Scientists at Minomic International Ltd developed MiCheck™ technology and will present it to international delegates at the American Urology Association, late breaking science plenary session.
The conference will be held in New Orleans from May 15 - 19, 2015. This conference is the largest annual gathering of urologists globally and is expected to draw over 10,000 delegates.
Trial investigator, Dr Jonathan Henderson, will present full data from Minomic's recent pilot study of the MiCheck™ technology on 300 patient samples collected from 10 key urology research centres within the CUSP network, located with geographical diversity throughout the United States.
GPC-1 shows clinical utility in improving specificity of detection for prostate cancer when comparing both prostate cancer patients to those patients who are otherwise healthy or who have documented benign prostatic disease.
Minomic Chief Executive Officer Dr Brad Walsh said the American Urology Association presentation was a critical platform to highlight the company's lead technology, particularly in the high value United States market.
He commented, "This event draws together key opinion leaders in urology from around the world. Presenting our technology at this important showcase is a terrific opportunity. We look forward to presenting full data from the recent successful pilot study, which has shown that MiCheck™ is twice as specific as standard prostate cancer screening technologies."
The MiCheck™ technology is being commercially positioned as an adjunctive test, so it will be used in combination with, rather than a replacement for, existing PSA screening tests.
Dr Shore said he was pleased to continue as principal investigator "A subsequent pivotal trial of the MiCheck™ technology will be launched in the United States later this year, with clinicians/researchers screening 1200 patient samples to provide final stage validation. These results, combined with results from this 300 patient study, will be evaluated and subsequently included in a comprehensive data package submitted to the Food and Drug Administration for regulatory approval."