An Up-to-Date Overview of Therapeutic Agents for the Treatment of COVID-19 Disease.

IF 3.1 Q2 PHARMACOLOGY & PHARMACY
Clinical Pharmacology : Advances and Applications Pub Date : 2020-12-14 eCollection Date: 2020-01-01 DOI:10.2147/CPAA.S284809
Tafere Mulaw Belete
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引用次数: 1

Abstract

Acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has a great potential to overwhelm the world healthcare systems that may lead to high morbidity and mortality. It also affects world economic development in the future. Currently, no proven effective drugs or vaccines are available for the management of COVID-19 disease. The pace of normal drug development progression is unacceptable in the context of the current pandemic. Therefore, repurposing the existing drugs that were used for the treatment of malaria, Ebola, and influenza helps rapid drug development for COVID-19. Currently, several repurposing candidate drugs are in a clinical trial including, chloroquine monoclonal antibodies, convalescent plasma, interferon, and antiviral therapies. Antiviral drugs like arbidol, remdesiv and favirnavir are the most promising due to the similarities of the viruses regarding viral entry, fusion, uncoating, and replication. This review article provides an overview of the potential therapeutic agent, which displayed better clinical treatment outcomes. Moreover, with further understanding of the SARS-CoV-2 virus, new drugs targeting specific SARS-CoV-2 viral components arise, and investigations on these novels anti-SARSCoV- 2 agents are also reviewed.

Abstract Image

COVID-19疾病治疗药物的最新概述
急性呼吸综合征冠状病毒2 (SARS-CoV-2)大流行极有可能使世界卫生系统不堪重负,从而导致高发病率和死亡率。它也影响着未来世界经济的发展。目前,没有经证实有效的药物或疫苗可用于管理COVID-19疾病。在当前大流行的背景下,正常药物开发进展的速度是不可接受的。因此,重新利用用于治疗疟疾、埃博拉和流感的现有药物有助于快速开发针对COVID-19的药物。目前,几种重新利用的候选药物正在临床试验中,包括氯喹单克隆抗体、恢复期血浆、干扰素和抗病毒治疗。抗病毒药物如阿比多尔、瑞德西夫和favirnavir是最有希望的,因为这些病毒在病毒进入、融合、脱壳和复制方面具有相似性。这篇综述文章提供了潜在的治疗药物的概述,显示出较好的临床治疗效果。此外,随着对SARS-CoV-2病毒认识的深入,针对SARS-CoV-2病毒特异性成分的新药物不断出现,并对这些新型抗sarscov -2药物的研究进展进行了综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.60
自引率
0.00%
发文量
14
审稿时长
16 weeks
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