Orally delivered MK-4482 inhibits SARS-CoV-2 replication in the Syrian hamster model

Author:

Rosenke Kyle,Hansen Frederick,Schwarz Benjamin,Feldmann Friederike,Haddock Elaine,Rosenke Rebecca,Barbian Kent,Meade-White Kimberly,Okumura Atsushi,Leventhal Shanna,Hawman David W.,Ricotta EmilyORCID,Bosio Catharine M.,Martens Craig,Saturday Greg,Feldmann HeinzORCID,Jarvis Michael A.ORCID

Abstract

AbstractThe COVID-19 pandemic progresses unabated in many regions of the world. An effective antiviral against SARS-CoV-2 that could be administered orally for use following high-risk exposure would be of substantial benefit in controlling the COVID-19 pandemic. Herein, we show that MK-4482, an orally administered nucleoside analog, inhibits SARS-CoV-2 replication in the Syrian hamster model. The inhibitory effect of MK-4482 on SARS-CoV-2 replication is observed in animals when the drug is administered either beginning 12 h before or 12 h following infection in a high-risk exposure model. These data support the potential utility of MK-4482 to control SARS-CoV-2 infection in humans following high-risk exposure as well as for treatment of COVID-19 patients.

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

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