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Active, Not Recruiting

NCT Number: NCT06398743

First CORRECT Study of Minimal Residual Disease (MRD) Detection in Colorectal Cancer

The CORRECT - MRD I study will prospectively enroll patients who have undergone complete surgical resection for stage II or III colorectal cancer. Patients will be followed for up to 5 years for recurrence.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Tel Aviv Sourasky Medical Center, Tel Aviv Yaffo, Central District, Israel

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Subject is/has:

  • 18 years of age or older.
  • Diagnosis of carcinoma of the colon or rectum (patients with lymphomatous, sarcomatous,or neuroendocrine features are not eligible).
  • Post complete surgical resection of CRC, with last surgery occurring within 180 days prior to enrollment are eligible if all of the following conditions are met:
  • in the opinion of the surgeon, all grossly visible tumor was completely resected ("curative resection") and
  • histologic evaluation by the pathologist confirms the margins of the resected specimens are not involved by malignant cells.

i. Patients with T4 tumors that have involved an adjacent structure (e.g., bladder, small intestine, ovary, etc.) by direct extension form the primary tumor must have had all or a portion of the adjacent structure removed en bloc with the primary tumor and local radiation therapy will not be utilized.

  • Pathologic Stage II or III CRC.
  • ECOG performance status ≤ 2 (0, 1 or 2).
  • Able to understand and provide written informed consent.
  • Willing and able to comply with the study requirements, which includes the collection of approximately 35mL of blood for each research blood draw.

Exclusion criteria

Subject is/has:

  • Initiated adjuvant therapy for current CRC diagnosis (note: neoadjuvant therapy acceptable).
  • Known pregnancy or breastfeeding at time of enrollment.
  • Prior history of any invasive cancer (including CRC) within the past 3 years prior to informed consent, with the exception of non-melanoma skin cancer. Patients with a prior history of noninvasive (in situ) carcinomas may participate after definitive treatment.
  • Prior transplant history:
  • Prior allogeneic hematopoietic stem cell transplant at any time.
  • Prior solid organ transplant within the last 2 years prior to enrollment.
  • Multiple cancer diagnoses: Synchronous or asynchronous diagnoses (or suspicion) of multiple primary cancers at the time of eligibility screening.

Treatment and study plan

MRD

Device

ctDNA MRD test

Primary outcomes

  1. To validate the association of post-definitive therapy and pre-recurrence follow-up ctDNA positivity with Recurrence Free Interval, defined as elapsed time from surgical resection to the first clinical recurrence or CRC-related death.

    Time frame: 6 years

Secondary outcomes

  1. Time from the first ctDNA positivity to recurrence among subjects who have a positive ctDNA finding and have recurred.

    Time frame: 6 years

Sponsors and collaborators

Lead sponsor

Exact Sciences Corporation

Industry

Collaborators

  • Fortrea

Registry information

Official study title

CORRECT-MRD I: First Colorectal Cancer Clinical Validation Study to Predict Recurrence Using a Circulating Tumor DNA Assay to Detect Minimal Residual Disease

Acronym: MRD

Important dates

Study start
2023
Primary completion
2027
Study completion
2027
First posted
May 3, 2024
Registry last updated
Jul 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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