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Remdesivir in COVID-19: A critical review of pharmacology, pre-clinical and clinical studies

BACKGROUND & AIMS: Remdesivir is a broad spectrum anti-viral drug that has shown to inhibit SARS-CoV-2, in vitro and in vivo. In absence of any effective treatment for SARS-CoV-2 infection (COVID-19), remdesivir has been tried for a compassionate use in severe COVID-19. Newer randomized controll...

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Autores principales: Singh, Awadhesh Kumar, Singh, Akriti, Singh, Ritu, Misra, Anoop
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Diabetes India. Published by Elsevier Ltd. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214279/
https://www.ncbi.nlm.nih.gov/pubmed/32428865
http://dx.doi.org/10.1016/j.dsx.2020.05.018
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author Singh, Awadhesh Kumar
Singh, Akriti
Singh, Ritu
Misra, Anoop
author_facet Singh, Awadhesh Kumar
Singh, Akriti
Singh, Ritu
Misra, Anoop
author_sort Singh, Awadhesh Kumar
collection PubMed
description BACKGROUND & AIMS: Remdesivir is a broad spectrum anti-viral drug that has shown to inhibit SARS-CoV-2, in vitro and in vivo. In absence of any effective treatment for SARS-CoV-2 infection (COVID-19), remdesivir has been tried for a compassionate use in severe COVID-19. Newer randomized controlled studies that have recently become available, showed a mixed result. We aimed to systematically search the literature to understand the pharmacology and clinical effects of remdesivir in patients with COVID-19. METHODS: We systematically searched the PubMed, ClinicalTrial.Org and MedRxiv database up till May 5, 2020 using specific key words such as “Remdesivir” or ‘GS-5734″ AND “COVID-19” or “SARS-CoV-2” and retrieved all the article published in English language, that have reported the pharmacology and the clinical outcomes of remdesivir in patients with COVID-19. RESULTS: Initial compassionate use of remdesivir has shown a fairly good result, but difficult to quantify, in the absence of control arm. While the very first double-blind, placebo-controlled, randomized trial conducted in Wuhan, did not find any significant benefit compared to the control, the preliminary result of another similar multi-country trial has shown a significant faster time to recovery but without any difference in mortality. CONCLUSIONS: Remdesivir has shown a mixed result in patients with COVID-19 with an acceptable side effect. However, jury is still out while awaiting the results from the forthcoming trials.
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spelling pubmed-72142792020-05-12 Remdesivir in COVID-19: A critical review of pharmacology, pre-clinical and clinical studies Singh, Awadhesh Kumar Singh, Akriti Singh, Ritu Misra, Anoop Diabetes Metab Syndr Article BACKGROUND & AIMS: Remdesivir is a broad spectrum anti-viral drug that has shown to inhibit SARS-CoV-2, in vitro and in vivo. In absence of any effective treatment for SARS-CoV-2 infection (COVID-19), remdesivir has been tried for a compassionate use in severe COVID-19. Newer randomized controlled studies that have recently become available, showed a mixed result. We aimed to systematically search the literature to understand the pharmacology and clinical effects of remdesivir in patients with COVID-19. METHODS: We systematically searched the PubMed, ClinicalTrial.Org and MedRxiv database up till May 5, 2020 using specific key words such as “Remdesivir” or ‘GS-5734″ AND “COVID-19” or “SARS-CoV-2” and retrieved all the article published in English language, that have reported the pharmacology and the clinical outcomes of remdesivir in patients with COVID-19. RESULTS: Initial compassionate use of remdesivir has shown a fairly good result, but difficult to quantify, in the absence of control arm. While the very first double-blind, placebo-controlled, randomized trial conducted in Wuhan, did not find any significant benefit compared to the control, the preliminary result of another similar multi-country trial has shown a significant faster time to recovery but without any difference in mortality. CONCLUSIONS: Remdesivir has shown a mixed result in patients with COVID-19 with an acceptable side effect. However, jury is still out while awaiting the results from the forthcoming trials. Diabetes India. Published by Elsevier Ltd. 2020 2020-05-12 /pmc/articles/PMC7214279/ /pubmed/32428865 http://dx.doi.org/10.1016/j.dsx.2020.05.018 Text en © 2020 Diabetes India. Published by Elsevier Ltd. All rights reserved. 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 Article
Singh, Awadhesh Kumar
Singh, Akriti
Singh, Ritu
Misra, Anoop
Remdesivir in COVID-19: A critical review of pharmacology, pre-clinical and clinical studies
title Remdesivir in COVID-19: A critical review of pharmacology, pre-clinical and clinical studies
title_full Remdesivir in COVID-19: A critical review of pharmacology, pre-clinical and clinical studies
title_fullStr Remdesivir in COVID-19: A critical review of pharmacology, pre-clinical and clinical studies
title_full_unstemmed Remdesivir in COVID-19: A critical review of pharmacology, pre-clinical and clinical studies
title_short Remdesivir in COVID-19: A critical review of pharmacology, pre-clinical and clinical studies
title_sort remdesivir in covid-19: a critical review of pharmacology, pre-clinical and clinical studies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7214279/
https://www.ncbi.nlm.nih.gov/pubmed/32428865
http://dx.doi.org/10.1016/j.dsx.2020.05.018
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