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FDA Emergency Use Authorization Awarded to the Beckman Coulter Access IL-6 Test

The Access Interleukin-6 (IL-6) assay is designed to assist physicians in the identification of severe inflammatory response in COVID-19 patients

Written byBeckman Coulter Diagnostics andBeckman Coulter
| 3 min read
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BREA, CA — October 1, 2020 — Beckman Coulter today (Oct. 1) announced that it has received Emergency Use Authorization (EUA) for its Access Interleukin-6 (IL-6) assay from the US Food & Drug Administration (FDA). Access IL-6 is a fully automated immunoassay designed to detect IL-6 levels in serum and plasma which can be used to aid physicians identifying a severe inflammatory response and determining the risk of intubation with mechanical ventilation in COVID-19 patients.

IL-6 is a multifunctional cytokine that may promote inflammation in certain clinical conditions. Preliminary studies1 have shown that the IL-6 level is elevated in patients with severe COVID-19 and IL-6 may contribute to the severe inflammatory response, also sometimes referred to as cytokine storm.

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