Remdesivir for severe acute respiratory syndrome coronavirus 2 causing COVID-19: An evaluation of the evidence
Identifieur interne : 001895 ( Pmc/Curation ); précédent : 001894; suivant : 001896Remdesivir for severe acute respiratory syndrome coronavirus 2 causing COVID-19: An evaluation of the evidence
Auteurs : Yu-Chen Cao [République populaire de Chine] ; Qi-Xin Deng [République populaire de Chine] ; Shi-Xue Dai [République populaire de Chine]Source :
- Travel Medicine and Infectious Disease [ 1477-8939 ] ; 2020.
Abstract
The novel coronavirus infection that initially found at the end of 2019 has attracted great attention. So far, the number of infectious cases has increased globally to more than 100 thousand and the outbreak has been defined as a pandemic situation, but there are still no “specific drug” available. Relevant reports have pointed out the novel coronavirus has 80% homology with SARS. In the difficulty where new synthesized drug cannot be applied immediately to patients, “conventional drug in new use” becomes a feasible solution. The first medication experience of the recovered patients in the US has led remdesivir to be the “specific drug”. China has also taken immediate action to put remdesivir into clinical trials with the purpose of applying it into clinical therapeutics for Corona Virus Disease 2019 (COVID-19). We started from the structure, immunogenicity, and pathogenesis of coronavirus infections of the novel coronavirus. Further, we analyzed the pharmacological actions and previous trials of remdesivir to identify the feasibility of conducting experiments on COVID-19.
Url:
DOI: 10.1016/j.tmaid.2020.101647
PubMed: 32247927
PubMed Central: 7151266
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<front><div type="abstract" xml:lang="en"><p>The novel coronavirus infection that initially found at the end of 2019 has attracted great attention. So far, the number of infectious cases has increased globally to more than 100 thousand and the outbreak has been defined as a pandemic situation, but there are still no “specific drug” available. Relevant reports have pointed out the novel coronavirus has 80% homology with SARS. In the difficulty where new synthesized drug cannot be applied immediately to patients, “conventional drug in new use” becomes a feasible solution. The first medication experience of the recovered patients in the US has led remdesivir to be the “specific drug”. China has also taken immediate action to put remdesivir into clinical trials with the purpose of applying it into clinical therapeutics for Corona Virus Disease 2019 (COVID-19). We started from the structure, immunogenicity, and pathogenesis of coronavirus infections of the novel coronavirus. Further, we analyzed the pharmacological actions and previous trials of remdesivir to identify the feasibility of conducting experiments on COVID-19.</p>
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<pmc article-type="review-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Travel Med Infect Dis</journal-id>
<journal-id journal-id-type="iso-abbrev">Travel Med Infect Dis</journal-id>
<journal-title-group><journal-title>Travel Medicine and Infectious Disease</journal-title>
</journal-title-group>
<issn pub-type="ppub">1477-8939</issn>
<issn pub-type="epub">1873-0442</issn>
<publisher><publisher-name>Elsevier Ltd.</publisher-name>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">32247927</article-id>
<article-id pub-id-type="pmc">7151266</article-id>
<article-id pub-id-type="publisher-id">S1477-8939(20)30116-2</article-id>
<article-id pub-id-type="doi">10.1016/j.tmaid.2020.101647</article-id>
<article-id pub-id-type="publisher-id">101647</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Article</subject>
</subj-group>
</article-categories>
<title-group><article-title>Remdesivir for severe acute respiratory syndrome coronavirus 2 causing COVID-19: An evaluation of the evidence</article-title>
</title-group>
<contrib-group><contrib contrib-type="author" id="au1"><name><surname>Cao</surname>
<given-names>Yu-chen</given-names>
</name>
<xref rid="aff1" ref-type="aff">a</xref>
<xref rid="fn1" ref-type="fn">1</xref>
</contrib>
<contrib contrib-type="author" id="au2"><name><surname>Deng</surname>
<given-names>Qi-xin</given-names>
</name>
<xref rid="aff1" ref-type="aff">a</xref>
<xref rid="fn1" ref-type="fn">1</xref>
</contrib>
<contrib contrib-type="author" id="au3"><name><surname>Dai</surname>
<given-names>Shi-xue</given-names>
</name>
<email>shixuedai@hotmail.com</email>
<xref rid="aff2" ref-type="aff">b</xref>
<xref rid="cor1" ref-type="corresp">∗</xref>
</contrib>
</contrib-group>
<aff id="aff1"><label>a</label>
The Second Clinical School, Southern Medical University, Guangzhou, 510515, Guangdong, China</aff>
<aff id="aff2"><label>b</label>
Department of Gastroenterology, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, South China University of Technology, Guangzhou, 510080, Guangdong, China</aff>
<author-notes><corresp id="cor1"><label>∗</label>
Corresponding author. <email>shixuedai@hotmail.com</email>
</corresp>
<fn id="fn1"><label>1</label>
<p id="ntpara0010">The two authors are equal in contribution to this review.</p>
</fn>
</author-notes>
<pub-date pub-type="pmc-release"><day>2</day>
<month>4</month>
<year>2020</year>
</pub-date>
<pmc-comment> PMC Release delay is 0 months and 0 days and was based on .</pmc-comment>
<pub-date pub-type="epub"><day>2</day>
<month>4</month>
<year>2020</year>
</pub-date>
<elocation-id>101647</elocation-id>
<history><date date-type="received"><day>5</day>
<month>3</month>
<year>2020</year>
</date>
<date date-type="rev-recd"><day>17</day>
<month>3</month>
<year>2020</year>
</date>
<date date-type="accepted"><day>26</day>
<month>3</month>
<year>2020</year>
</date>
</history>
<permissions><copyright-statement>© 2020 Elsevier Ltd. All rights reserved.</copyright-statement>
<copyright-year>2020</copyright-year>
<copyright-holder>Elsevier Ltd</copyright-holder>
<license><license-p>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.</license-p>
</license>
</permissions>
<abstract id="abs0010"><p>The novel coronavirus infection that initially found at the end of 2019 has attracted great attention. So far, the number of infectious cases has increased globally to more than 100 thousand and the outbreak has been defined as a pandemic situation, but there are still no “specific drug” available. Relevant reports have pointed out the novel coronavirus has 80% homology with SARS. In the difficulty where new synthesized drug cannot be applied immediately to patients, “conventional drug in new use” becomes a feasible solution. The first medication experience of the recovered patients in the US has led remdesivir to be the “specific drug”. China has also taken immediate action to put remdesivir into clinical trials with the purpose of applying it into clinical therapeutics for Corona Virus Disease 2019 (COVID-19). We started from the structure, immunogenicity, and pathogenesis of coronavirus infections of the novel coronavirus. Further, we analyzed the pharmacological actions and previous trials of remdesivir to identify the feasibility of conducting experiments on COVID-19.</p>
</abstract>
<kwd-group id="kwrds0010"><title>Keywords</title>
<kwd>Severe acute respiratory syndrome coronavirus 2</kwd>
<kwd>Corona virus disease 2019</kwd>
<kwd>Remdesivir</kwd>
<kwd>Phase III clinical trial</kwd>
</kwd-group>
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