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Recruiting No phase listed Observational

Evaluating Minimal Residual Disease (MRD) Through Longitudinal Circulating Tumor DNA (ctDNA) Profiling in Breast Malignancies

ClinicalTrials.gov ID: NCT07211178

Public ClinicalTrials.gov record NCT07211178. 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 Sep 2, 2026, 2:58 AM EDT

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

Brief summary

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

For patients with breast cancer, it's important to find any remaining cancer cells after they've had their main treatment. Even a few cells, called minimal residual disease (MRD), can lead to the cancer coming back later. A way to find these cells is by looking for tiny bits of cancer DNA that are shed into the blood. This is called circulating tumor DNA (ctDNA). A simple blood test, often called a liquid biopsy, can detect this ctDNA. This research aims to see if finding this cancer DNA in the blood can help predict if a patient's cancer will return. It also may help find out if the treatment is working. Ultimately, the results of this research may help doctors better manage breast cancer and develop new and improved tests and treatments.

Study identification

NCT ID
NCT07211178
Recruitment status
Recruiting
Study type
Observational
Phase
Not listed
Lead sponsor
Tempus AI
Industry
Enrollment
900 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 99 Years
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
Oct 26, 2025
Primary completion
Nov 30, 2032
Completion
Nov 30, 2033
Last update posted
Jun 11, 2026

2025 – 2033

United States locations

U.S. sites
14
U.S. states
13
U.S. cities
14
Facility City State ZIP Site status
Birmingham Hematology Associates Birmingham Alabama 35223 Recruiting
PIH Health Whittier Hospital Whittier California 90602 Recruiting
Cleveland Clinic Florida Weston Florida 33331 Recruiting
Southern Illinois Hospital Services Carbondale Illinois 62902 Recruiting
Cancer Care Specialist of Illinois O'Fallon Illinois 62269 Recruiting
Goshen Center for Cancer Care Goshen Indiana 46526 Recruiting
Trinity Health Ann Arbor Michigan 48106 Recruiting
Oncology Hematology Associates Springfield Missouri 65807 Recruiting
Cancer Care Specialist of Reno Reno Nevada 89511 Recruiting
Summit Medical Group Florham Park New Jersey 07932 Recruiting
University of Cincinnati Medical Center Cincinnati Ohio 45219 Recruiting
Nashville General Nashville Tennessee 37208 Recruiting
Cancer Care Northwest Spokane Valley Washington 99216 Recruiting
Gunderson Health La Crosse Wisconsin 54601 Recruiting

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 NCT07211178, 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 Jun 11, 2026 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07211178 live on ClinicalTrials.gov.

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