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Clinical Trial Summary

The specimens collected will be used to evaluate matrix equivalency in an immunoassay in development for the detection of IgG or IgA or IgM antibodies to SARS - CoV2 in human serum. These reagents are for in vitro diagnostic use only.


Clinical Trial Description

The objective of this study is to acquire paired serum, plasma and whole blood collected on a collection card from subjects with no known history of COVID-19 infection. The specimens will be collected at Biomerica in Irvine CA for specimen collection, banking, and matrix equivalency studies for projects in development at Biomerica for detection to IgG or IgA or IgM antibodies to Sars-CoV2 antibodies. Subject will also be asked to self-collect a nasal swab for COVID-19 PCR ;


Study Design


Related Conditions & MeSH terms

  • Focus in on Collecting Paired Specimens for Matrix Equivalency

NCT number NCT04468386
Study type Observational
Source Biomerica
Contact
Status Completed
Phase
Start date July 7, 2020
Completion date May 30, 2021