基于血浆免疫球蛋白和单克隆抗体的药品治疗和预防COVID-19的疗效

Q4 Immunology and Microbiology
A. Soldatov, Z. Avdeeva, D. Gorenkov, L. M. Khantimirova, Yu.S. Paramonova, E.M. Smolina, V. Bondarev, V. A. Merkulov
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引用次数: 3

摘要

COVID-19大流行的发展开启了寻找治疗和预防感染的有效药物的进程。在防治这一流行病的斗争中,特别重要的是将药物引入临床实践的时机。因此,医疗体系发达的国家(欧盟、美国、俄罗斯联邦等)根据紧急情况下药品流通的监管要求,发布了治疗和预防COVID-19药物的有条件上市许可。批准是在有限的临床数据基础上发出的,条件是在注册后期间授权发布后将进行充分的安全性和有效性评估。COVID-19大流行彻底改变了临床试验的设计和时间框架,包括I期、II期和III期适应性试验,这使得大多数先进制药国家以创纪录的时间批准了用于治疗和预防COVID-19的生物制剂。与此同时,监管/保健当局或国际组织不断监测使用药物的安全性和有效性,并在必要时进行调整(改变使用适应症、改变剂量、停药等)。事实上,自大流行开始以来,在允许根据非常有限的数据使用药物的情况下,研究已经开始证实使用免疫球蛋白制剂和单克隆抗体治疗和预防COVID-19的安全性和有效性。随着获得新数据,用于治疗和预防COVID-19的免疫球蛋白和单克隆抗体制剂的使用适应症、剂量和其他特性发生了变化。本综述对大流行期间使用免疫球蛋白制剂和单克隆抗体的安全性和有效性评价结果进行了批判性分析。版权所有©2022新浪传媒出版社。版权所有。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The efficacy of medicinal products based on plasma immunoglobulins and monoclonal antibodies for the treatment and prevention of COVID-19
The development of the COVID-19 pandemic initiated the search for effective drugs for the treatment and prevention of infection. Of particular importance for the fight against the pandemic is the timing of the introduction of drugs into clinical practice. Therefore, countries with developed healthcare systems (EU, USA, Russian Federation, etc.), issue conditional marketing authorizations of drugs for treatment and prevention of COVID-19, based on regulatory requirements for the circulation of medicines in emergency situations. The approval is issued on the basis of limited clinical data, with the condition that the full evaluation of safety and effectiveness will be carried out after the issuance of the authorization in the post-registration period. The COVID-19 pandemic has revolutionized the design and time frame of clinical trials, including phase I, II, and III adaptive trials, which has led to the approval of biologics for the treatment and prevention of COVID-19 in record time in most advanced pharmaceutical countries. At the same time, regulatory/healthcare authorities or international organizations constantly monitor the safety and effectiveness of used drugs and, if necessary, make adjustments (changes to the indications for use, dosage change, drug discontinuation etc.). Since the beginning of the pandemic, in fact, in conditions where the use of medicines was allowed based on very limited data, studies have begun to substantiate the safety and effectiveness of the use of immunoglobulin preparations and monoclonal antibodies for the treatment and prevention of COVID-19. As new data became available, changes were made regarding the indications for use, doses, and other characteristics of preparations of immunoglobulins and monoclonal antibodies for the treatment and prevention of COVID-19. The review presents a critical analysis of the results of evaluation the safety and effectiveness of the use of immunoglobulin preparations and monoclonal antibodies in a pandemic. Copyright © 2022 Meditsina Publishers. All rights reserved.
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来源期刊
Immunologiya
Immunologiya Immunology and Microbiology-Immunology
CiteScore
1.90
自引率
0.00%
发文量
31
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