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Efficacy and Safety of Triazavirin Therapy for Coronavirus Disease 2019: A Pilot Randomized Controlled Trial
No therapeutics have been proven effective yet for the treatment of coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). To assess the efficacy and safety of Triazavirin therapy for COVID-19, we conducted a randomized, double-blinded controlled...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
THE AUTHORS. Published by Elsevier LTD on behalf of Chinese Academy of Engineering and Higher Education Press Limited Company.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7476906/ https://www.ncbi.nlm.nih.gov/pubmed/32923016 http://dx.doi.org/10.1016/j.eng.2020.08.011 |
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author | Wu, Xiaoke Yu, Kaijiang Wang, Yongchen Xu, Wanhai Ma, Hongli Hou, Yan Li, Yue Cai, Benzhi Zhu, Liying Zhang, Min Hu, Xiaoli Gao, Jingshu Wang, Yu Qin, Huichao Wang, Wenjie Zhao, Mingyan Wu, Xia Zhang, Yong Li, Lu Li, Kang Du, Zhimin Mol, Ben Willem J. Yang, Baofeng |
author_facet | Wu, Xiaoke Yu, Kaijiang Wang, Yongchen Xu, Wanhai Ma, Hongli Hou, Yan Li, Yue Cai, Benzhi Zhu, Liying Zhang, Min Hu, Xiaoli Gao, Jingshu Wang, Yu Qin, Huichao Wang, Wenjie Zhao, Mingyan Wu, Xia Zhang, Yong Li, Lu Li, Kang Du, Zhimin Mol, Ben Willem J. Yang, Baofeng |
author_sort | Wu, Xiaoke |
collection | PubMed |
description | No therapeutics have been proven effective yet for the treatment of coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). To assess the efficacy and safety of Triazavirin therapy for COVID-19, we conducted a randomized, double-blinded controlled trial involving hospitalized adult patients with COVID-19. Participants were enrolled from ten sites, and were randomized into two arms of the study with a ratio of 1:1. Patients were treated with Triazavirin 250 mg versus a placebo three or four times a day for 7 d. The primary outcome was set as the time to clinical improvement, defined as normalization of body temperature, respiratory rate, oxygen saturation, cough, and absorption of pulmonary infection by chest computed tomography (CT) until 28 d after randomization. Secondary outcomes included individual components of the primary outcome, the mean time and proportion of inflammatory absorption in the lung, and the conversion rate to a repeated negative SARS-CoV-2 nucleic acid test of throat swab sampling. Concomitant therapeutic treatments, adverse events, and serious adverse events were recorded. Our study was halted after the recruitment of 52 patients, since the number of new infections in the participating hospitals decreased greatly. We randomized 52 patients for treatment with Triazavirin (n = 26) or a placebo (n = 26). We found no differences in the time to clinical improvement (median, 7 d versus 12 d; risk ratio (RR), 2.0; 95% confidence interval (CI), 0.7–5.6; p = 0.2), with clinical improvement occurring in ten patients in the Triazavirin group and six patients in the placebo group (38.5% versus 23.1%; RR, 2.1; 95% CI, 0.6–7.0; p = 0.2). All components of the primary outcome normalized within 28 d, with the exception of absorption of pulmonary infection (Triazavirin 50.0%, placebo 26.1%). Patients in the Triazavirin group used less frequent concomitant therapies for respiratory, cardiac, renal, hepatic, or coagulation supports. Although no statistically significant evidence was found to indicate that Triazavirin benefits COVID-19 patients, our observations indicated possible benefits from its use to treat COVID-19 due to its antiviral effects. Further study is required for confirmation. |
format | Online Article Text |
id | pubmed-7476906 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | THE AUTHORS. Published by Elsevier LTD on behalf of Chinese Academy of Engineering and Higher Education Press Limited Company. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74769062020-09-08 Efficacy and Safety of Triazavirin Therapy for Coronavirus Disease 2019: A Pilot Randomized Controlled Trial Wu, Xiaoke Yu, Kaijiang Wang, Yongchen Xu, Wanhai Ma, Hongli Hou, Yan Li, Yue Cai, Benzhi Zhu, Liying Zhang, Min Hu, Xiaoli Gao, Jingshu Wang, Yu Qin, Huichao Wang, Wenjie Zhao, Mingyan Wu, Xia Zhang, Yong Li, Lu Li, Kang Du, Zhimin Mol, Ben Willem J. Yang, Baofeng Engineering (Beijing) Research Coronavirus Disease 2019—Article No therapeutics have been proven effective yet for the treatment of coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). To assess the efficacy and safety of Triazavirin therapy for COVID-19, we conducted a randomized, double-blinded controlled trial involving hospitalized adult patients with COVID-19. Participants were enrolled from ten sites, and were randomized into two arms of the study with a ratio of 1:1. Patients were treated with Triazavirin 250 mg versus a placebo three or four times a day for 7 d. The primary outcome was set as the time to clinical improvement, defined as normalization of body temperature, respiratory rate, oxygen saturation, cough, and absorption of pulmonary infection by chest computed tomography (CT) until 28 d after randomization. Secondary outcomes included individual components of the primary outcome, the mean time and proportion of inflammatory absorption in the lung, and the conversion rate to a repeated negative SARS-CoV-2 nucleic acid test of throat swab sampling. Concomitant therapeutic treatments, adverse events, and serious adverse events were recorded. Our study was halted after the recruitment of 52 patients, since the number of new infections in the participating hospitals decreased greatly. We randomized 52 patients for treatment with Triazavirin (n = 26) or a placebo (n = 26). We found no differences in the time to clinical improvement (median, 7 d versus 12 d; risk ratio (RR), 2.0; 95% confidence interval (CI), 0.7–5.6; p = 0.2), with clinical improvement occurring in ten patients in the Triazavirin group and six patients in the placebo group (38.5% versus 23.1%; RR, 2.1; 95% CI, 0.6–7.0; p = 0.2). All components of the primary outcome normalized within 28 d, with the exception of absorption of pulmonary infection (Triazavirin 50.0%, placebo 26.1%). Patients in the Triazavirin group used less frequent concomitant therapies for respiratory, cardiac, renal, hepatic, or coagulation supports. Although no statistically significant evidence was found to indicate that Triazavirin benefits COVID-19 patients, our observations indicated possible benefits from its use to treat COVID-19 due to its antiviral effects. Further study is required for confirmation. THE AUTHORS. Published by Elsevier LTD on behalf of Chinese Academy of Engineering and Higher Education Press Limited Company. 2020-10 2020-09-08 /pmc/articles/PMC7476906/ /pubmed/32923016 http://dx.doi.org/10.1016/j.eng.2020.08.011 Text en © 2020 THE AUTHORS. Published by Elsevier LTD on behalf of Chinese Academy of Engineering and Higher Education Press Limited Company. 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 | Research Coronavirus Disease 2019—Article Wu, Xiaoke Yu, Kaijiang Wang, Yongchen Xu, Wanhai Ma, Hongli Hou, Yan Li, Yue Cai, Benzhi Zhu, Liying Zhang, Min Hu, Xiaoli Gao, Jingshu Wang, Yu Qin, Huichao Wang, Wenjie Zhao, Mingyan Wu, Xia Zhang, Yong Li, Lu Li, Kang Du, Zhimin Mol, Ben Willem J. Yang, Baofeng Efficacy and Safety of Triazavirin Therapy for Coronavirus Disease 2019: A Pilot Randomized Controlled Trial |
title | Efficacy and Safety of Triazavirin Therapy for Coronavirus Disease 2019: A Pilot Randomized Controlled Trial |
title_full | Efficacy and Safety of Triazavirin Therapy for Coronavirus Disease 2019: A Pilot Randomized Controlled Trial |
title_fullStr | Efficacy and Safety of Triazavirin Therapy for Coronavirus Disease 2019: A Pilot Randomized Controlled Trial |
title_full_unstemmed | Efficacy and Safety of Triazavirin Therapy for Coronavirus Disease 2019: A Pilot Randomized Controlled Trial |
title_short | Efficacy and Safety of Triazavirin Therapy for Coronavirus Disease 2019: A Pilot Randomized Controlled Trial |
title_sort | efficacy and safety of triazavirin therapy for coronavirus disease 2019: a pilot randomized controlled trial |
topic | Research Coronavirus Disease 2019—Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7476906/ https://www.ncbi.nlm.nih.gov/pubmed/32923016 http://dx.doi.org/10.1016/j.eng.2020.08.011 |
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