Observational Study for Colorectal Cancer with Minimal Residual Disease

This study is for people with colorectal cancer (CRC) who have minimal residual disease (MRD), meaning a small amount of cancer cells remain after initial treatment. The goal is to see how well biomarker-directed therapies (treatments chosen based on specific features of your cancer, like BRAF or KRAS mutations) help clear these remaining cancer cells, as measured by circulating tumor DNA (ctDNA) in your blood. You would receive treatment decided by your doctor as part of your usual care. Researchers will monitor your progress and collect blood samples every three months to understand how these treatments affect your ctDNA and the chance of your cancer returning. To join, you must be over 18, have a confirmed diagnosis of colorectal adenocarcinoma, and have no clear signs of cancer on scans after initial treatment.

Study design
This is an observational study with 40 planned participants. It is not a randomized trial, meaning treatments are not assigned by the study.
What's involved
You will follow your doctor's treatment plan and provide blood samples every 3 months for correlative studies.
Compensation
Not stated in the trial record.
Follow-up
Your safety and side effects will be monitored through study completion, which is an average of 1 year.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06878131

Precision-MRD: Prospective Observational Study of Biomarker-directed Systemic Therapy for Colorectal Cancer Patients With Minimal Residual Disease

Recruiting
Not specifiedAges 18+Observational
M.D. Anderson Cancer Center
~40 participants
Updated 2026-05-22 on ClinicalTrials.gov
What's tested:Colorectal Cancer

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Safety and Adverse events (AEs)
Measured over Through study completion; an average of 1 year.
Colorectal Cancer

NCT06878131

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • MD Anderson Cancer Center

    Houston, Texasstudy coordinator listed

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

  • Saurav Haldar, MD · PRINCIPAL_INVESTIGATOR · M.D. Anderson Cancer Center

Opens a ready-to-send draft in your own email app — review before sending.

  • Safety and Adverse events (AEs)Through study completion; an average of 1 year.