| Eligibility |
Inclusion Criteria:
- Willing and able to provide written informed consent and HIPAA authorization for the
release of personal health information.
NOTE: HIPAA authorization may be either included in the informed consent or obtained
separately.
- Males 18 years of age and above with a life expectancy of at least 6 months.
- Histological or cytological proof of prostate cancer
- Willing to provide a tumor sample via biopsy from a metastatic site of disease to be
collected at screening if safe and feasible per treating investigator discretion.
Adequate archival tissue can be used if available in lieu of baseline biopsy.
- Documented progressive metastatic CRPC based on at least one of the following
criteria:
- Rise in PSA: a minimum of 3 rising levels, with an interval of at least 1 week
between each determination. The last determination must have a value =1 ng/mL,
obtained within 4 weeks of starting study drug
- Measurable disease: new or progressive soft tissue disease on computerized
tomography (CT) or magnetic resonance imaging
- Radionuclide bone scan: at least 2 new bone lesions, as defined by the Prostate
Cancer Clinical Trials Working Group 2 (PCWG2) criteria33
- Serum testosterone < 50 ng/dL. Patients must continue primary androgen deprivation
with an LHRH analogue (agonist or antagonist) if they have not undergone orchiectomy
- ECOG performance status of 0-1
- Finasteride, bicalutamide and nilutamide discontinued at least 4 weeks prior to
registration.
- Physiologic doses of corticosteroids are permitted (i.e., no more than 10mg of
prednisone daily).
- At least 4 weeks must have elapsed from the use of palliative radiation, Strontium-89,
Radium-223, or approved immunotherapy prior to registration.
- Less than or equal to 5 half lives or 4 weeks, whichever is shorter, from the use of
any investigational therapy prior to registration.
- Normal organ function with acceptable initial laboratory values within 14 days of
registration.
- ANC = 1,500/µl
- Hemoglobin = 9g/dL
- Platelet count = 100,000/µl
- Creatinine = 1.5 x the institutional upper limit of normal (ULN), or 24-hr
clearance =50 mL/min
- Potassium = 3.5 mmol/L (within institutional normal range, or correctable with
supplements)
- Bilirubin = 1.5 x ULN (unless documented Gilbert's disease)
- SGOT (AST) = 2.5 x ULN
- SGPT (ALT) = 2.5 x ULN
- Glycated hemoglobin (HbA1c < 6.4%
- Able to take oral medication without crushing, dissolving or chewing tablets.
- Able to adhere to the study visit schedule and other protocol requirements.
Exclusion Criteria:
- Prior exposure to enzalutamide, ARN-509, or other investigational AR-directed therapy
- Prior exposure to abiraterone acetate, ketoconazole or other specific CYP-17
inhibitors
- Prior exposure to agents specifically targeting both mTOR complexes (dual TORC1+TORC2
inhibitors) and/or PI3K/AKT pathways
- Prior chemotherapy for castration resistant disease. Chemotherapy given in the
castration-sensitive setting is permissible. At least 6 months from registration must
have elapsed since chemotherapy was last received.
- Symptomatic central nervous system metastases
- Known history of acute or chronic pancreatitis
- Persistent diarrhea or malabsorption = NCI CTCAE Grade 2, despite medical management
- Clinically significant cardiac diseases, including any of the following:
- Unstable angina pectoris
- Myocardial infarction = 3 months prior to registration
- Other clinically significant heart disease such as congestive heart failure
requiring treatment or uncontrolled hypertension
- Uncontrolled diabetes mellitus
- Other concurrent severe and/or uncontrolled concomitant medical conditions (e.g.,
active or uncontrolled infection) that could cause unacceptable safety risks or
compromise compliance with the protocol
- Major surgery = 2 weeks prior to registration or who have not recovered from side
effects of such therapy. Subjects must have recovered from any effects of recent
radiotherapy that might confound the safety evaluation of study drug.
- Hematopoietic stem cell transplant = 3 months prior to registration.
- Adults of reproductive potential not employing two forms of birth control:
- Males having partners who are female with child-bearing potential must agree that
they and/or their partners will use at least two effective contraceptive methods
(including one barrier method) when engaging in reproductive sexual activity
throughout the study from the time of informed consent, and will avoid conceiving
for 28 days after the last dose of CC-115.
- Known human immunodeficiency virus (HIV) infection
- Known chronic hepatitis B or C virus (HBV/HCV) infection
- Concurrent active second malignancy for which the subject is receiving therapy, other
than non-melanomatous skin cancer or superficial transitional cell carcinoma.
- History of seizure or any condition that may predispose to seizure including, but not
limited to, underlying brain injury, stroke in the past 6 months, primary brain
tumors, brain metastases
- Active treatment with medications that lower the seizure threshold which cannot be
held:
- Aminophylline/theophylline;
- Atypical antipsychotics (e.g., clozapine, olanzapine, risperidone, ziprasidone);
- Bupropion;
- Lithium;
- Pethidine;
- Phenothiazine antipsychotics (e.g., chlorpromazine, mesoridazine, thioridazine);
- Tricyclic and tetracyclic antidepressants (e.g., amitriptyline, desipramine,
doxepin, imipramine, maprotiline, mirtazapine).
- Any other condition which, in the opinion of the Investigator, would preclude
participation in this trial
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