FebriDx® Method Comparison Study Protocol

CompletedOBSERVATIONAL
Enrollment

800

Participants

Timeline

Start Date

December 20, 2024

Primary Completion Date

August 15, 2025

Study Completion Date

August 31, 2025

Conditions
Acute Respiratory Infections (ARIs)
Interventions
DIAGNOSTIC_TEST

Rapid point of care test to detect host immune response in ARI

FebriDx is a rapid lateral flow immunoassay for the visual, qualitative, in vitro detection of elevated levels of host response proteins, Myxovirus resistance protein A (MxA) and C-reactive protein (CRP), directly from fingerstick blood to aid in the differentiation of bacterial from non-bacterial acute respiratory infections.

Trial Locations (8)

32763

Hillcrest Medical Research, LLC, Orange City

33027

Trujillo Medical Center, Miramar

33144

L&C, Miami

45430

Hometown Urgent Care and Research, Beavercreek

76021

HMG Clinical Research/Herrera Medical Group, Bedford

77494

Ascada Health, Katy

91105

Exer Urgent Care, Pasadena

92835

Ascada Health, Fullerton

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Biomedical Advanced Research and Development Authority

FED

lead

Lumos Diagnostics

INDUSTRY

NCT06746259 - FebriDx® Method Comparison Study Protocol | Biotech Hunter | Biotech Hunter