Press Releases
Inflammatix Receives FDA Clearance for First-in-Class TriVerity™ Test
First and only molecular blood test that can both identify bacterial and viral infections and assess need for critical care
SUNNYVALE, Calif., January 21, 2025 /PRNewswire/ — Inflammatix, a pioneering host response diagnostics company, today announced that the U.S. Food and Drug Administration (FDA) has granted marketing authorization for the TriVerity™ Test System (TriVerity), a first-in-class molecular test for patients with suspected acute infection or sepsis. Using precise measurements of a patient’s immune response, TriVerity combines highly accurate bacterial-viral infection scoring with an all-cause illness severity risk evaluation, giving clinicians a rapid and holistic snapshot of a patient’s status.
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