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Clinical Trial Summary

This is an open label randomized controlled clinical trial which was designed to confirm the potential efficacy and safety of favipiravir in the management of patients with mild to moderate COVID-19 compared to best supportive care.


Clinical Trial Description

Favipiravir is an antiviral agent whose indication in Japan is currently for influenza infections. There were earlier reports from China suggesting its promising potential for benefit in the treatment of COVID-19. This is an open label randomized controlled clinical trial was designed to verify the potential efficacy and safety of favipiravir in the management of patients with mild to moderate COVID-19 compared to best supportive care. This study will look at the potential of using this repurposed oral agent in managing non-severe cases of COVID19. Consenting patients admitted to hospitals or isolation/quarantine facilities will be randomized at a 2:1 ratio to either favipiravir versus best supportive care. Patients will be examined daily and will have xray and nasopharyngeal swabs every 3-4 days for close monitoring. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05014373
Study type Interventional
Source University of the Philippines
Contact Regina Berba, MD
Phone +639985381599
Email rpberba@gmail.com
Status Recruiting
Phase Phase 3
Start date October 12, 2020
Completion date August 31, 2021

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