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Active, not recruiting Phase 2 Interventional

Testing Olaparib Either Alone or in Combination With Atezolizumab in BRCA Mutant Non-HER2-positive Breast Cancer

ClinicalTrials.gov ID: NCT02849496

Public ClinicalTrials.gov record NCT02849496. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 1:22 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase II Open-Label, Randomized Study of PARP Inhibition (Olaparib) Either Alone or in Combination With Anti-PD-L1 Therapy (Atezolizumab; MPDL3280A) in Homologous DNA Repair (HDR) Deficient, Locally Advanced or Metastatic Non-HER2-Positive Breast Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This randomized phase II trial studies how well olaparib with or without atezolizumab work in treating patients with non-HER2-positive breast cancer that has spread to nearby tissue or lymph nodes (locally advanced), that cannot be removed by surgery (unresectable), or that has spread from where it first started (primary site) to other places in the body (metastatic). Olaparib is an inhibitor of PARP, an enzyme that helps repair deoxyribonucleic acid (DNA) when it becomes damaged. Blocking PARP may help keep cancer cells from repairing their damaged DNA, causing them to die. PARP inhibitors are a type of targeted therapy. Immunotherapy with monoclonal antibodies, such as atezolizumab, may help the body's immune system attack the tumor, and may interfere with the ability of tumor cells to grow and spread. It is not known whether giving olaparib with or without atezolizumab will work better in patients with non-HER2-positive breast cancer.

Study identification

NCT ID
NCT02849496
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Enrollment
89 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 30, 2017 (Actual)
Primary completion
Jun 10, 2026 (Actual)
Completion
Aug 26, 2027 (Estimated)
Last update posted
Aug 28, 2026

2017 – 2027

United States locations

U.S. sites
58
U.S. states
21
U.S. cities
46
Facility City State ZIP Site status
Mayo Clinic Hospital in Arizona Phoenix Arizona 85054 —
Mayo Clinic in Arizona Scottsdale Arizona 85259 —
UC San Diego Moores Cancer Center La Jolla California 92093 —
University of California Davis Comprehensive Cancer Center Sacramento California 95817 —
UC San Diego Medical Center - Hillcrest San Diego California 92103 —
UCSF Medical Center-Mount Zion San Francisco California 94115 —
UCHealth University of Colorado Hospital Aurora Colorado 80045 —
Smilow Cancer Hospital-Derby Care Center Derby Connecticut 06418 —
Smilow Cancer Hospital Care Center-Fairfield Fairfield Connecticut 06824 —
Smilow Cancer Hospital Care Center - Guilford Guilford Connecticut 06437 —
Smilow Cancer Hospital Care Center at Saint Francis Hartford Connecticut 06105 —
Smilow Cancer Center/Yale-New Haven Hospital New Haven Connecticut 06510 —
Yale University New Haven Connecticut 06520 —
Smilow Cancer Hospital-Orange Care Center Orange Connecticut 06477 —
Smilow Cancer Hospital-Torrington Care Center Torrington Connecticut 06790 —
Smilow Cancer Hospital Care Center-Trumbull Trumbull Connecticut 06611 —
Smilow Cancer Hospital-Waterbury Care Center Waterbury Connecticut 06708 —
Mayo Clinic in Florida Jacksonville Florida 32224-9980 —
Moffitt Cancer Center-International Plaza Tampa Florida 33607 —
Moffitt Cancer Center Tampa Florida 33612 —
University of Chicago Comprehensive Cancer Center Chicago Illinois 60637 —
UC Comprehensive Cancer Center at Silver Cross New Lenox Illinois 60451 —
University of Chicago Medicine-Orland Park Orland Park Illinois 60462 —
University of Kansas Clinical Research Center Fairway Kansas 66205 —
Johns Hopkins University/Sidney Kimmel Cancer Center Baltimore Maryland 21287 —
Massachusetts General Hospital Cancer Center Boston Massachusetts 02114 —
Brigham and Women's Hospital Boston Massachusetts 02115 —
Beth Israel Deaconess Medical Center Boston Massachusetts 02215 —
Dana-Farber Cancer Institute Boston Massachusetts 02215 —
Wayne State University/Karmanos Cancer Institute Detroit Michigan 48201 —
Weisberg Cancer Treatment Center Farmington Hills Michigan 48334 —
Mayo Clinic in Rochester Rochester Minnesota 55905 —
Siteman Cancer Center at Saint Peters Hospital City of Saint Peters Missouri 63376 —
Siteman Cancer Center at West County Hospital Creve Coeur Missouri 63141 —
Washington University School of Medicine St Louis Missouri 63110 —
Siteman Cancer Center-South County St Louis Missouri 63129 —
Siteman Cancer Center at Christian Hospital St Louis Missouri 63136 —
Nebraska Medicine-Bellevue Bellevue Nebraska 68123 —
Nebraska Medicine-Village Pointe Omaha Nebraska 68118 —
University of Nebraska Medical Center Omaha Nebraska 68198 —
Rutgers Cancer Institute of New Jersey New Brunswick New Jersey 08903 —
NYP/Columbia University Medical Center/Herbert Irving Comprehensive Cancer Center New York New York 10032 —
Montefiore Medical Center-Einstein Campus The Bronx New York 10461 —
Montefiore Medical Center-Weiler Hospital The Bronx New York 10461 —
Montefiore Medical Center - Moses Campus The Bronx New York 10467 —
UNC Lineberger Comprehensive Cancer Center Chapel Hill North Carolina 27599 —
Duke University Medical Center Durham North Carolina 27710 —
Case Western Reserve University Cleveland Ohio 44106 —
Ohio State University Comprehensive Cancer Center Columbus Ohio 43210 —
UPMC Hillman Cancer Center Pittsburgh Pennsylvania 15232 —
Vanderbilt Breast Center at One Hundred Oaks Nashville Tennessee 37204 —
Vanderbilt University/Ingram Cancer Center Nashville Tennessee 37232 —
UT Southwestern/Simmons Cancer Center-Dallas Dallas Texas 75390 —
Baylor College of Medicine/Dan L Duncan Comprehensive Cancer Center Houston Texas 77030 —
Farmington Health Center Farmington Utah 84025 —
University of Utah Sugarhouse Health Center Salt Lake City Utah 84106 —
Huntsman Cancer Institute/University of Utah Salt Lake City Utah 84112 —
South Jordan Health Center South Jordan Utah 84009 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02849496, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 28, 2026 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02849496 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →