Vaccines in clinical use/phase III trial, their routes of administration, dose, immunogenicity, safety profile, and authorized country

VaccineVaccine platformImmunogenDosageRouteIntervalEfficacyOverall efficacyCurrent EUA
BNT162b2 Pfizer-BioNTech (US) [8186]mRNASP30 μg, 2 dosesIM21 days88.9% after 1st dose52% after 1st dose; 94.6% after 7 days of 2nd doseUS, EU, Canada, and UK
mRNA-1273 Moderna (US) [8789]mRNASP100 μg, 2 dosesIM28 days100% after 14 days of 2nd dose92.1% after 14 days of 1st dose; 94.1% after 14 days of 2nd doseUS, EU, Canada, and UK
Ad26.CoV2.S Janssen/Johnson & Johnson (US) [90, 91]Recombinant, replication incompetent human adenovirus serotype 26 vectorSP5×1010 viral particles, single doseIM-85% after 28 days; 100% after 49 days72% in the US; 66% in Latin America; 57% in South Africa (at 28 day)US, EU, and Canada
ChAdOx1 (AZS1222) AstraZeneca/Oxford (UK) [9294]Replication deficient chimpanzee adenoviral vectorSP5×1010 viral particles, 2 dosesIM4 to 12 weeks100% after 21 days of 1st dose64.1% after 1st dose; 70.4% after 14 days of 2nd doseUK, WHO/Covax, India, and Mexico
Gam-COVID-Vac (Sputnik V) [97]Recombinant adenovirusGS1011 viral particles, 2 dosesIM21 days100% after 21 days of 1st dose87.6% after 14 days of 1st dose; 91.1% after 7 days of 2nd doseRussia, Belarus, Argentina, Serbia, Egypt, Algeria, UAE, and Palestine
Covaxin (BBV152; Bharat Biotech and Ocugen) [98]Whole-virion inactivatedSP6 μg of whole virions, 2 dosesIM4 weeks81% (phase III interim results) after 2nd dose-India

GS: glycoprotein spike; SP: spike protein; IM: intramuscular; EUA: Emergency Use Authorization