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Study identifier: NCT06230185 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

CtDNA Based MRD Testing for NAC Monitoring in TNBC

Condition: TNBC - Triple-Negative Breast Cancer · Minimal Residual Disease  ·  Sponsor: Personalis Inc.

PhaseN/A
Planned participants422
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

A prospective, multicenter, observational study to evaluate the correlation of Molecular Residual Disease (MRD) detection using circulating tumor DNA guided test to pathological complete response (pCR) after neoadjuvant chemotherapy (NAC) in stage I-III triple negative breast cancer (TNBC). Results from this study aim to improve MRD detection and disease outcomes for future patients.

This description comes directly from the study's public registry record.

Talk to the study team

Soumya Chappidi  ·  484-704-2599  ·  schappidi@criteriuminc.com

Julee Hartwell  ·  607-651-6273  ·  jhartwell@criteriuminc.com

Always discuss trial participation with your own doctor first.

Locations (14)

Arizona OncologyTucson, Arizona, United StatesRecruiting
University of Colorado Cancer CenterAurora, Colorado, United StatesRecruiting
George Washington UniversityWashington D.C., District of Columbia, United StatesRecruiting
Mount Sinai Medical Center of FloridaMiami Beach, Florida, United StatesRecruiting
Comprehensive Hematology Oncology (ONare Alliance, LLC / Exigent Research, LLCSt. Petersburg, Florida, United StatesRecruiting
Illinois Cancer CarePeoria, Illinois, United StatesRecruiting
Louisiana State UniversityNew Orleans, Louisiana, United StatesRecruiting
Trinity Health-MichiganYpsilanti, Michigan, United StatesRecruiting
Nebraska MethodistOmaha, Nebraska, United StatesRecruiting
Stony Brook University Cancer CenterStony Brook, New York, United StatesRecruiting
Oregon Oncology SpecialistsSalem, Oregon, United StatesRecruiting
Cancer Care Associates of YorkYork, Pennsylvania, United StatesRecruiting

+ 2 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06230185