| Eligibility |
Inclusion Criteria:
1. Subjects with CA125-associated recurrent epithelial adenocarcinoma of ovarian,
fallopian tube or peritoneal origin.
2. Subjects must have histologically diagnosed high-grade (Grade 2 or 3) serous
epithelial ovarian, fallopian tube, or primary peritoneal cancer with recurrent
disease and must have been previously treated with chemotherapy and experienced a
response lasting at least 6 months to first-line platinum-based therapy.
3. Previously treated disease with up to 3 prior lines of therapy, including at least one
platinum-based therapy. Each line of therapy should have been changed due to
recurrence, progression, or toxicity. Maintenance therapy with bevacizumab, hormonal
therapies and / or a PARP inhibitor is not considered a line of therapy.
4. Must have received prior platinum-based chemotherapy for first line ovarian cancer,
however they must have been platinum sensitive for =6 months after the most recent
platinum-containing regimen prior to the start of study treatment.
5. Must have medical assessment consistent with prognosis for an expected survival of at
least 6 months and be clinically appropriate to receive a 12-week hiatus from any
cytotoxic treatment according to the best clinical judgement of the treating
Investigator.
6. Must have had an elevated serum CA125 >50 units / mL measured at screening within 28
days of start of study treatment.
7. Must have measurable disease, including identification of marker lesions, by
radiographic or physical criteria suitable for evaluation according to RECIST v1.1 for
documentation of disease response or progression.
8. Must have an ECOG Performance Status of 0, 1 or 2.
9. Must have adequate organ function defined as:
1. Absolute neutrophil count =1,500 / µL
2. Platelets =100,000 / µL
3. Hemoglobin =9 g / dL
4. Total bilirubin =1.5 x ULN (=2.0 x ULN in subjects with known Gilberts syndrome)
OR direct bilirubin =1 x ULN
5. LDH, SGOT and SGPT<2.5 x ULN
6. Albumin >3.5 g / dL
7. Serum Creatinine < 1.5 mg/dL
10. For women of childbearing potential, a negative pregnancy test and willingness to
avoid pregnancy by using a highly effective method of contraception from the first
dose of study treatment to 6 months after last dose of study treatment.
11. Able to take oral medications.
12. Sign informed consent and authorization permitting release of personal health
information.
Exclusion Criteria:
1. Subject must not be simultaneously treated in any interventional clinical trial.
2. Subject must not have had major surgery =3 weeks prior to initiating protocol therapy
and subject must have recovered from any surgical effects.
3. Subject must not have received investigational therapy =4 weeks, or within a time
interval less than at least 5 half-lives of the investigational agent, whichever is
shorter, prior to initiating protocol therapy.
4. Subject has had radiation therapy encompassing >20% of the bone marrow within 2 weeks;
5. Subject must not have received a transfusion (platelets or red blood cells) =2 weeks
prior to first dose of study treatment.
6. Subject must not have received colony-stimulating factors (e.g., granulocyte
colony-stimulating factor, granulocyte macrophage colony-stimulating factor, or
recombinant erythropoietin) within 4 weeks prior to initiating protocol therapy.
7. Subject has had any known Grade 3 or 4 anemia, neutropenia or thrombocytopenia due to
prior chemotherapy that persisted >4 weeks and was related to the most recent
treatment.
8. Subject must not have a serious, uncontrolled medical disorder, nonmalignant systemic
disease, or active, uncontrolled infection or active infection causing fever. Examples
include, but are not limited to, uncontrolled major seizure disorder, unstable spinal
cord compression, superior vena cava syndrome, or any psychiatric disorder that
prohibits obtaining informed consent. Subjects with chronic diseases that are well
controlled (e.g., diabetes mellitus, hypertension [<140 sBP and <90 dBP]) are
eligible.
9. Evidence of clinically significant cardiovascular and respiratory conditions including
myocardial infarction within 1 year, uncontrolled or unstable angina, congestive heart
failure (New York Heart Association Class III or IV), arrhythmia (Grade 2 or higher),
chronic obstructive pulmonary disease, persistent asthma, or a history of asthma
within 5 years.
10. Subject must not have any known history of myelodysplastic syndrome (MDS) or acute
myeloid leukemia (AML)
11. Diagnosed or treated for another malignancy within 5 years before the first dose, or
previously diagnosed with another malignancy and have any evidence of residual
disease. Subjects with non-melanoma skin cancer or cervix carcinoma in situ are not
excluded if they have undergone complete resection.
12. Subject must not have known, symptomatic brain or leptomeningeal metastases.
13. Have an active autoimmune disease (e.g., rheumatoid arthritis, SLE, ulcerative
colitis, Crohn's Disease, MS, ankylosing spondylitis, thyroiditis) requiring
continuing immune suppressive therapy.
14. Recognized immunodeficiency condition including cellular immunodeficiencies,
hypogammaglobulinemia or dysgammaglobulinemia; subjects who have hereditary, or
congenital immunodeficiency's (HIV infection, see below).
15. Chronically treated with systemic doses of immunosuppressive drugs such as
cyclosporine, methotrexate, adrenocorticotropic hormone (ACTH) or immune suppressive
monoclonal antibodies.
16. Chronic therapeutic corticosteroid use, defined as >5 days of prednisone or
equivalent, with the exception of inhalers or those on a pre-planned steroid taper.
(Note: Premedication with corticosteroids per institutional standard of care is
allowed).
17. Any previous treatments with oregovomab.
18. Known allergy to murine proteins or hypersensitivity to oregovomab, niraparib, or any
of the excipients of oregovomab or niraparib.
19. Have contraindications to the use of pressor agents (e.g., SC epinephrine), notably
monoamine oxidase inhibitor (MAOI) use.
20. Any of the following conditions (on-study testing is not required):
1. Known HIV-infected subjects unless on effective anti-retroviral therapy with an
undetectable viral load within 6 months, or
2. Known or suspected hepatitis B if active infection (subjects with chronic
hepatitis B infection must have an undetectable HBV viral load on suppressive
therapy, if indicated; positive surface antibody alone is not an exclusion), or
3. Known or suspected hepatitis C infection which has not been treated and cured
unless currently on treatment with an undetectable viral load).
21. Unable understand, and / or unwilling to sign a written consent form which must be
obtained prior to treatment.
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