Colorectal Cancer and Pre-Cancerous Adenoma Non-Invasive Detection Test Study

Not Applicable

Completed

• Conditions: Colorectal Cancer; Advanced Adenocarcinoma; Serrated Polyp
• Interventions: Diagnostic Test: ColoSense

• Registration Number: NCT04739722
• Lead Sponsor: Geneoscopy, Inc.

Brief Summary

This study was a prospective analysis conducted by Geneoscopy Inc. to evaluate the ColoSense test, which is a multi-target stool RNA test for colorectal cancer screening.

Detailed Description

This phase 3 clinical trial (CRC-PREVENT) was a blinded, prospective, cross-sectional study to support a premarket approval application for a class III medical device. Subjects were recruited onto the clinical trial if they were average-risk subjects, or had a self-reported family history of CRC, aged 45 and older. All participants completed the ColoSense test, which incorporated a commercially available fecal immunochemical test (FIT), concentration of 8 RNA transcripts, and participant-reported smoking status. Stool samples were collected prior to participants completing a colonoscopy at their local endoscopy center. The ColoSense test result (positive or negative) was compared with index lesions observed on colonoscopy. The primary outcomes included ColoSense sensitivity for detecting colorectal cancer, advanced adenomas, or serrated precancerous lesions, and ColoSense specificity for all other findings.

Study Timeline

• Study First Submitted: 2020-09-11
• Study First Submitted QC: 2021-02-03
• Study First Posted: 2021-02-05
• Study Start: 2021-04-12
• Primary Completion: 2022-10-27
• Study Completion: 2024-01-31
• Results First Submitted: 2024-05-31
• Status Verified: 2024-09
• Results First Submitted QC: 2024-09-27
• Last Update Submitted: 2024-09-27
• Results First Posted: 2024-09-30
• Last Update Posted: 2024-09-30

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 14263

Inclusion Criteria

• Subject is male or female, ≥45 years of age
• Subject is able to understand the study procedures, and is able to provide consent to participate in the study and authorizes release of relevant protected health information through reviewing and consenting to a HIPAA medical release form
• Subject is able and willing to provide stool samples within the 120 days prior to a colonoscopy procedure
• Subject is able and willing to undergo a colonoscopy after providing a stool sample

Exclusion Criteria

• Subject had any precancerous finding on most recent colonoscopy. This does not include benign, and/or hyperplastic polyps of any size (Note: Tissue biopsies that result in no histopathology findings are acceptable)

• Subject has a history or diagnosis of colorectal cancer

• Subject has a history of aerodigestive tract cancer

• Subject has had a positive non-invasive screening diagnostic within the associated recommended intervals:

  • Fecal occult blood test or fecal immunochemical test within the previous twelve (12) months
  • FIT-DNA test within the previous 36 months

• Subject has had a colonoscopy in the previous nine (9) years

• Subject has had a prior colorectal resection for any reason other than sigmoid diverticular disease

• Indication for colonoscopy was due to overt rectal bleeding, e.g., hematochezia or melena, within the previous 30 days. (Blood on toilet paper, after wiping, does not constitute rectal bleeding)

• Subject has a diagnosis or personal history of any of the following high-risk conditions for colorectal cancer:

  • Inflammatory bowel disease (IBD) including chronic ulcerative colitis (CUC) and Crohn's disease
  • Familial adenomatous polyposis (also referred to as "FAP", including attenuated FAP)
  • Hereditary non-polyposis colorectal cancer syndrome (also referred to as "HNPCC" of "Lynch Syndrome")
  • Other hereditary cancer syndromes including but are not limited to Peutz-Jeghers Syndrome, MYH-Associated Polyposis (MAP), Gardner's Syndrome, Turcot's (or Crail's) Syndrome, Cowden's Syndrome, Juvenile Polyposis, Cronkhite-Canada Syndrome, Neurofibromatosis and Familial Hyperplastic Polyposis

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
ColoSense	ColoSense	All participants were evaluated with ColoSense prior to undergoing a colonoscopy.

Primary Outcome Measures

Name	Time	Method
ColoSense Sensitivity for Colorectal Cancer (CRC)	120 days from stool sample collection
ColoSense Sensitivity for Advanced Adenoma (AA)	120 days from stool sample collection
ColoSense Sensitivity for Serrated Precancerous Lesions (SPL)	120 days from stool sample collection
ColoSense Specificity for Negative Findings	120 days from stool sample collection

Trial Locations

Locations (2)

Geneoscopy, Inc.; 🇺🇸 Saint Louis, Missouri, United States

Elligo Health Research; 🇺🇸 Austin, Texas, United States