๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-08-27

Testing Olaparib Either Alone or in Combination With Atezolizumab in BRCA Mutant Non-HER2-positive Breast Cancer (NCT02849496)

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

๐Ÿ”ต Active, Not Recruiting Phase2 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: National Cancer Institute (NCI)

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

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.

Who can join: Review the eligibility criteria below.

Location: Mayo Clinic Hospital in Arizona โ€” Phoenix, Arizona

Age range: 18 Years

๐Ÿงช Interventions in This Study

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (58 Sites)

Showing the first 25 of 58 sites.

  • Mayo Clinic Hospital in Arizona โ€” Phoenix, Arizona
  • Mayo Clinic in Arizona โ€” Scottsdale, Arizona
  • UC San Diego Moores Cancer Center โ€” La Jolla, California
  • University of California Davis Comprehensive Cancer Center โ€” Sacramento, California
  • UC San Diego Medical Center - Hillcrest โ€” San Diego, California
  • UCSF Medical Center-Mount Zion โ€” San Francisco, California
  • UCHealth University of Colorado Hospital โ€” Aurora, Colorado
  • Smilow Cancer Hospital-Derby Care Center โ€” Derby, Connecticut
  • Smilow Cancer Hospital Care Center-Fairfield โ€” Fairfield, Connecticut
  • Smilow Cancer Hospital Care Center - Guilford โ€” Guilford, Connecticut
  • Smilow Cancer Hospital Care Center at Saint Francis โ€” Hartford, Connecticut
  • Smilow Cancer Center/Yale-New Haven Hospital โ€” New Haven, Connecticut
  • Yale University โ€” New Haven, Connecticut
  • Smilow Cancer Hospital-Orange Care Center โ€” Orange, Connecticut
  • Smilow Cancer Hospital-Torrington Care Center โ€” Torrington, Connecticut
  • Smilow Cancer Hospital Care Center-Trumbull โ€” Trumbull, Connecticut
  • Smilow Cancer Hospital-Waterbury Care Center โ€” Waterbury, Connecticut
  • Mayo Clinic in Florida โ€” Jacksonville, Florida
  • Moffitt Cancer Center-International Plaza โ€” Tampa, Florida
  • Moffitt Cancer Center โ€” Tampa, Florida
  • University of Chicago Comprehensive Cancer Center โ€” Chicago, Illinois
  • UC Comprehensive Cancer Center at Silver Cross โ€” New Lenox, Illinois
  • University of Chicago Medicine-Orland Park โ€” Orland Park, Illinois
  • University of Kansas Clinical Research Center โ€” Fairway, Kansas
  • Johns Hopkins University/Sidney Kimmel Cancer Center โ€” Baltimore, Maryland

๐Ÿ“ž Contact the Study Coordinator

Phone: (800) 664-4580

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—