Performance Evaluation of the LumiraDX SARS-CoV-2 Ag Ultra and LumiraDX SARS-CoV-2 & Flu A/B Tests at Point of Care (POC) Sites

CompletedOBSERVATIONAL
Enrollment

716

Participants

Timeline

Start Date

February 9, 2023

Primary Completion Date

April 11, 2023

Study Completion Date

April 11, 2023

Conditions
SARS-CoV-2Influenza AInfluenza BCOVID-19
Interventions
DIAGNOSTIC_TEST

LumiraDx SARS-CoV-2 Ag Ultra

The LumiraDx SARS-CoV-2 Ag Ultra Test is an automated rapid microfluidic immunofluorescence assay for use with the LumiraDx Platform intended for the qualitative detection of the nucleocapsid protein antigen to SARS-CoV-2 directly from anterior nasal swab samples collected from symptomatic individuals within the first twelve days of symptom onset suspected of COVID-19 by their healthcare provider.

DIAGNOSTIC_TEST

LumiraDx SARS-CoV-2 & Flu A/B

The LumiraDx SARS-CoV-2 \& Flu A/B test is an automated rapid microfluidic immunofluorescence assay for use with the LumiraDx Platform, for near-patient testing, intended for the qualitative detection and differentiation of SARS-CoV-2, Influenza A and/or Influenza B viral antigens from nasal swab samples.

Trial Locations (10)

23666

Meridian Clinical Research, LLC. / Velocity Clinical Research, Hampton

32720

Hillcrest Medical Research, LLC, DeLand

Hillcrest Medical Research, DeLand

33155

Marisela Gonzalez MD PA, Miami

68128

Barrett Clinic, La Vista

68510

Meridian Clinical Research, Lincoln

75211

Mercy Family Clinic, Dallas

84041

Alliance for Multispecialty Research, LLC, Layton

90717

Torrance Clinical Research Institute Inc., Lomita

92840

Paragon Rx Clinical, Inc, Garden Grove

All Listed Sponsors
lead

LumiraDx UK Limited

INDUSTRY