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| Study characteristics | |
| Methods | Randomized placebo‐controlled trial |
| Participants | PCR‐confirmed COVID‐19 |
| Interventions | Favipiravir, placebo |
| Outcomes | The primary endpoint was time to virological cure, defined as 2 successive swabs negative for SARS‐CoV‐2 by PCR. Secondary outcomes were progression of disease severity, symptom resolution, and safety. |
| Notes | |
