About this trial
The Biomedical Advanced Research and Development Authority (BARDA) has contracted BioFire Defense (BFDf) to develop the BioFire Emerging Coronavirus (ECoV) Panel, a nucleic acid test capable of detecting coronaviruses from nasopharyngeal swab (NPS) in transport medium.
This study aims to evaluate the diagnostic accuracy of the assays comprising the BioFire ECoV Panel. It is hypothesized that the BioFire ECoV Panel assays will be highly sensitive and specific for the detection of the coronaviruses included on the panel.
Eligibility criteria
Qualifiers
Specimen is residual NPS in transport medium (VTM or UTM) left over from standard of care testing under clinician order for respiratory pathogen analysis.
Specimen has been held at room temperature for less than or equal to 4 hours or 4°C for less than or equal to 72 hours before enrollment.
At least 1.7 mL of specimen is remaining after standard of care testing and available for use in the study
Disqualifiers
Specimen is unable to be tested within the defined storage parameters
Insufficient specimen volume for testing
Transport medium type is unknown
Trial design
Treatments tested in this trial
- Investigational IVD for coronaviruses
Treatment groups
Sponsors and collaborators
BioFire Defense LLC
Lead sponsor
Children's Hospital Los Angeles
Collaborator
George Washington University
Collaborator
Wake Forest University Health Sciences
Collaborator
Tampa General Hospital
Collaborator
The University of Texas Medical Branch, Galveston
Collaborator
Emory University
Collaborator