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战胜困难:在有史以来最大规模的埃博拉疫情期间,于资源匮乏的利比里亚成功开展一项II/III期临床研究试验。

Beating the Odds: Successful Establishment of a Phase II/III Clinical Research Trial in Resource-Poor Liberia during the Largest-Ever Ebola Outbreak.

作者信息

Doe-Anderson J, Baseler B, Driscoll P, Johnson M, Lysander J, McNay L, Njoh W S, Smolskis M, Wehrlen L, Zuckerman J

机构信息

Clinical Research Directorate/Clinical Monitoring Research Program, Leidos Biomedical Research, Inc., NCI Campus at Frederick, Frederick, MD, 21702, USA.

Intramural Clinical Management and Operations Branch, National Institute of Allergy and Infectious Diseases, Rockville, MD, USA.

出版信息

Contemp Clin Trials Commun. 2016 Dec 15;4:68-73. doi: 10.1016/j.conctc.2016.06.008. Epub 2016 Jun 24.

Abstract

It has been argued that a country such as Liberia, not fully recovered from the devastation of decades of civil unrest, lacked the appropriate ethical and regulatory framework, basic human and health care services, and infrastructure to carry out clinical trials according to international standards of quality during a public health emergency. However, as Liberia, Sierra Leone, and Guinea were being ravaged by the largest and most devastating Ebola Virus Disease (EVD) outbreak ever recorded, the topic of conducting clinical trials of experimental vaccine and treatment candidates in these resource-poor countries generated the keen interest and concern of scientists, researchers, physicians, bioethicists, philanthropists, and even politicians. Decisive action on behalf of the Liberian government, and a timely positive and supportive response from the United States (U.S.) government, led to the formation of PREVAIL (Partnership for Research on Ebola Vaccines in Liberia) - a clinical research partnership between the two governments. Within a span of 12 weeks, this partnership accomplished the unimaginable: the successful initiation of a Phase II/III vaccine clinical trial for EVD in Liberia. This paper will discuss the dynamics of the research collaboration, barriers encountered, breakthroughs realized, key elements of success, and lessons learned in the process.

摘要

有人认为,像利比里亚这样尚未从数十年内乱的破坏中完全恢复的国家,缺乏适当的伦理和监管框架、基本的人力和医疗服务以及基础设施,无法在公共卫生紧急情况下按照国际质量标准开展临床试验。然而,当利比里亚、塞拉利昂和几内亚遭受有史以来最大规模、最具毁灭性的埃博拉病毒病(EVD)疫情肆虐时,在这些资源匮乏的国家开展实验性疫苗和治疗候选药物临床试验的话题引起了科学家、研究人员、医生、生物伦理学家、慈善家甚至政治家的浓厚兴趣和关注。利比里亚政府采取的果断行动以及美国政府及时给予的积极支持回应,促成了PREVAIL(利比里亚埃博拉疫苗研究伙伴关系)的形成——这是两国政府之间的临床研究伙伴关系。在短短12周内,这一伙伴关系取得了令人难以想象的成果:在利比里亚成功启动了针对埃博拉病毒病的II/III期疫苗临床试验。本文将讨论研究合作的动态情况、遇到的障碍、取得的突破、成功的关键要素以及在此过程中吸取的经验教训。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1f1/5935884/0bda181d478e/gr1.jpg

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