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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03146520
Other study ID # 1-2016-0068
Secondary ID
Status Completed
Phase
First received May 7, 2017
Last updated April 16, 2018
Start date December 13, 2016
Est. completion date March 30, 2018

Study information

Verified date April 2018
Source Genomictree, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Pivotal trials of SDC2 methylation biomarker test in stool DNA to estimate clinical sensitivity and specificity in detection of colorectal cancer.


Description:

The purpose of this study is to validate the clinical performance of EarlyTect Colon Cancer test which is measuring Syndecan 2 methylation status in stool DNA to detect CRC. Syndecan 2 (SDC2) is a newly developed methylation biomarker for colorectal cancer diagnosis. Methylation status of SDC2 gene in stool DNA is determined by methylation specific qPCR. Sensitivity and specificity will be determined by comparing Stool DNA test from healthy subjects, CRC patients, and other group including polyps and other diseases.


Recruitment information / eligibility

Status Completed
Enrollment 634
Est. completion date March 30, 2018
Est. primary completion date March 18, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 30 Years to 80 Years
Eligibility Inclusion criteria:

- sample information is complete, including sample number, gender, family history, stage of cancer, treatment history, and other disease information

- the CRC patient who has not any treatment (surgery, chemotherapy, or radiation)

- non-CRC patient who has not received any treatment (surgery, chemotherapy, or radiation) within the last 6 months

- all of above conditions are satisfied, and any one of below can be applicable; 1) confirm to be CRC with colonoscopy and/or pathological examination, 2) confirm to be inflammatory or ulcerative bowel diseases or benign hyperplastic polyp, 3) confirm to be gastrointestinal or liver cancers who are not CRC, 4) schedule to receive colonoscopy and additional confirmation test for CRC with agreement to provide the test results.

Exclusion criteria: any one of below can be applicable;

- the patient information is not complete and/or does not satisfy inclusion criteria

- the sample information is not complete and/or does not satisfy inclusion criteria

- the CRC patient who has history of colorectal cancer surgery, chemotherapy, or any other treatment

- non-CRC patient who received any chemotherapy within the last 6 months

- the patient who has limited ability or are vulnerable to accept clinical trial agreement

- the patient who is judged as not suitable for clinical trial including a psychiatric disorder by a physician

Study Design


Intervention

Device:
EarlyTect Colon Cancer
SDC2 methylation assay by qPCR using EarlyTect Colon Cancer kit

Locations

Country Name City State
Korea, Republic of Severance Hospital Seoul

Sponsors (2)

Lead Sponsor Collaborator
Genomictree, Inc. Severance Hospital

Country where clinical trial is conducted

Korea, Republic of, 

References & Publications (1)

Oh T, Kim N, Moon Y, Kim MS, Hoehn BD, Park CH, Kim TS, Kim NK, Chung HC, An S. Genome-wide identification and validation of a novel methylation biomarker, SDC2, for blood-based detection of colorectal cancer. J Mol Diagn. 2013 Jul;15(4):498-507. doi: 10.1016/j.jmoldx.2013.03.004. Epub 2013 Jun 7. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical performance of EarlyTect Colon Cancer to detect colorectal cancer Sensitivity and specificity of EarlyTect Colon Cancer to detect colorectal cancer (sensitivity: the ratio of positive cases in all CRC cases, specificity: the ratio of negative cases in all healthy controls) 1.5 years
Secondary Positive ratio of SDC2 methylation in polyps the ratio of SDC2 methylation positive in polyps 1.5 years
Secondary Positive ratio of SDC2 methylation in other cancers the ratio of SDC2 methylation positive in other cancers 1.5 years
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