Author: Ivashchenko, A. A.; Dmitriev, K. A.; Vostokova, N. V.; Azarova, V. N.; Blinow, A. A.; Egorova, A. N.; Gordeev, I. G.; Ilin, A. P.; Karapetian, R. N.; Kravchenko, D. V.; Lomakin, N. V.; Merkulova, E. A.; Papazova, N. A.; Pavlikova, E. P.; Savchuk, N. P.; Simakina, E. N.; Sitdekov, T. A.; Smolyarchuk, E. A.; Tikhomolova, E. G.; Yakubova, E. V.; Ivachtchenko, A. V.
Title: Interim Results of a Phase II/III Multicenter Randomized Clinical Trial of AVIFAVIR in Hospitalized Patients with COVID-19 Cord-id: sw48iegh Document date: 2020_8_4
ID: sw48iegh
Snippet: 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.
Document: 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.
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