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LexaGene to Place Beta Unit in Human Clinical Diagnostics Laboratory

LexaGene to Place Beta Unit in Human Clinical Diagnostics Laboratory

Assurance Scientific Laboratories to explore open-access use for antimicrobial resistance research

BEVERLY, Mass., Aug. 08, 2019 (GLOBE NEWSWIRE) -- , (; ) (the “Company”), a biotechnology company that develops genetic analyzers for rapid pathogen detection and other molecular markers, announced today it has an agreement to place a beta prototype with (ASL) in Vestavia, Alabama in August 2019. ASL is a certified reference laboratory specializing in providing clinical testing results to physicians nationwide. 

ASL currently processes over 300 urine samples per week for human urinary tract infections – plus hundreds of other sample types. The beta test will focus on testing urine samples to detect the presence of pathogens causing urinary tract infections while simultaneously screening these samples for genetic markers for antimicrobial resistance. ASL has expertise in developing and testing for antimicrobial resistance genes using PCR-based tests. Antimicrobial resistance – the resistance of bacteria, fungus, and viruses to drugs – is a worldwide problem that .1

Dr. Nathan Walsh, LexaGene’s VP of Applications and Bio-Informatics states, “During this beta test period, ASL will take advantage of the open-access feature of LexaGene’s LX technology to compare our tests to their tests for pathogen identification and antimicrobial resistance characterization. The research data generated will help clinical laboratories better assess the available tools to aid in the diagnosis and treatment of human urinary tract infections.”

At ASL, Mary Beth Minyard, Director of Microbiology, and Dr. Greer Massey, Director of Molecular Diagnostics, will lead the project. “We are always looking for new technology to help us streamline sample processing and analysis. We are excited to evaluate LexaGene’s LX technology, especially for its integrated sample extraction, test assembly, and analysis which has the potential to expedite sample processing in the lab, lower costs and minimize errors,” states Massey.

Dr. Jack Regan, CEO and Founder of LexaGene states, “Our open-access technology differentiates us from other automated molecular testing technologies.  This collaborative effort with ASL, a reference laboratory that processes human samples for clinical diagnostic testing, is a perfect example of a laboratory taking advantage of the open-access feature to test the performance of their own assays on our fully automated analyzer. We are excited to have this opportunity to demonstrate the instrument’s capabilities, and how it may someday be used for human clinical diagnostics.”

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About LexaGene Holdings Inc.

LexaGene is a biotechnology company that develops genetic analyzers for pathogen detection and other molecular markers for on-site rapid testing in veterinary diagnostics, food safety and for use in open-access markets such as clinical research, agricultural testing and biodefense. End-users simply need to collect a sample, load it onto the instrument with a sample preparation cartridge, enter sample ID and press ‘go’. The LX Analyzer delivers excellent sensitivity, specificity, and breadth of detection and can process multiple samples at a time, in an on-demand fashion, returning results in about 1 hour. The unique open-access feature is designed for custom testing so that end-users can load their own real-time PCR assays onto the instrument to target any genetic target of interest.

About Assurance Scientific Laboratories

Assurance Scientific Laboratories (ASL) is comprised of a passionate team of medical doctors and scientists who believe in using the best objective data available to help health care providers make accurate and timely diagnoses. Our mission is to provide healthcare providers with Assurance to treat their patients in the best manner possible. We specialize in molecular, microbiology, and toxicology assays and technology. ASL is also a CDC ARLab Partner that works with the CDC to develop diagnostic tools to better identify emerging antibiotic resistance. For more information, visit .

Media Contacts

Nicole Ridgedale

Director of Corporate Marketing, LexaGene

800.215.1824 ext 206

Investor Relations

Jay Adelaar

Vice President of Capital Markets, LexaGene

800.215.1824 ext 207

The TSX Venture Exchange Inc. has in no way passed upon the merits of the proposed transaction and has neither approved nor disapproved the contents of this press release. Neither TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release.

This news release contains forward-looking information, which involves known and unknown risks, uncertainties and other factors that may cause actual events to differ materially from current expectation. Important factors -- including the availability of funds, the results of financing efforts, the success of technology development efforts, the cost to procure critical parts, performance of the instrument, market acceptance of the technology, regulatory acceptance, and licensing issues -- that could cause actual results to differ materially from the Company's expectations as disclosed in the Company's documents filed from time to time on SEDAR (see ). Readers are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date of this press release. The company disclaims any intention or obligation, except to the extent required by law, to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise.

EN
08/08/2019

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