Usability and Clinical Validation of the Flu A/B/COVID-19 + RSV Multiplex Rapid Test

Authors
Category Primary study
Registry of TrialsClinicalTrials.gov
Year 2026
This will be a prospective study for the clinical validation of the CorDx Tyfast Flu A/B/COVID-19 + RSV Multiplex Rapid Test for the qualitative detection and differentiation of SARS-CoV-2, Influenza A, Influenza B and RSV in AN samples. Results from the CorDx Tyfast Flu A/B/COVID-19 + RSV Multiplex Rapid Test will be compared to results from a 510(k) cleared highly sensitive, multi-analyte reverse transcriptase polymerase chain reaction (RT-PCR) test for SARS-CoV-2, Influenza A, Influenza B and RSV, such as the 510(k) cleared Cepheid Xpert Xpress CoV-2/Flu/RSV plus (K250995).
Epistemonikos ID: 16cbbb9543c0b821d0f7cbd6d55f9fee1b15f0a4
First added on: Oct 16, 2026