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Review of COVID-19 mRNA Vaccines: BNT162b2 and mRNA-1273
Open accessAbstract
The United States Food and Drug Administration recently issued emergency use authorization for 2 mRNA vaccines for preventing COVID-19 disease caused by SARS-CoV-2 virus infections. BNT162b2 from Pfizer-BioNTech and mRNA-1273 by Moderna are planned for use in mass-immunization programs to curb the pandemic. A brief overview of COVID-19 mRNA vaccines is provided, describing the SARS-CoV-2 RNA, how mRNA vaccines work and the advantages of mRNA over other vaccine platforms. The Pfizer-BioNTech collaboration journey to short-list mRNA vaccine candidates and finally selecting BNT162b2 based on safety data is outlined, followed by the Phase 3 study of BNT162b2 demonstrating 95% efficacy in preventing COVID-19 infections. Studies regarding mRNA-1273 (Moderna) are described, including extended immunogenicity data up to 119 days. The Phase 3 COVE study of mRNA-1273 eventually showed vaccine efficacy of 94.5%. Recommendations for future mRNA vaccine development are provided, including ongoing safety surveillance, evaluation in under-represented groups in previous studies and improving mRNA vaccine thermostability. Finally, further logistical considerations are required for manufacturing, storing, distribution and implementing mass vaccination programs to curb the pandemic.
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“with similar immune responses among adolescents aged 12 to 17.410,412–414”
From Advances in COVID-19 mRNA vaccine development (2022) · cites this paper as [413]
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“In a phase III clinical trial involving 30,420 people, participants aged 18 or older were given two doses of 100 μg of mRNA-1273 with a 28-day interval, and vaccine efficacy was 94.1% (Table 5)”
From Advances in COVID-19 mRNA vaccine development (2022) · cites this paper as [413]
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“During the phase 1, dose-escalation trial, 45 healthy adults aged 18 to 55 years were administered 2 doses of 25 mg, 100 mg or 250 mg of mRNA-1273 28 days apart.(18) In this study, there was a dose-dependent antibody response; with increasing titers and serum-neutralizing activity after the second vaccination at the u…”
MethodRNA-Based COVID-19 Vaccine BNT162b2 Selected for a Pivotal Efficacy Study
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Metadata
- Authors
- Teo, S. P.
- Affiliations
- Raja Isteri Pengiran Anak Saleha Hospital (BN)
- Corresponding author
- Teo, Shyh Poh
- ORCID
- Teo, Shyh Poh
- Venue
- Journal of Pharmacy Practice
- Publisher
- SAGE Publications
- Published
- 2021-04-12
- Volume
- 35
- Issue
- 6
- Pages
- 947-951
- ISSN
- 0897-1900 (ISSN-L)
- 1531-1937
- OpenAlex
- W3154719862
- Cited by
- 191
- References
- 26
- Citations by year
- 2026: 24 · 2025: 42 · 2024: 35 · 2023: 39 · 2022: 37 · 2021: 14
- FWCI
- 3.65
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Pharmacy Practice (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
- Health Sciences › Medicine › Infectious Diseases › COVID-19 Clinical Research Studies
- Social Sciences › Health › Vaccine Coverage and Hesitancy
- Keywords
- COVID-19 mRNA vaccine, BNT162b2, mRNA-1273, SARS-CoV-2, vaccine development, vaccine efficacy, immunogenicity, vaccine safety, emergency use authorization, vaccine thermostability, underrepresented groups
- MeSH terms
- COVID-19, SARS-CoV-2, COVID-19 Vaccines, mRNA Vaccines, BNT162 Vaccine, 2019-nCoV Vaccine mRNA-1273, Humans, RNA, Viral, United States, Viral Vaccines
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