Early randomized trials are unable to provide evidence for reducing time to clinical improvement, clearance of virus, or mortality amongst those given Remdesivir as COVID-19 intervention
Although initial observational studies suggested high hopes for drug efficacy, a randomized, double-blind, placebo-controlled clinical trial was unable to prove statistical significance for reducing the following among severe COVID-19 patients hospitalized in Wuhan, China:
- Clinical improvement
- Clearance of virus
- Mortality rates The investigators were forced to stop the study early after no additional patients met the eligibility criteria. The trial was deemed underpowered (58% power), therefore limiting study findings.
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Early randomized trials are unable to provide evidence for reducing time to clinical improvement, clearance of virus, or mortality amongst those given Remdesivir as COVID-19 intervention
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