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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

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...

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Detalles Bibliográficos
Autores principales: Sathian, Brijesh, Asim, Mohammad, Banerjee, Indrajit, Roy, Bedanta, Pizarro, Ana Beatriz, Mancha, Maraeh Angela, van Teijlingen, Edwin R., Kord-Varkaneh, Hamed, Mekkodathil, Ahammed A, Subramanya, Supram Hosuru, Borges do Nascimento, Israel Júnior, Antony, Neema, Menezes, Ritesh G, Simkhada, Padam, Al Hamad, Hanadi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Nepal Epidemiological Association 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8033643/
https://www.ncbi.nlm.nih.gov/pubmed/33868742
http://dx.doi.org/10.3126/nje.v11i1.36163
Descripción
Sumario: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.