| Eligibility |
Inclusion Criteria:
1. Age = 18 years.
2. Able to understand and provide a signed informed consent that fulfills the relevant
IRB or Independent Ethics Committee (IEC) guidelines.
3. Histologically-confirmed epithelial ovarian cancer that has progressed on or after SoC
therapy. Germ cell, stromal, and borderline ovarian tumors are not allowed.
4. Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2.
5. Have at least 1 measurable lesion of = 1.5 cm.
6. Must have a tumor biopsy specimen following the conclusion of the most recent
anticancer treatment. If a historic specimen is not available, the subject must be
willing to undergo a biopsy during the screening period.
7. Must be willing to provide blood samples and, if considered safe by the Investigator,
a tumor biopsy specimen at 8 weeks after the start of treatment.
8. Ability to attend required study visits and return for adequate follow-up, as required
by this protocol.
9. Agreement to practice effective contraception for female subjects of child-bearing
potential and non-sterile males. Female subjects of child-bearing potential must agree
to use effective contraception for up to 1 year after completion of therapy, and
non-sterile male subjects must agree to use a condom for up to 4 months after
treatment.
Exclusion Criteria:
1. History of persistent grade 2 or higher (CTCAE Version 4.03) hematologic toxicity
resulting from previous therapy.
2. Within 5 years prior to first dose of study treatment, any evidence of other active
malignancies or brain metastasis except for controlled basal cell carcinoma; prior
history of in situ cancer (eg, breast, melanoma, and cervical); and bulky (= 1.5 cm)
disease with metastasis in the central hilar area of the chest and involving the
pulmonary vasculature.
3. Serious uncontrolled concomitant disease that would contraindicate the use of the
investigational drug used in this study or that would put the subject at high risk for
treatment-related complications.
4. Systemic autoimmune disease (eg, lupus erythematosus, rheumatoid arthritis, Addison's
disease, autoimmune disease associated with lymphoma).
5. History of organ transplant requiring immunosuppression.
6. History of or active inflammatory bowel disease (eg, Crohn's disease, ulcerative
colitis).
7. Requires whole blood transfusion to meet eligibility criteria.
8. Inadequate organ function, evidenced by the following laboratory results:
1. White blood cell (WBC) count < 3,000 cells/mm3
2. Absolute neutrophil count < 1,500 cells/mm3.
3. Platelet count < 100,000 cells/mm3.
4. Hemoglobin < 9 g/dL.
5. Total bilirubin greater than the upper limit of normal (ULN; unless the subject
has documented Gilbert's syndrome).
6. Aspartate aminotransferase (AST [SGOT]) or alanine aminotransferase (ALT [SGPT])
> 2.5 × ULN (> 5 × ULN in subjects with liver metastases).
7. Alkaline phosphatase (ALP) levels > 2.5 × ULN (> 5 × ULN in subjects with liver
metastases, or >10 × ULN in subjects with bone metastases).
8. Serum creatinine > 2.0 mg/dL or 177 µmol/L.
9. International normalized ratio (INR), activated partial thromboplastin time
(aPTT), or partial thromboplastin time (PTT) >1.5 × ULN (unless on therapeutic
anti-coagulation).
9. Uncontrolled hypertension (systolic > 150 mm Hg and/or diastolic > 100 mm Hg) or
clinically significant (ie, active) cardiovascular disease, cerebrovascular
accident/stroke, or myocardial infarction within 6 months prior to first study
medication; unstable angina; congestive heart failure of New York Heart Association
grade 2 or higher; or serious cardiac arrhythmia requiring medication.
10. Dyspnea at rest due to complications of advanced malignancy or other disease requiring
continuous oxygen therapy.
11. Positive results of screening test for human immunodeficiency virus (HIV), hepatitis B
virus (HBV), or hepatitis C virus (HCV).
12. Current chronic daily treatment (continuous for > 3 months) with systemic
corticosteroids (dose equivalent to or greater than 10 mg/day methylprednisolone),
excluding inhaled steroids. Short-term steroid use to prevent IV contrast allergic
reaction or anaphylaxis in subjects who have known contrast allergies is allowed.
13. Known hypersensitivity to any component of the study medication(s).
14. Subjects taking any medication(s) (herbal or prescribed) known to have an adverse drug
reaction with any of the study medications.
15. Concurrent or prior use of a strong cytochrome P450 (CYP)3A4 inhibitor (including
ketoconazole, itraconazole, posaconazole, clarithromycin, indinavir, nefazodone,
nelfinavir, ritonavir, saquinavir, telithromycin, voriconazole, and grapefruit
products) or strong CYP3A4 inducers (including phenytoin, carbamazepine, rifampin,
rifabutin, rifapentin, phenobarbital, and St John's Wort) within 14 days before study
day 1.
16. Concurrent or prior use of a strong CYP2C8 inhibitor (gemfibrozil) or moderate CYP2C8
inducer (rifampin) within 14 days before study day 1.
17. Participation in an investigational drug study or history of receiving any
investigational treatment within 14 days prior to screening for this study.
18. Assessed by the Investigator to be unable or unwilling to comply with the requirements
of the protocol.
19. Concurrent participation in any interventional clinical trial.
20. Pregnant and nursing women.
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