1 London School of Hygiene & Tropical Medicine, London, UK.
2 College of Medicine and Allied Health Sciences, University of Sierra Leone, Freetown, Sierra Leone.
Clin Trials. 2018 Oct;15(5):436-443. doi: 10.1177/1740774518780678. Epub 2018 Jun 12.
Background/aims During the 2014-2016 West African Ebola epidemic, clinical trials were fast-tracked in order to identify prophylactic vaccines and experimental treatments that might be useful in preventing or treating Ebola. These trials included the ongoing EBOVAC-Salone study, which was established and implemented in Sierra Leone to assess the safety and immunogenicity of the Ad26.ZEBOV/MVA-BN-Filo prime-boost Ebola vaccine regimen. Methods This article describes the experiences of the EBOVAC-Salone research team in setting up and implementing the trial, and provides recommendations for research teams aiming to conduct clinical trials in future outbreak situations. Results Establishing a clinical trial during an outbreak brought some unique challenges, including those related to trial design and the regulatory environment, operational issues, and community engagement. The situation was further complicated by the weak infrastructure and limited experience of clinical trials in Sierra Leone. However, operating in an outbreak context also brought some benefits to the research team, including strong stakeholder support. The EBOVAC-Salone study recruited participants both during and after the outbreak, leading to additional challenges to trial implementation during the post-outbreak transition. Conclusion Many lessons have been learned about setting up and implementing a clinical trial during a devastating Ebola epidemic, and some of the experiences of the EBOVAC-Salone team were mirrored by those of other researchers operating in the region. Common to several of these research groups is a recommendation that research should be more closely incorporated into outbreak response planning, which could expedite the establishment of timely and appropriate research projects. We recommend that the lessons learned by researchers during the West African Ebola epidemic are built into programmes and strategies to improve the responses to future epidemics, wherever they occur.
背景/目的:在 2014-2016 年西非埃博拉疫情期间,为了确定可能有助于预防或治疗埃博拉的预防性疫苗和实验性治疗方法,加快了临床试验的进程。这些试验包括正在进行的 EBOVAC-Salone 研究,该研究在塞拉利昂成立并实施,以评估 Ad26.ZEBOV/MVA-BN-Filo 疫苗方案的安全性和免疫原性。
本文描述了 EBOVAC-Salone 研究团队在建立和实施试验方面的经验,并为旨在在未来疫情情况下开展临床试验的研究团队提供了建议。
在疫情期间建立临床试验带来了一些独特的挑战,包括与试验设计和监管环境、运营问题和社区参与有关的挑战。塞拉利昂临床试验基础设施薄弱和经验有限,使情况更加复杂。然而,在疫情环境下运作也为研究团队带来了一些好处,包括利益相关者的大力支持。EBOVAC-Salone 研究在疫情期间和疫情后都招募了参与者,这导致了疫情后过渡期间试验实施的额外挑战。
在毁灭性的埃博拉疫情期间设立和实施临床试验方面吸取了许多经验教训,EBOVAC-Salone 研究团队的一些经验与该地区其他研究人员的经验相呼应。这些研究小组的共同建议是,应更密切地将研究纳入疫情应对规划,这可以加快及时和适当的研究项目的建立。我们建议,在西非埃博拉疫情期间研究人员吸取的经验教训应纳入方案和战略,以改善对未来任何地方发生的疫情的应对。