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Therapeutic dilemmas in addressing SARS-CoV-2 infection: Favipiravir versus Remdesivir

Coronavirus disease 2019 (COVID-19) represents an unmet clinical need, due to a high mortality rate, rapid mutation rate in the virus, increased chances of reinfection, lack of effectiveness of repurposed drugs and economic damage. COVID-19 pandemic has created an urgent need for effective molecules...

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Autores principales: Negru, Paul Andrei, Radu, Andrei-Flavius, Vesa, Cosmin Mihai, Behl, Tapan, Abdel-Daim, Mohamed M., Nechifor, Aurelia Cristina, Endres, Laura, Stoicescu, Manuela, Pasca, Bianca, Tit, Delia Mirela, Bungau, Simona Gabriela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Published by Elsevier Masson SAS. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8813547/
https://www.ncbi.nlm.nih.gov/pubmed/35131656
http://dx.doi.org/10.1016/j.biopha.2022.112700
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author Negru, Paul Andrei
Radu, Andrei-Flavius
Vesa, Cosmin Mihai
Behl, Tapan
Abdel-Daim, Mohamed M.
Nechifor, Aurelia Cristina
Endres, Laura
Stoicescu, Manuela
Pasca, Bianca
Tit, Delia Mirela
Bungau, Simona Gabriela
author_facet Negru, Paul Andrei
Radu, Andrei-Flavius
Vesa, Cosmin Mihai
Behl, Tapan
Abdel-Daim, Mohamed M.
Nechifor, Aurelia Cristina
Endres, Laura
Stoicescu, Manuela
Pasca, Bianca
Tit, Delia Mirela
Bungau, Simona Gabriela
author_sort Negru, Paul Andrei
collection PubMed
description Coronavirus disease 2019 (COVID-19) represents an unmet clinical need, due to a high mortality rate, rapid mutation rate in the virus, increased chances of reinfection, lack of effectiveness of repurposed drugs and economic damage. COVID-19 pandemic has created an urgent need for effective molecules. Clinically proven efficacy and safety profiles have made favipiravir (FVP) and remdesivir (RDV) promising therapeutic options for use against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. Even though both are prodrug molecules with an antiviral role based on a similar mechanism of action, differences in pharmacological, pharmacokinetic and pharmacotoxicological mechanisms have been identified. The present study aims to provide a comprehensive comparative assessment of FVP and RDV against SARS-CoV-2 infections, by centralizing medical data provided by significant literature and authorized clinical trials, focusing on the importance of a better understanding of the interactions between drug molecules and infectious agents in order to improve the global management of COVID-19 patients and to reduce the risk of antiviral resistance.
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spelling pubmed-88135472022-02-04 Therapeutic dilemmas in addressing SARS-CoV-2 infection: Favipiravir versus Remdesivir Negru, Paul Andrei Radu, Andrei-Flavius Vesa, Cosmin Mihai Behl, Tapan Abdel-Daim, Mohamed M. Nechifor, Aurelia Cristina Endres, Laura Stoicescu, Manuela Pasca, Bianca Tit, Delia Mirela Bungau, Simona Gabriela Biomed Pharmacother Review Coronavirus disease 2019 (COVID-19) represents an unmet clinical need, due to a high mortality rate, rapid mutation rate in the virus, increased chances of reinfection, lack of effectiveness of repurposed drugs and economic damage. COVID-19 pandemic has created an urgent need for effective molecules. Clinically proven efficacy and safety profiles have made favipiravir (FVP) and remdesivir (RDV) promising therapeutic options for use against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. Even though both are prodrug molecules with an antiviral role based on a similar mechanism of action, differences in pharmacological, pharmacokinetic and pharmacotoxicological mechanisms have been identified. The present study aims to provide a comprehensive comparative assessment of FVP and RDV against SARS-CoV-2 infections, by centralizing medical data provided by significant literature and authorized clinical trials, focusing on the importance of a better understanding of the interactions between drug molecules and infectious agents in order to improve the global management of COVID-19 patients and to reduce the risk of antiviral resistance. The Authors. Published by Elsevier Masson SAS. 2022-03 2022-02-04 /pmc/articles/PMC8813547/ /pubmed/35131656 http://dx.doi.org/10.1016/j.biopha.2022.112700 Text en © 2022 The Authors Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Review
Negru, Paul Andrei
Radu, Andrei-Flavius
Vesa, Cosmin Mihai
Behl, Tapan
Abdel-Daim, Mohamed M.
Nechifor, Aurelia Cristina
Endres, Laura
Stoicescu, Manuela
Pasca, Bianca
Tit, Delia Mirela
Bungau, Simona Gabriela
Therapeutic dilemmas in addressing SARS-CoV-2 infection: Favipiravir versus Remdesivir
title Therapeutic dilemmas in addressing SARS-CoV-2 infection: Favipiravir versus Remdesivir
title_full Therapeutic dilemmas in addressing SARS-CoV-2 infection: Favipiravir versus Remdesivir
title_fullStr Therapeutic dilemmas in addressing SARS-CoV-2 infection: Favipiravir versus Remdesivir
title_full_unstemmed Therapeutic dilemmas in addressing SARS-CoV-2 infection: Favipiravir versus Remdesivir
title_short Therapeutic dilemmas in addressing SARS-CoV-2 infection: Favipiravir versus Remdesivir
title_sort therapeutic dilemmas in addressing sars-cov-2 infection: favipiravir versus remdesivir
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8813547/
https://www.ncbi.nlm.nih.gov/pubmed/35131656
http://dx.doi.org/10.1016/j.biopha.2022.112700
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