POC Performance Evaluation of LumiraDx SARS-CoV-2 Ag Ultra and SARS-CoV-2 & Flu A/B Tests.

Completed

Conditions studied: SARS-CoV-2, Influenza A, Influenza B, COVID-19

In brief

This is a prospective multicenter study conducted to evaluate the performance of the LumiraDx SARS-CoV-2 Ag Ultra test in detecting severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and LumiraDx SARS-CoV-2 \& Flu A/B test in differential detection of SARS-CoV-2, Influenza A (Flu A) and Influenza B (Flu B) at point of care sites. Subjects presenting with symptoms suggestive of coronavirus disease 2019 (COVID-19) and/or Influenza at the time of the study visit will be enrolled and asked to donate swab sample(s) for testing in the device(s) under evaluation.

Key facts

Study ID

NCT05728970

Run by

LumiraDx UK Limited

People needed

716

Starts

2023-02-09

Expected to finish

2023-04-11

Last updated by the study team

2026-06-12

Who can join

Age: any. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Subject may be of any age or sex.
• Self-reported symptoms by the subject and/or preliminary assessment of the subject by the Investigator/designee should be suggestive of COVID-19 and/or Influenza at the time of the study visit. The subject must present as symptomatic, exhibiting one or more of the following signs and symptoms: fever, cough, shortness of breath, difficulty breathing, muscle pain, headache, sore throat, chills, repeated shaking with chills, new loss of taste or smell congestion or runny nose, diarrhea, nausea or vomiting. The onset of these symptoms will be recorded and will be within the last twelve (12) days.
• Participant (or parent/legal guardian) capable and willing to give informed consent/assent.

You may not qualify if…

• The subject underwent a nasal wash/aspirate as part of standard of care testing during this study visit.
• The subject is currently receiving or has received within the past thirty (30) days of the study visit an experimental biologic, drug, or device including either treatment or therapy.
• Subjects undergoing treatment currently and/or within the past thirty (30) days of the study with medication to treat novel Coronavirus SARS-CoV-2 viral infections, which may include but is not limited to; COVID-19 antivirals (Lagevrio, PAXLOVID), Remdesivir (Veklury) or receiving convalescent plasma therapy for SARS-CoV-2.
• Subjects undergoing treatment currently and/or within the past fourteen (14) days of the study visit with an inhaled influenza vaccine (FluMist®) or with anti-viral medication, which may include but is not limited to Amantadine (Symmetrel®), Rimantadine (Flumadine®), Zanamivir (Relenza®), Oseltamivir (Tamiflu®), Baloxavir Marboxil (Xofluza™), Palivizumab (Synagis®), or ribavirin.
• The subject previously participated in this study.

Where it is running

• Paragon Rx Clinical, Inc — Garden Grove, California, United States
• Torrance Clinical Research Institute Inc. — Lomita, California, United States
• Hillcrest Medical Research, LLC — DeLand, Florida, United States
• Hillcrest Medical Research — DeLand, Florida, United States
• Marisela Gonzalez MD PA — Miami, Florida, United States
• Barrett Clinic — La Vista, Nebraska, United States
• Meridian Clinical Research — Lincoln, Nebraska, United States
• Mercy Family Clinic — Dallas, Texas, United States
• Alliance for Multispecialty Research, LLC — Layton, Utah, United States
• Meridian Clinical Research, LLC. / Velocity Clinical Research — Hampton, Virginia, United States

Full record on ClinicalTrials.gov

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