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NCT04959760

BinaxNow COVID-19 IgG Rapid Test Device and Antibody Self Test

Completed NA Last updated 9 May 2022
What this trial tests

NA trial testing The BinaxNOW™ Antibody Tests measure IgG antibodies against SARS-CoV-2. in COVID-19 Respiratory Infection in 263 participants. Completed in 20 January 2022.

Timeline
3 June 2021
Primary endpoint
20 January 2022
20 January 2022

Quick facts

Lead sponsorAbbott Rapid Diagnostics Jena GmbH
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposediagnostic
Enrollment263
Start date3 June 2021
Primary completion20 January 2022
Estimated completion20 January 2022
Sites5 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Abbott Rapid Diagnostics Jena GmbH

Who can join

18 and older, any sex, with COVID-19 Respiratory Infection. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Performance evaluation of the BinaxNOW™ COVID-19 IgG Rapid Test Device (Professional Use) and with BinaxNOW™ COVID-19 Antibody Self Test wehn used with fingerstick capillary whole blood and plasma samples. The BinaxNOW™ Antibody Tests are lateral flow tests that measure SARS-CoV-2 IgG antibodies.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for COVID-19 Respiratory Infection

Currently open trials in the same condition.

Other Abbott Rapid Diagnostics Jena GmbH trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04959760.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing