Abstract
In May 2020 the Russian Ministry of Health granted fast-Track marketing authorization to RNA polymerase inhibitor AVIFAVIR (favipiravir) for the treatment of COVID-19 patients. In the pilot stage of Phase II/III clinical trial, AVIFAVIR enabled SARS-CoV-2 viral clearance in 62.5% of patients within 4 days, and was safe and well-Tolerated. Clinical Trials Registration. NCT04434248.
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Ivashchenko, A. A., Dmitriev, K. A., Vostokova, N. V., Azarova, V. N., Blinow, A. A., Egorova, A. N., … Ivachtchenko, A. V. (2021). AVIFAVIR for Treatment of Patients with Moderate Coronavirus Disease 2019 (COVID-19): Interim Results of a Phase II/III Multicenter Randomized Clinical Trial. Clinical Infectious Diseases, 73(3), 531–534. https://doi.org/10.1093/cid/ciaa1176
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