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Clinical Trial Summary

PREVENT is a prospective, multicenter, interventional study evaluating the performance of the OverC multi-cancer detection blood test in asymptomatic individuals with cancer risk.


Clinical Trial Description

Participants will receive the OverC multi-cancer detection blood test along with standard-of-care screening, whose results will be returned to health care providers and participants. The diagnostic procedures will be guided firstly by the OverC multi-cancer detection blood test and then by the standard-of-care screening. The number, cancer types, and cancer clinical stage of cancer patients diagnosed via the OverC multi-cancer detection blood test will be recorded. The study will enroll approximately 12,500 participants as defined by eligibility criteria with an anticipated enrollment period of approximately 9 months at up to 30 clinical sites within China. Participants will be actively followed for approximately 5 years from the date of their enrollment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05227534
Study type Interventional
Source Guangzhou Burning Rock Dx Co., Ltd.
Contact Shangli Cai
Phone 13811823843
Email shangli.cai@brbiotech.com
Status Recruiting
Phase N/A
Start date June 1, 2022
Completion date December 31, 2028

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