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Current pharmacological treatments for SARS-COV-2: A narrative review

The novel coronavirus, later identified as SARS-CoV-2, originating from Wuhan in China in November 2019, quickly spread around the world becoming a pandemic. Despite the knowledge of previous coronaviruses, such as those responsible for the SARS and MERS-CoV epidemic, there is no drug or prophylaxis...

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Autores principales: Nittari, Giulio, Pallotta, Graziano, Amenta, Francesco, Tayebati, Seyed Khosrow
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7320862/
https://www.ncbi.nlm.nih.gov/pubmed/32603692
http://dx.doi.org/10.1016/j.ejphar.2020.173328
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author Nittari, Giulio
Pallotta, Graziano
Amenta, Francesco
Tayebati, Seyed Khosrow
author_facet Nittari, Giulio
Pallotta, Graziano
Amenta, Francesco
Tayebati, Seyed Khosrow
author_sort Nittari, Giulio
collection PubMed
description The novel coronavirus, later identified as SARS-CoV-2, originating from Wuhan in China in November 2019, quickly spread around the world becoming a pandemic. Despite the knowledge of previous coronaviruses, such as those responsible for the SARS and MERS-CoV epidemic, there is no drug or prophylaxis treatment to this day. The rapid succession of scientific findings on SARS-CoV-2 provides a significant number of potential drug targets. Nevertheless, at the same time, the high quantity of clinical data, generated by a large number of rapidly infected people, require accurate tests regarding effective medical treatments. Several in vitro and in vivo studies were rapidly initiated after the outbreak of the pandemic COVID-19. Initial clinical studies revealed the promising potential of remdesivir that demonstrated a powerful and specific in vitro antiviral activity for COVID-19. Promising effects appear to be attributable to hydroxychloroquine. Remdesivir and hydroxychloroquine are being tested in ongoing randomized trials. In contrast, oseltamivir was not effective and corticosteroids are not currently recommended. However, few data from ongoing clinical trials are identifying low molecular weight heparins, innate immune system stimulating agents, and inflammatory modulating agents as potential effective agents. The authors assume that the current pandemic will determine the need for a systematic approach based on big data analysis for identifying effective drugs to defeat SARS-Cov-2. This work is aimed to be a general reference point and to provide an overview as comprehensive as possible regarding the main clinical trials in progress at the moment.
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spelling pubmed-73208622020-06-29 Current pharmacological treatments for SARS-COV-2: A narrative review Nittari, Giulio Pallotta, Graziano Amenta, Francesco Tayebati, Seyed Khosrow Eur J Pharmacol Article The novel coronavirus, later identified as SARS-CoV-2, originating from Wuhan in China in November 2019, quickly spread around the world becoming a pandemic. Despite the knowledge of previous coronaviruses, such as those responsible for the SARS and MERS-CoV epidemic, there is no drug or prophylaxis treatment to this day. The rapid succession of scientific findings on SARS-CoV-2 provides a significant number of potential drug targets. Nevertheless, at the same time, the high quantity of clinical data, generated by a large number of rapidly infected people, require accurate tests regarding effective medical treatments. Several in vitro and in vivo studies were rapidly initiated after the outbreak of the pandemic COVID-19. Initial clinical studies revealed the promising potential of remdesivir that demonstrated a powerful and specific in vitro antiviral activity for COVID-19. Promising effects appear to be attributable to hydroxychloroquine. Remdesivir and hydroxychloroquine are being tested in ongoing randomized trials. In contrast, oseltamivir was not effective and corticosteroids are not currently recommended. However, few data from ongoing clinical trials are identifying low molecular weight heparins, innate immune system stimulating agents, and inflammatory modulating agents as potential effective agents. The authors assume that the current pandemic will determine the need for a systematic approach based on big data analysis for identifying effective drugs to defeat SARS-Cov-2. This work is aimed to be a general reference point and to provide an overview as comprehensive as possible regarding the main clinical trials in progress at the moment. Elsevier B.V. 2020-09-05 2020-06-27 /pmc/articles/PMC7320862/ /pubmed/32603692 http://dx.doi.org/10.1016/j.ejphar.2020.173328 Text en © 2020 Elsevier B.V. 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
Nittari, Giulio
Pallotta, Graziano
Amenta, Francesco
Tayebati, Seyed Khosrow
Current pharmacological treatments for SARS-COV-2: A narrative review
title Current pharmacological treatments for SARS-COV-2: A narrative review
title_full Current pharmacological treatments for SARS-COV-2: A narrative review
title_fullStr Current pharmacological treatments for SARS-COV-2: A narrative review
title_full_unstemmed Current pharmacological treatments for SARS-COV-2: A narrative review
title_short Current pharmacological treatments for SARS-COV-2: A narrative review
title_sort current pharmacological treatments for sars-cov-2: a narrative review
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7320862/
https://www.ncbi.nlm.nih.gov/pubmed/32603692
http://dx.doi.org/10.1016/j.ejphar.2020.173328
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