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Clinical Trial Summary

To evaluate the diagnostic accuracy of the Mitomic Prostate Test (MPT) comparing to prostate biopsy within the intended use population.


Clinical Trial Description

To determine the clinical performance of a blood-based test for clinically significant (CS) prostate cancer (PCa) (grade group ≥ 2) intended for use in men with prostate serum antigen levels in the 'grey zone' (PSA < 10 ng/ml). The test quantifies a previously described 3.4 kb mitochondrial DNA (mtDNA) deletion. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05180305
Study type Observational
Source TSH Biopharm Corporation Limited
Contact Jane Huang
Phone 0226558525
Email [email protected]
Status Recruiting
Phase
Start date April 27, 2021
Completion date December 31, 2022

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