Regulators Could Allow Early Use of COVID-19 Vaccine or Treatment

7 Pages Posted: 7 Apr 2020

See all articles by Ben Yeoh

Ben Yeoh

Hoffman Centre (Chatham House)

Date Written: March 24, 2020

Abstract

Quickly developed therapeutic, prophylactic, and vaccine treatments will be essential to defeat the COVID-19 pandemic. Standard regulatory and development protocols typically yield drug development in 6 to 11 years. However, experimental vaccines and prophylactics against COVID-19 are in development and currently in trials, making deployment after safety trials feasible within months. Though efficacy of these treatments is uncertain, with probability of success, on average, at just 16 percent, efficacy can still be tested in real-world settings by adopting an approach that allows patients to begin drug treatments earlier in the regulatory process.

Keywords: immunization, vaccines, healthcare, coronavirus, coronavirus pandemic, COVID-19, public health, economics, quarantine, economy, economic crisis

JEL Classification: I00, I18

Suggested Citation

Yeoh, Ben, Regulators Could Allow Early Use of COVID-19 Vaccine or Treatment (March 24, 2020). Special Edition Policy Brief, Available at SSRN: https://ssrn.com/abstract=3570041 or http://dx.doi.org/10.2139/ssrn.3570041

Ben Yeoh (Contact Author)

Hoffman Centre (Chatham House) ( email )

United States

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