No shortcuts to SARS-CoV-2 antivirals
Are many drug repurposers pursuing artifacts? When the COVID-19 pandemic hit, there was massive investment into the discovery of new treatments. Given the urgent need, repurposing of approved or clinically pretested drugs appeared especially attractive because that strategy promised fast initiation...
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Veröffentlicht in: | Science (American Association for the Advancement of Science) 2021-07, Vol.373 (6554), p.488-489 |
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creator | Edwards, Aled Hartung, Ingo V. |
description | Are many drug repurposers pursuing artifacts?
When the COVID-19 pandemic hit, there was massive investment into the discovery of new treatments. Given the urgent need, repurposing of approved or clinically pretested drugs appeared especially attractive because that strategy promised fast initiation of antiviral clinical studies. On page 541 of this issue, the study by Tummino
et al.
(
1
) raises concerns that many drug candidates that showed antiviral activity in hypothesis-free cellular screens and were then repurposed to treat severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections may be scientific dead ends. Their study is a warning that even amid the pressure of a pandemic, scientific diligence is still essential. |
doi_str_mv | 10.1126/science.abj9488 |
format | Article |
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When the COVID-19 pandemic hit, there was massive investment into the discovery of new treatments. Given the urgent need, repurposing of approved or clinically pretested drugs appeared especially attractive because that strategy promised fast initiation of antiviral clinical studies. On page 541 of this issue, the study by Tummino
et al.
(
1
) raises concerns that many drug candidates that showed antiviral activity in hypothesis-free cellular screens and were then repurposed to treat severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections may be scientific dead ends. Their study is a warning that even amid the pressure of a pandemic, scientific diligence is still essential.</description><identifier>ISSN: 0036-8075</identifier><identifier>EISSN: 1095-9203</identifier><identifier>DOI: 10.1126/science.abj9488</identifier><language>eng</language><publisher>Washington: The American Association for the Advancement of Science</publisher><subject>Antiviral activity ; Antiviral agents ; Coronaviruses ; COVID-19 ; Drug development ; Pandemics ; Severe acute respiratory syndrome ; Severe acute respiratory syndrome coronavirus 2 ; Viral diseases</subject><ispartof>Science (American Association for the Advancement of Science), 2021-07, Vol.373 (6554), p.488-489</ispartof><rights>Copyright © 2021, American Association for the Advancement of Science</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c371t-c52ce03297b39660ad9087e63f6eb14c51d5dcad1fbf58dc1078f74d62d6ab583</citedby><cites>FETCH-LOGICAL-c371t-c52ce03297b39660ad9087e63f6eb14c51d5dcad1fbf58dc1078f74d62d6ab583</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,2884,2885,27924,27925</link.rule.ids></links><search><creatorcontrib>Edwards, Aled</creatorcontrib><creatorcontrib>Hartung, Ingo V.</creatorcontrib><title>No shortcuts to SARS-CoV-2 antivirals</title><title>Science (American Association for the Advancement of Science)</title><description>Are many drug repurposers pursuing artifacts?
When the COVID-19 pandemic hit, there was massive investment into the discovery of new treatments. Given the urgent need, repurposing of approved or clinically pretested drugs appeared especially attractive because that strategy promised fast initiation of antiviral clinical studies. On page 541 of this issue, the study by Tummino
et al.
(
1
) raises concerns that many drug candidates that showed antiviral activity in hypothesis-free cellular screens and were then repurposed to treat severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections may be scientific dead ends. 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When the COVID-19 pandemic hit, there was massive investment into the discovery of new treatments. Given the urgent need, repurposing of approved or clinically pretested drugs appeared especially attractive because that strategy promised fast initiation of antiviral clinical studies. On page 541 of this issue, the study by Tummino
et al.
(
1
) raises concerns that many drug candidates that showed antiviral activity in hypothesis-free cellular screens and were then repurposed to treat severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections may be scientific dead ends. Their study is a warning that even amid the pressure of a pandemic, scientific diligence is still essential.</abstract><cop>Washington</cop><pub>The American Association for the Advancement of Science</pub><doi>10.1126/science.abj9488</doi><tpages>2</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antiviral activity Antiviral agents Coronaviruses COVID-19 Drug development Pandemics Severe acute respiratory syndrome Severe acute respiratory syndrome coronavirus 2 Viral diseases |
title | No shortcuts to SARS-CoV-2 antivirals |
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