RecruitingPhase 2NCT06617858

Trial of AMB-05X for Patients With ctDNA(+) Colorectal Cancer After Curative-intent Treatment

Open-label Phase 2 Trial of AMB-05X for Patients With ctDNA(+) Colorectal Cancer After Curative-intent Treatment


Sponsor

M.D. Anderson Cancer Center

Enrollment

15 participants

Start Date

Dec 4, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

To investigate the efficacy of AMB-05X in patients with CRC with MRD as determined by a ctDNA(+) blood test and no clinically detectable radiographic disease.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This trial is testing AMB-05X — a personalized cancer vaccine — in colorectal cancer patients who have completed curative surgery and treatment but still show a positive ctDNA test. A ctDNA (circulating tumor DNA) test detects tiny fragments of cancer DNA in the blood, even when scans show no visible disease. A positive result after treatment suggests a high risk of the cancer coming back, and this vaccine aims to prevent that recurrence. **You may be eligible if...** - You have been diagnosed with adenocarcinoma of the colon or rectum (stage I–IV) - You have completed all curative-intent treatments and have no visible disease on scans - At least 28 days after finishing all treatments, a ctDNA test (Signatera) came back positive - You are in reasonably good health **You may NOT be eligible if...** - You have visible, measurable cancer remaining after treatment - You have not completed all planned standard treatments - You have significant immune system problems or other serious health conditions Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGAMB-05X

Given by IV


Locations(1)

The University of Texas MD Anderson Cancer Center

Houston, Texas, United States

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NCT06617858


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