500
Participants
Start Date
January 31, 2016
Primary Completion Date
January 1, 2020
Study Completion Date
January 1, 2020
blood draw
Participants will have a venous blood draw of \~20mLs before prostate biopsy. The biopsy will then be performed and histologically graded for any malignancy present. This grade will be statistically analyzed with respect to the Copy Number Instability (CNI) determined from the results of the molecular examination of the cell-free DNA in the blood.
University of Maryland Cancer Center, Baltimore
Vanderbilt University Medical Center, Nashville
Lead Sponsor
Smerud Medical Research International AS
OTHER
Vanderbilt University
OTHER
Chronix Biomedical Corporation
INDUSTRY