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A review of the safety of favipiravir – a potential treatment in the COVID-19 pandemic?

机译:回顾法维吡韦的安全性-COVID-19大流行的潜在治疗方法?

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摘要

An observational study carried out in Shenzhen in February 2020 showed a significantly faster mean time to viral clearance of favipiravir than lopinavir/ritonavir [4 days 11 days ( <0.001)] . These results were supported by an early Chinese randomised clinical trial (RCT), where favipiravir treatment led to a significantly greater recovery rate in non-critical COVID-19 patients than umefenovir (71.4% 55.9% [ <0.05]) . Although neither were effective in boosting recovery rate for critically ill patients in this same trial [5.6% 0.0% (  = n.s.)] , these early results have led to further trials being instigated in China and Italy.
机译:2020年2月在深圳进行的一项观察性研究显示,与拉维那韦/利托那韦相比,法维拉韦的平均病毒清除平均时间明显更快[4天11天(<0.001)]。这些结果得到了一项早期的中国随机临床试验(RCT)的支持,在该试验中,非维拉韦治疗导致非关键COVID-19患者的恢复率显着高于梅芬诺韦(71.4%55.9%[<0.05])。尽管在同一项试验中[5.6%0.0%(n.s.)]都没有有效地提高危重患者的康复率,但这些早期结果导致在中国和意大利发起了进一步的试验。

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