2021
DOI: 10.1007/s40267-021-00879-2
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What will be the role of molnupiravir in the treatment of COVID-19 infection?

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Cited by 18 publications
(13 citation statements)
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“… [2] Molnupiravir, being oral and also effective against newer COVID-19 variants, [8] is more practical and convenient for administration in ambulatory patients fulfilling the unmet need for safe and effective oral drugs in this population. [9] The huge reduction in the risk of mortality observed in our meta-analysis is highly encouraging. Future trials should evaluate the efficacy of molnupiravir in breakthrough infections as well as in comparison with other approved treatments for COVID-19.…”
mentioning
confidence: 55%
“… [2] Molnupiravir, being oral and also effective against newer COVID-19 variants, [8] is more practical and convenient for administration in ambulatory patients fulfilling the unmet need for safe and effective oral drugs in this population. [9] The huge reduction in the risk of mortality observed in our meta-analysis is highly encouraging. Future trials should evaluate the efficacy of molnupiravir in breakthrough infections as well as in comparison with other approved treatments for COVID-19.…”
mentioning
confidence: 55%
“…Recently, in the UK the oral antiviral agent molnupiravir has been approved, a potent ribonucleoside analogue that inhibits the replication of SARS-CoV-2, acting on the enzyme that the virus uses to generate copies of itself by introducing errors into its genetic code. Furthermore, the data indicate that molnupiravir reduced the risk of hospitalization or death in approximately 50% of adults who were at risk of a severe disease outcome [65]. The molnupiravir was authorized for distribution in emergency conditions by a Decree of the Ministry of Health on 26 November 2021 and is indicated within 5 days of the onset of symptoms.…”
Section: Management Of Patients With Post-covid Syndrome and After Ef...mentioning
confidence: 99%
“…The EIDD-triphosphate form inhibits RNA replication of virus. Molnupiravir reduces the ability of SARS-CoV-2 to replicate in the body, producing alterations (mutations) of the genetic material (RNA) of the virus during replication, so as to make it unable to multiply an adverse event in the molnupiravir group compared with the placebo group (1.3% vs 3.4%) (Vitiello et al 2021). Results from a clinical trial showed that 35.4% and 43.8% of individuals reported adverse events after administration of molnupiravir and placebo, respectively.…”
Section: Molnupiravirmentioning
confidence: 99%