Prospective Clinical Evaluation of the BioFire Emerging Coronavirus Panel for the Detection of COVID-19 and Other Coronaviruses

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorBioFire Defense LLC

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

1,500 Participants
are divided into 1 treatment group

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