Vaccines in clinical use/phase III trial, their routes of administration, dose, immunogenicity, safety profile, and authorized country
Vaccine | Vaccine platform | Immunogen | Dosage | Route | Interval | Efficacy | Overall efficacy | Current EUA |
---|---|---|---|---|---|---|---|---|
BNT162b2 Pfizer-BioNTech (US) [81–86] | mRNA | SP | 30 μg, 2 doses | IM | 21 days | 88.9% after 1st dose | 52% after 1st dose; 94.6% after 7 days of 2nd dose | US, EU, Canada, and UK |
mRNA-1273 Moderna (US) [87–89] | mRNA | SP | 100 μg, 2 doses | IM | 28 days | 100% after 14 days of 2nd dose | 92.1% after 14 days of 1st dose; 94.1% after 14 days of 2nd dose | US, EU, Canada, and UK |
Ad26.CoV2.S Janssen/Johnson & Johnson (US) [90, 91] | Recombinant, replication incompetent human adenovirus serotype 26 vector | SP | 5×1010 viral particles, single dose | IM | - | 85% after 28 days; 100% after 49 days | 72% in the US; 66% in Latin America; 57% in South Africa (at 28 day) | US, EU, and Canada |
ChAdOx1 (AZS1222) AstraZeneca/Oxford (UK) [92–94] | Replication deficient chimpanzee adenoviral vector | SP | 5×1010 viral particles, 2 doses | IM | 4 to 12 weeks | 100% after 21 days of 1st dose | 64.1% after 1st dose; 70.4% after 14 days of 2nd dose | UK, WHO/Covax, India, and Mexico |
Gam-COVID-Vac (Sputnik V) [97] | Recombinant adenovirus | GS | 1011 viral particles, 2 doses | IM | 21 days | 100% after 21 days of 1st dose | 87.6% after 14 days of 1st dose; 91.1% after 7 days of 2nd dose | Russia, Belarus, Argentina, Serbia, Egypt, Algeria, UAE, and Palestine |
Covaxin (BBV152; Bharat Biotech and Ocugen) [98] | Whole-virion inactivated | SP | 6 μg of whole virions, 2 doses | IM | 4 weeks | 81% (phase III interim results) after 2nd dose | - | India |
GS: glycoprotein spike; SP: spike protein; IM: intramuscular; EUA: Emergency Use Authorization
MG and MM: conception, drafting, organizing, revision, and final approval of the manuscript; SG, VS and IPS: drafting, organizing, revision, and final approval of the manuscript; HB: illustrations, drafting, revision, and final approval of the manuscript; YK: drafting, organizing, revision, and final approval of the manuscript.
The authors declare that they have no conflicts of interest.
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© The Author(s) 2021.