推进非洲的疫苗研究:疫苗临床试验前景综合分析。

IF 2 3区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Lindi Mathebula, Thobile Malinga, Chinwe Iwu-Jaja, Duduzile Ndwandwe
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引用次数: 0

摘要

本研究对非洲的疫苗临床试验进行了深入分析,强调了当地投资对满足非洲大陆医疗保健需求的重要意义。研究仔细考察了非洲各国的疫苗试验,重点关注试验分布、阶段、资金来源、招募地点、招募状况和参与年龄组。研究结果表明,肯尼亚、加纳和冈比亚等国的试验活动非常活跃,而刚果民主共和国和突尼斯等国的试验活动则很少。值得注意的是,COVID-19、HIV 和黄热病疫苗在试验中占有突出地位,其中以 3 期试验最为普遍。不适用 "试验的出现表明采用了适应性试验设计。对资助模式的分析表明,国际和当地都提供了大量支持,这反映出对非洲疫苗研究的投入在不断增加。然而,试验分布和参与年龄组的差异仍然令人担忧,这凸显了建立健全的监管框架和提高当地研发能力的必要性。解决这些差距可以提高疫苗研究的效率,改善整个非洲大陆的健康状况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advancing vaccine research in Africa: A comprehensive analysis of vaccine clinical trials landscape.

This study presents an in-depth analysis of vaccine clinical trials in Africa, emphasising the significance of local investments to address the continent's healthcare requirements. The research scrutinises vaccine trials across various African nations, focusing on trial distribution, phases, funding sources, recruitment sites, recruitment statuses, and age group participation. The findings suggest substantial trial activity in countries like Kenya, Ghana, and Gambia, whereas nations like the Democratic Republic of the Congo and Tunisia exhibit minimal representation. Notably, COVID-19, HIV, and Yellow Fever vaccines prominently feature in the trials, with Phase 3 trials being the most prevalent. The presence of "Not Applicable" trials indicates adopting adaptive trial designs. Analysis of funding patterns reveals substantial international and local support, reflecting an escalating commitment to vaccine research in Africa. Nevertheless, concerns persist regarding disparities in trial distribution and age group participation, underscoring the necessity for robust regulatory frameworks and augmented local R&D capacity. Addressing these disparities can enhance the efficacy of vaccine research and elevate health outcomes across the African continent.

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来源期刊
CiteScore
3.70
自引率
4.50%
发文量
281
审稿时长
44 days
期刊介绍: Contemporary Clinical Trials is an international peer reviewed journal that publishes manuscripts pertaining to all aspects of clinical trials, including, but not limited to, design, conduct, analysis, regulation and ethics. Manuscripts submitted should appeal to a readership drawn from disciplines including medicine, biostatistics, epidemiology, computer science, management science, behavioural science, pharmaceutical science, and bioethics. Full-length papers and short communications not exceeding 1,500 words, as well as systemic reviews of clinical trials and methodologies will be published. Perspectives/commentaries on current issues and the impact of clinical trials on the practice of medicine and health policy are also welcome.
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