Austin, TX (GLOBE NEWSWIRE) - Escher Biomedical Diagnostics, LLC announced that its Escher BT-MED® COV19 Saliva Test has been accepted by FDA as a Notification under Section IV.C of the Emergency Use Authorization program. The BT-MED® COV19 Test system is a high-throughput molecular method for detecting infection by the SARS-CoV-2 virus in specimens of saliva from individuals suspected of COVID-19 by their healthcare provider.
Through this Notification, Escher indicates its intent to distribute the COVID-19 virus test in the US while FDA review of the EUA request is pending. At present, the BT-MED® COV19 Test is for use only in CLIA-high-complexity laboratories.
"We are pleased to introduce this important method to the detection and characterization of pathogens. The novel approach developed by Biotrack BV allows fast and accurate detection of the COVID-19 virus within infected human cells that appear in saliva," stated Phil Speros of Escher. "And there are many advantages to saliva as a specimen, such as simplicity of collection, but also the ability to verify correct sample collection simply by observing the presence of the necessary small volume. These are important advantages over swab-based methods."
The BT-MED® diagnostic device is based on in situ hybridization with fluorescent molecular probe, coupled with automated intelligent digital image processing that evaluates as to the presence or absence of the virus. "There is no 'RT' and No 'PCR' because the BT-MED® COV19 method uses alternate methods to amplify the signal due to the virus."
Gerard Schouten, CEO of Biotrack BV, the manufacturer of the test system, comments, "After years of development our technology has come of age as a robust device that is simple to deploy and implement, even to challenging settings such as trucks and ships. Implementation in a clinical laboratory is easy." Schouten continued, "The fact that our system directly observes the molecular probe-lit viral nucleic acids in the infected human cells [shed in saliva] made it possible to create automated software to determine whether there is an infection or not."
About the BT-MED® System:
The BT-MED® system is composed of the BT-MED® Analyzer and test kits associated with specific pathogens or panels of pathogens. The Analyzer can be configured for full automated use, which minimizes the need for human technical activities, or partial automated use, which allows higher throughput.
The BT-MED® Analyzer and BT-MED® COV19 Test Kit is also CE Marked.
About Saliva as a Testing Specimen for COVID-19:
Saliva is a specimen type of interest, but other molecular approaches have seen variable results not always consistent with a very high accuracy testing. Increasing understanding of the biology of COVID-19 infections offers clear evidence that saliva contains cells that are quite useful in detecting the viral infection. (For example: https://www.nature.com/articles/s41591-021-01296-8 ). The BT-MED® method has distinct advantages in using saliva as a specimen type.
About Escher Biomedical Diagnostics, LLC:
Escher Biomedical Diagnostics, LLC is a joint venture between Biotrack BV, the Netherlands company that manufactures the BT-MED® Analyzer and COV19 Test Kit, and Echo Testing Group, LLC, an Austin, Texas company founded to bring the BT-MED® to the US and Canada, and Escher holds the exclusive marketing rights to do so.
About Biotrack BV
Biotrack BV, of Leeuwarden, Netherlands is the developer and manufacturer of the Biotrack-MED® system, branded in the US and Canada as BT-MED®. Besides medical applications, the platform technology has seen application in industrial and municipal monitoring applications. Biotrack BV is ISO13485 certified.
Legal Notice Regarding Forward-Looking Statements: This news release contains "Forward-looking Statements". These statements relate to future events or our future financial performance. These statements are only predictions and may differ materially from actual future results or events. We disclaim any intention or obligation to revise any forward-looking statements whether as a result of new information, future developments or otherwise. There are important risk factors that could cause actual results to differ from those contained in forward-looking statements, including, but not limited to our ability to fully commercialize our technology, risks associated with changes in general economic and business conditions, actions of our competitors, the extent to which we are able to develop new products and markets, the time and expense involved in such development activities, the ability to secure additional financing, the ability to consummate acquisitions and ultimately integrate them, the level of demand and market acceptance of our products, and changes in our business strategies. This is not an offering of securities and securities may not be offered or sold absent registration or an applicable exemption from the registration requirements.
© 2021 GlobeNewswire, Inc. All Rights Reserved.