新冠肺炎影响下药物一期临床试验受试者管理的思考

T. Zhao
{"title":"新冠肺炎影响下药物一期临床试验受试者管理的思考","authors":"T. Zhao","doi":"10.7501/j.issn.1674-6376.2020.11.034","DOIUrl":null,"url":null,"abstract":"Since the end of 2019, the spread of the corona virus disease 2019 (COVID-19) has caused serious economic shocks and social impacts. The development of clinical trials of drugs has also brought many difficulties and challenges. Based on the particularity of the population and process of the Phase I clinical trials of the drug, it caused us to think about the management of the subjects in the Phase I clinical trials under the influence of the COVID-19. It proposes various strategies from the different stages of subject recruitment, screening, and admission, to subject education, diet management, and observation of adverse events. It aims to discuss how to protect the safety and rights of subjects better under the normalization of epidemic prevention and control, strengthen the risk control of clinical trials, and ensure the successful completion of trials.","PeriodicalId":11302,"journal":{"name":"药物评价研究","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2020-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Reflections on management of subjects in phase I clinical trials of drugs under influence of COVID-19\",\"authors\":\"T. Zhao\",\"doi\":\"10.7501/j.issn.1674-6376.2020.11.034\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Since the end of 2019, the spread of the corona virus disease 2019 (COVID-19) has caused serious economic shocks and social impacts. The development of clinical trials of drugs has also brought many difficulties and challenges. Based on the particularity of the population and process of the Phase I clinical trials of the drug, it caused us to think about the management of the subjects in the Phase I clinical trials under the influence of the COVID-19. It proposes various strategies from the different stages of subject recruitment, screening, and admission, to subject education, diet management, and observation of adverse events. It aims to discuss how to protect the safety and rights of subjects better under the normalization of epidemic prevention and control, strengthen the risk control of clinical trials, and ensure the successful completion of trials.\",\"PeriodicalId\":11302,\"journal\":{\"name\":\"药物评价研究\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"药物评价研究\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.7501/j.issn.1674-6376.2020.11.034\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"药物评价研究","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.7501/j.issn.1674-6376.2020.11.034","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

2019年底以来,2019冠状病毒病(COVID-19)的传播造成了严重的经济冲击和社会影响。药物临床试验的开展也带来了许多困难和挑战。基于该药物一期临床试验人群和过程的特殊性,引起我们对新冠肺炎影响下一期临床试验受试者管理的思考。它提出了从受试者招募、筛选和入院的不同阶段,到受试者教育、饮食管理和不良事件观察的各种策略。旨在探讨在疫情防控常态化的背景下,如何更好地保障受试者的安全和权益,加强临床试验的风险控制,确保临床试验的顺利完成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Reflections on management of subjects in phase I clinical trials of drugs under influence of COVID-19
Since the end of 2019, the spread of the corona virus disease 2019 (COVID-19) has caused serious economic shocks and social impacts. The development of clinical trials of drugs has also brought many difficulties and challenges. Based on the particularity of the population and process of the Phase I clinical trials of the drug, it caused us to think about the management of the subjects in the Phase I clinical trials under the influence of the COVID-19. It proposes various strategies from the different stages of subject recruitment, screening, and admission, to subject education, diet management, and observation of adverse events. It aims to discuss how to protect the safety and rights of subjects better under the normalization of epidemic prevention and control, strengthen the risk control of clinical trials, and ensure the successful completion of trials.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
0.50
自引率
0.00%
发文量
3345
期刊介绍:
期刊最新文献
Patent information analysis on traditional Chinese medicine for prevention and treatment of COVID-19 Investigated potential traditional Chinese medicinal ingredients in treatment on COVID-19 based on database Reflections on management of subjects in phase I clinical trials of drugs under influence of COVID-19 Introduction of FDA guidance for dealing with drug shortage in public health emergency Introduction of EU guideline on optimal and rational supply of medicines in public health emergency
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1