Niraparib in Combination With Pembrolizumab in Patients With Triple-negative Breast Cancer or Ovarian Cancer



Status:Active, not recruiting
Conditions:Breast Cancer, Ovarian Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:2/14/2018
Start Date:March 2016
End Date:February 2019

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Phase 1/2 Clinical Study of Niraparib in Combination With Pembrolizumab (MK-3475) in Patients With Advanced or Metastatic Triple-Negative Breast Cancer and in Patients With Recurrent Ovarian Cancer

This Phase 1/2 study will evaluate the safety and efficacy of combination treatment with
niraparib and pembrolizumab (MK-3475) in patients with advanced or metastatic triple-negative
breast cancer or recurrent ovarian cancer. (KEYNOTE-162)


Main Inclusion Criteria:

- Patient has histologically proven advanced (unresectable) or metastatic cancer as
outlined below according to study phase and disease type:

1. Phase 1 patients (breast or ovarian cancer)

- Patients with advanced or metastatic breast cancer must have disease that is
HER2-negative, estrogen receptor-negative, and progesterone
receptor-negative (ie, TNBC). Patients with advanced or metastatic disease
may have up to 4 lines of cytotoxic therapy. Neoadjuvant and adjuvant
therapies are not counted towards lines of therapy.

- Patients must have any epithelial (ie, serous, endometroid, mucinous, clear
cell) ovarian, fallopian tube, or primary peritoneal cancer. Patients must
have experienced a response lasting at least 6 months to first-line
platinum-based therapy but currently considered to have platinum-resistant
disease per investigator's assessment (e.g, patient is not eligible for
further platinum containing treatment). Patients may have received up to 5
lines of cytotoxic therapy for advanced or metastatic cancer. Neoadjuvant
and adjuvant therapies are not counted towards lines of therapy.

2. Phase 2 patients (breast or ovarian cancer)

- Patients with advanced or metastatic breast cancer must have TNBC. Patients
with advanced or metastatic disease may have received up to 2 lines of
cytotoxic therapy. Adjuvant and/or neoadjuvant therapies are not counted in
the number of lines of therapy. TNBC patients who have previously received
platinum chemotherapy in the metastatic setting are allowed to enroll in the
study as long as they did not progress while on or within 8 weeks from the
day of the last platinum administration.

- Patients must have with high-grade serous or endometroid ovarian, fallopian
tube, or primary peritoneal cancer. Patients must have experienced a
response lasting at least 6 months to first-line platinum-based therapy but
currently considered to have platinum-resistant disease per investigator's
assessment (e.g, patient is not eligible for further platinum containing
treatment). Patients may have had up to 4 lines of cytotoxic therapy for
advanced or metastatic cancer. Neoadjuvant, adjuvant, and the combination of
both will be considered as one line of therapy.

- Archival tumor tissue available or a fresh biopsy must be obtained prior to study
treatment initiation

- Measurable lesions by RECIST v1.1

- Eastern Cooperative Oncology Group (ECOG) 0 or 1

- Adequate organ function

- Able to take oral medications

- Female patient, if of childbearing potential, has a negative serum pregnancy test
within 72 hours of taking study medication and agrees to abstain from activities that
could result in pregnancy from enrollment through 120 days after the last dose of
study treatment

- Male patient agrees to use an adequate method of contraception

Main Exclusion Criteria:

- Patients with primary platinum refractory ovarian cancer (ie, progressive disease on
or within 6 months of first-line platinum therapy)

- Known active central nervous system (CNS) metastases and/or carcinomatous meningitis
Note: Patients previously treated for brain metastases may be able to participate
provided they are stable

- Patient has a known additional malignancy that progressed or required active treatment
within the last 2 years. Exceptions include basal cell carcinoma of the skin, squamous
cell carcinoma of the skin that has undergone potentially curative therapy, or in situ
cervical cancer

- Poor medical risk

- Condition (such as transfusion dependent anemia or thrombocytopenia), therapy, or
laboratory abnormality that might confound the study results, or interfere with the
patient's participation for the full duration of the study treatment.

- Pregnant or breastfeeding, or expecting to conceive children within the projected
duration of the study

- Immunodeficiency or is receiving systemic steroid therapy or any other form of
immunosuppressive therapy within 7 days prior to the first dose of study treatment

- Known history of human immunodeficiency virus (HIV) (HIV 1/2 antibodies)

- Known active hepatitis B or hepatitis C

- Active autoimmune disease that has required systemic treatment in the past 2 years
(ie, with use of disease-modifying agents, corticosteroids, or immunosuppressive
drugs). Replacement therapy (eg, thyroxine, insulin, or physiologic corticosteroid
replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a
form of systemic treatment

- Prior treatment with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent

- Prior treatment with a known poly(ADP-ribose) polymerase (PARP) inhibitor

- Heart-rate corrected QT interval (QTc) prolongation > 470 msec at screening

- Known history or current diagnosis of myelodysplastic syndrome (MDS) or acute myeloid
leukemia (AML)
We found this trial at
28
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Chapel Hill, North Carolina
Phone: 919-843-5963
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Birmingham, Alabama
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Boston, Massachusetts
Phone: 617-632-2334
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Burlington, Massachusetts
Phone: 781-744-3071
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Charlotte, North Carolina 28207
Phone: 980-442-9431
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Charlottesville, Virginia
Phone: 434-297-7782
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Chicago, Illinois
Phone: 773-702-3112
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Cleveland, Ohio
Phone: 800-641-2422
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Covington, Louisiana 70433
Phone: 985-893-0911
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Detroit, Michigan
Phone: 313-576-9717
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Jacksonville, Florida 32209
Phone: 904-953-7755
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Lake Success, New York 11042
Phone: 516-734-8248
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Los Angeles, CA
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Memphis, Tennessee
Phone: 901-322-0251
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Miami, FL
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Morristown, New Jersey 07960
Phone: 973-971-6284
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Nashville, Tennessee 37232
Phone: 615-329-7437
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New York, New York 10032
Phone: 212-746-2071
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Oklahoma City, Oklahoma
Phone: 405-271-8777
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Orlando, Florida 32804
Phone: 407-303-7101
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Rochester, Minnesota 55905
Phone: 507-284-2511
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San Antonio, Texas 78224
Phone: 210-450-1366
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San Francisco, California
Phone: 415-353-4084
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Scottsdale, Arizona
Phone: 480-323-1339
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Seattle, Washington 98105
Phone: 206-288-6440
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