GENOMADIX ANNOUNCES FDA CLEARANCE TO MARKET THE GENOMADIX CUBE CYP2C19 SYSTEM

OTTAWA, ON, March 22, 2023 /CNW/ - Genomadix, based in Ottawa, Canada, announced today the US Food and Drug Administration (FDA) granted 510(k) clearance permitting marketing of its "Genomadix Cube^TM CYP2C19 System" (Cube CYP2C19 test), an automated sample-to-result PCR test.

The Cube CYP2C19 test can be used to aid clinicians in determining therapeutic strategy for drugs metabolized by the CYP450 2C19 genetic pathway. Genomadix Cube CYP2C19 System identifies the CYP2C19 *2, *3, and *17 alleles, if present, directly from buccal swab in about an hour.

"The Genomadix Cube CYP2C19 System empowers physicians to make informed decisions on appropriate drug selection for a number of precision medicine indications such as antiplatelet therapy in both stroke and cardiology patients," said Steve Edgett, Genomadix's Chief Executive Officer. "This achievement represents a milestone for Genomadix. Genomadix is excited to commence precision medicine commercialization activities in the United States."

The Genomadix Cube is a polymerase chain reaction (PCR) molecular diagnostic instrument capable of performing tests for genetic, infectious disease, and environmental targets on a sample-to-result platform. The portable size, ease of use, and on-demand processing capability enables users to generate time-critical results.

The Genomadix Cube CYP2C19 System is commercially distributed in Europe, as well as all countries recognizing the CE Mark (CE-IVD).

The CYP2C19 enzyme plays a role in metabolizing at least 10% of current clinically used drugs including anti-platelet medication, antidepressants, and proton pump inhibitors.^1,2 Genetic variability of CYP2C19 can affect the clinical effectiveness and safety of these drugs.² Approximately 3 in 10 people carry high risk mutations that can impair the function of affected drugs.¹

Genomadix Inc. is a pioneer in real-time RT-PCR point of use technology, dedicated to the highest level of customer satisfaction, quality, and support, maintaining ISO 13485 medical device development and manufacturing standards certification. Based in Ottawa, Canada, the Genomadix Cube automates complex and tedious manual procedures, advancing sample to result DNA/RNA testing in clinical, environmental, infectious disease, and precision medicine. For more information, visit www.genomadix.com.

SOURCE Genomadix