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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00696345
Other study ID # Septin-9-2006
Secondary ID
Status Completed
Phase N/A
First received June 10, 2008
Last updated June 13, 2008
Start date January 2005
Est. completion date February 2007

Study information

Verified date June 2008
Source Epigenomics, Inc
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review BoardGermany: Ethics Commission
Study type Observational

Clinical Trial Summary

Epigenomics is developing a colon cancer screening assay based on differential methylation of specific CpG sites for the detection of early stage disease. A genome-wide methylation analysis and oligonucleotide array study using DNA from various stages of colon cancer and normal tissue have been completed to obtain candidate CpG markers. Based on results obtained in the above studies, Epigenomics has moved to the final stages of feasibility with a specific, highly sensitive real-time marker assay that is able to detect colon cancer DNA in blood plasma.


Description:

From public health as well as health economics perspectives, the poor adoption of current screening options limits the effectiveness of CRC screening initiatives; as stated by Sidney Winawer, MD, "the best test is the one that gets done." Current CRC screening guidelines include FOBT, sigmoidoscopy (alone or with FOBT), or colonoscopy. Non-invasive screening is conducted using FOBT, which while inexpensive, exhibits a low compliance rate (around 16% in the US) due to its use restrictions, perceived inconvenience and lack of consumer acceptance. The gold standard procedure for CRC detection is colonoscopy; it exhibits excellent performance characteristics, but has a limited utility as a first line screen due to its high cost, healthcare delivery resource limitations, and inadequate patient acceptance. It is believed a noninvasive, first-line screening assay capable of detecting individuals with colorectal disease, confirmed by colonoscopy, would have greater utility for population screening.

Epigenomics has identified methylated gene regions that are specific for colorectal cancer or pre-malignant tissue. Aberrantly methylated genes represent attractive candidate markers for cancer screening, as cancer-specific methylation changes occur early in tumorigenesis, appear to be stable, yield a positive amplifiable signal, and can be assayed with high analytical sensitivity. Since methylation occurs early and in distinct genomic areas, it is possible to achieve high clinical sensitivity with a small number of methylated DNA markers. Studies have shown that aberrantly methylated DNA markers can be detected in tissue and body fluids and are highly correlated to colorectal cancer.


Recruitment information / eligibility

Status Completed
Enrollment 700
Est. completion date February 2007
Est. primary completion date October 2006
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 40 Years and older
Eligibility Inclusion Criteria:

- Group 1 diagnosis of colorectal cancer

Exclusion Criteria:

- Group 2 diagnosis of colorectal cancer

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Germany Department of Surgery and Surgical Oncology, Charité Campus Berlin Buch Berlin
Germany Department of Visceral-, Thoracic- and Vascular Surgery, University Hospital Carl Gustav Carus Dresden
Germany Department of Surgery, University Hospital Schleswig-Holstein, Campus Lübeck Lübeck
Germany Völklingen Clinic Völklingen
Hungary Semmelweis University Budapest

Sponsors (1)

Lead Sponsor Collaborator
Epigenomics, Inc

Countries where clinical trial is conducted

Germany,  Hungary, 

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