Orally administered epeleuton inhibits SARS-CoV-2 viral load, replication and pathology in the Syrian Hamster model

Climax, J.; Hamza, M.; Lafferty, A.; Guilfoyle, K.; van Amerongen, G.; Stadler, K.; Wohlsein, P.; Baumgärtner, W.; Weissbach, M.; Coughlan, D.

doi:10.1101/2021.12.07.471588

bioRxiv · 10.1101/2021.12.07.471588

Orally administered epeleuton inhibits SARS-CoV-2 viral load, replication and pathology in the Syrian Hamster model

Climax, J.·Hamza, M.·Lafferty, A.·Guilfoyle, K.·van Amerongen, G.·Stadler, K.·Wohlsein, P.·Baumgärtner, W.·Weissbach, M.·Coughlan, D.

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Abstract

Early treatment of patients with confirmed COVID-19 presenting mild symptoms can reduce the number that progress to more severe disease and require hospitalization. Considering the potential for the development of drug resistance to existing therapies and the emergence of new SARS-CoV-2 variants, there is a need for an expanded armamentarium of treatment options for COVID-19. Epeleuton is a novel orally administered second-generation n-3 fatty acid with potential direct antiviral and immunomodulatory actions, and a favourable clinical safety profile. In this study we show that epeleuton inhibits SARS-CoV-2 infectious viral load, replication and disease pathology in the lungs and upper airways in the Syrian hamster model of SARS-CoV-2 infection. These data support the potential utility of epeleuton in the early treatment and prevention of SARS-CoV-2 infection. Clinical trials are needed to evaluate the efficacy of epeleuton as an outpatient treatment and prevention of COVID-19.

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Climax, J., Hamza, M., Lafferty, A., Guilfoyle, K., van Amerongen, G., Stadler, K., Wohlsein, P., Baumgärtner, W., Weissbach, M., Coughlan, D.. 2021-12-09. Orally administered epeleuton inhibits SARS-CoV-2 viral load, replication and pathology in the Syrian Hamster model. https://doi.org/10.1101/2021.12.07.471588

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