日本的临床试验经验和未来开发治疗COVID-19药物的问题。

IF 1.9 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Ayako Mikami, Junko Terada-Hirashima, Daisuke Tokita, Wataru Sugiura
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引用次数: 0

摘要

国家全球卫生和医学中心在日本传染病的治疗和研究方面发挥着核心作用。以临床问题为切入点,开展了多种新型冠状病毒病(COVID-19)治疗药物研发活动。临床试验是发展新治疗方式的必要条件,但我们注意到在新发和再发传染病的临床试验中存在一些特征性困难。例如,当一种新出现的传染病开始传播时,由于没有护理标准,因此建立一个适当的对照组是复杂的,而且在试验开始时许多事情都很匆忙。这意味着几乎没有时间安排安慰剂,而且进行盲法、随机对照试验一直很困难。传染病的另一个特点是,在招募受试者方面的进展受到疾病传播的影响。选择在传染病第一线提供医疗服务并定期进行临床试验的机构也是一场斗争。因此,为了迅速开展多中心临床试验,一个规范和结构化的网络被认为是必要的。从实施的角度来看,开展不依赖于人来医疗机构的分散式临床试验(dct)是可取的,而从COVID-19传播期间预防感染的角度来看,广泛采用eConsent是可取的。根据2019冠状病毒病的经验,必须采取新的措施,为未来新发和再发传染病做好准备。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical trial experience in Japan and future issues in developing drugs to treat COVID-19.

The National Center for Global Health and Medicine plays a central role in the treatment and research of infectious diseases in Japan. It has conducted various research and development activities on drugs to treat coronavirus disease 2019 (COVID-19) with clinical questions as starting points. Clinical trials are essential in developing new treatment modalities, but we have noticed some characteristic difficulties in clinical trials on emerging and re-emerging infectious diseases. For example, since there is no standard of care when an emerging infectious disease starts to spread, establishing an appropriate control group is complicated, and many things are hurried at the start of trials. This means there is little time to arrange a placebo, and conducting blinded, randomized, controlled trials has been difficult. Another issue characteristic of infectious disease has been that progress in enrolling subjects is affected by the spread of the disease. It was also a struggle to select institutions that provide medical care on the front lines of infectious disease and conduct clinical trials regularly. To start multicenter clinical trials expeditiously, a regulated and structured network is thus considered necessary. From the perspective of implementation, it is preferable to conduct decentralized clinical trials (DCTs) that do not depend on people coming to the medical institution, while from the perspective of preventing infections during the spread of COVID-19, wide adoption of eConsent is desirable. Based on the experience of COVID-19, new measures must be taken to prepare for emerging and re-emerging infectious diseases in the future.

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