over age 18 years
Be able to Communicate effectively with the study personnel
Have histologically confirmed prostate cancer
Have castration resistant prostate cancer patients with radiographic evidence of metastatic disease (T any - N any - MI)
ECOG performance status of 0 to 2
Have been treated with ADT (chemical or surgical) for at least 6 months
Have a castrate level of serum total testosterone (\< 50ng/dL)
Have a history of serum PSA response on ADT. A serum PSA response is an undetectable level of serum PSA (≤ 0.2/mL) or at least a 90% reduction in serum PSA from the serum PSA value prior to the initiation of treatment to \< 10ng/mL
Have a rising serum PSA on two successive assessments at least 2 weeks apart and serum PSA levels ≥ 2ng/mL or \> 2 ng/mL and a 25% increase above the nadir from the ADT.
Be continued on ADT throughout this study
give written informed consent prior to any study specific procedures
subjects must agree, if not already on anticoagulation therapy or aspirin, to take 81 mg aspirin daily throughout the duration of their participation in this study and for 30 days after completion of dosing with GTx-758.
Subjects must agree to use acceptable methods of contraception:
If 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.
If 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/fil/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}.
If the female partner has undergone documented tubal ligation (female sterilization), a barrier method {condom used with spermicidal foam/gel/film/cream/suppository} should be used
If the female partner has undergone documented placement of an intrauterine device (IUD) or intrauterine system (IUS), a barrier method {condom with spermicidal foam/gel/film/cream/suppository} should also be used.
Have previously taken or are currently taking diethylstilbestrol, other estrogens, abiraterone or ketoconazole or any other inhibitor of CYP17 (17a-hydroxylase/C17,20-lyase);
Currently having radiation therapy to prostate for cancer control (radiation to bone to relieve pain is acceptable)
Have previously taken or are currently taking enzalutamide;
Have previously received cytotoxic chemotherapy for prostate cancer;
Recent hospitalization (within 30 days of screening);
Recent surgery (within 30 days of screening);
Have taken body building or fertility supplements within 4 weeks of admission into the study;
Have been previously diagnosed or treated for active cancer (other than prostate cancer or non-melanoma skin cancer)within the previous five years;
Have a BMI \> 35.
You may not be if
Known hypersensitivity or allergy to estrogen or estrogen like drugs
Need for urgent chemotherapy, radiation therapy or surgical intervention for prostate cancer in the opinion of the investigator;
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
Subjects with a personal history of abnormal blood clotting or thrombotic disease (venous or arterial thrombotic events such as history of stroke, deep vein thrombosis (DVT), and or pulmonary embolus (PE)).
Any subjects, as determined by a central laboratory, with
1. a modified activated protein C reaction ratio ≤ 2.5 and a Factor V Leiden gene mutation,
2. an antithrombin level below the lower limit of the normal range,
3. an antiphospholipid antibody level that is indeterminate, positive, or outside the normal range,
4. or a prothrombin gene mutation
Symptomatic congestive heart failure (NYHA Class III - IV), unstable angina pectoris, cardiac arrhythmia, or history of atrial fibrillation
The presence of consistently abnormal laboratory values which are considered clinically significant. In addition, any subject with liver enzymes (ALT or AST) above 2 times the upper limit of normal, total bilirubin above 2 times the upper limit of normal, or serum creatinine above 1.5 times the upper limit of normal will NOT be admitted to the study.
Received an investigational drug within a period of 90 days prior to the enrollment in the study.
Received the study medication GTx-758 previously;
Clareo Health | Study of the Effect of GTx-758 on Serum PSA and Testosterone in Men With Prostate Cancer
