

An FDA Designated Breakthrough Device owned by MiRNA Scientific, Inc. that detects the presence of prostate cancer and accurately assesses the cancer’s aggressiveness using a simple non-invasive urine sample. The Sentinel Test has demonstrated a 97% sensitivity for patients with pathobiological evidence of prostate cancer. The traditional PSA test, MRI, and biopsy combination has just a 44% sensitivity level; making it highly inaccurate, invasive, and potentially leading to impotence, incontinence, infection, and over-treatment.

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