Terumo BCT and Marker Therapeutics received FDA Emergency Use Authorization to treat acute respiratory failure in COVID-19 patients

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On Apr. 10, 2020, Terumo BCT and Marker Therapeutics announced the FDA issued an Emergency Use Authorization (EUA) for the use of Terumo BCTメs Spectra Optiaᆴ Apheresis System combined with Marker Therapeuticsメ D2000 Adsorption Cartridge to treat patients 18 years of age or older with confirmed Coronavirus Disease 2019 (COVID-19) admitted to the intensive care unit with confirmed or imminent respiratory failure to reduce pro-inflammatory cytokine levels.

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Source: erumo BCT, Inc.
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