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Development and implementation of a potential coronavirus disease 2019 (COVID-19) vaccine: A systematic review and meta-analysis of vaccine clinical trials

机译:潜在冠状病毒疾病2019(Covid-19)疫苗的开发和实施:系统审查和疫苗临床试验的荟萃分析

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Background: To date, there is no comprehensive systematic review and meta-analysis to assess the suitability of COVID-19 vaccines for mass immunization. The current systematic review and meta-analysis was conducted to evaluate the safety and immunogenicity of novel COVID-19 vaccine candidates under clinical trial evaluation and present a contemporary update on the development and implementation of a potential vaccines. Methods: For this study PubMed, MEDLINE, and Embase electronic databases were used to search for eligible studies on the interface between novel coronavirus and vaccine design until December 31, 2020. Results: We have included fourteen non-randomized and randomized controlled phase I-III trials. Implementation of a universal vaccination program with proven safety and efficacy through robust clinical evaluation is the long-term goal for preventing COVID-19. The immunization program must be cost-effective for mass production and accessibility. Despite pioneering techniques for the fast-track development of the vaccine in the current global emergency, mass production and availability of an effective COVID-19 vaccine could take some more time. Conclusion: Our findings suggest a revisiting of the reported solicited and unsolicited systemic adverse events for COVID-19 candidate vaccines. Hence, it is alarming to judiciously expose thousands of participants to COVID-19 candidate vaccines at Phase-3 trials that have adverse events and insufficient evidence on safety and effectiveness that necessitates further justification.
机译:背景:迄今为止,没有全面的系统审查和荟萃分析,以评估Covid-19疫苗进行大规模免疫的适用性。目前进行了系统审查和荟萃分析,以评估临床试验评估下新型Covid-19疫苗候选者的安全性和免疫原性,并提出了一种关于潜在疫苗的开发和实施的当代更新。方法:对于本研究,用于搜索新型冠状病毒和疫苗设计之间的界面的符合条件的研究,直到2020年12月31日,我们研究了符合条件的研究。结果:我们已经包括十四个非随机和随机对照阶段I- III试验。通过稳健的临床评估实现普遍疫苗接种计划,通过稳健的临床评估是预防Covid-19的长期目标。免疫计划必须对批量生产和可访问性具有成本效益。尽管在目前全球紧急情况下,疫苗的快速发展技术开创了技术,但有效的Covid-19疫苗的批量生产和可用性可能需要更多时间。结论:我们的研究结果表明,重新审查了Covid-19候选疫苗的报告征集和未经请求的全身不良事件。因此,在阶段3试验中明智地将数千名参与者促使成千上万的参与者令人震惊,这些疫苗具有不良事件,并且有关需要进一步理由的安全性和有效性的证据不足。

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