FDA to Allow for Plasma Therapy for COVID-19 Patients

Under emergency protocols, doctors can request to use survivors’ plasma to treat some critically ill COVID-19 patients.

Written byLisa Winter
| 3 min read

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Among the myriad clinical trials for vaccines to prevent COVID-19 and drugs to treat infections, doctors are looking to survivors’ plasma for a possible therapy. The US Food and Drug Administration (FDA) released a statement on Tuesday (March 24) stating that investigators can request to use plasma from COVID-19 survivors to deliver antibodies to seriously ill patients, under an emergency investigational new drug (IND) protocol.

Convalescent plasma treatment, as it is known, has roots stretching back over 100 years. It is based on the premise that because a survivor developed antibodies throughout the course of their own infection, blood donations to those who became recently ill would give the recipients’ immune systems a leg up, reducing the severity of the disease and increasing the likelihood of survival. During the 1918 Spanish flu pandemic, the rate of mortality decreased by as much as 50 percent among the ...

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Meet the Author

  • Lisa joined The Scientist in 2017. As social media editor, some of her duties include creating content, managing interactions, and developing strategies for the brand’s social media presence. She also contributes to the News & Opinion section of the website. Lisa holds a degree in Biological Sciences with a concentration in genetics, cell, and developmental biology from Arizona State University and has worked in science communication since 2012.

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