Table 2.
Vaccine | Developer | Route of administration/ dose | Clinical stage | Subunit and structure | Adjuvant | Efficacy | Side effects | Reference |
---|---|---|---|---|---|---|---|---|
mRNA-1273 vaccine | ModernaTX, Inc. | IM/2 | Phase 4 | LNP | No adjuvant | 100% efficacy against B.1.1.7; 95.7% efficacy against B.1.35 in Qatar and 94.1%in United States | Systemic adverse events were more common after the second vaccination. Serious adverse events were rare. |
Baden et al., 2021; Chemaitelly et al., 2021; Corbett et al., 2021 |
mRNA-1273.351 vaccine | ModernaTX, Inc. | IM/2 | Phase 2 | LNP | No adjuvant | NR | NR | Baden et al., 2021 |
BNT162b2 (Comirnaty) vaccine | Pfizer-BioNTech | IM/2 | Phase 4 | LNP | No adjuvant | 95% (based on phase 2/3) | Mild-to-moderate pain at the injection site within 7 days after injection, injection-site redness or swelling, fever, fatigue, and headache | Sahin et al., 2021 |
CVnCoV vaccine | CureVac N.V. | IM/2 | Phase 3 | LNP | No adjuvant | 48.2% (phase 2b/3) |
Injection-site pain, fatigue, headache, None of the fatal serious adverse events reported | Hoffmann et al., 2021; Kremsner et al., 2021 |
ARCoV vaccine | AMS, Walvax Biotechnology and Suzhou Abogen Bio-sciences |
IM/2 | Phase 3 | LNP | No adjuvant | NR | NR | ClinicalTrials.gov, 2021a |
mRNA-1273.211 vaccine | ModernaTX, Inc. | IM/2 | Phase 2 | LNP | No adjuvant | NR | NR | Clinicaltrials.gov, 2022b |
ARCT-154 mRNA vaccine | Arcturus Therapeutic |
IM/2 | Phase1/2/ 3 | self-amplifying mRNA | No adjuvant | NR | NR | Vietnam News Agency, n.d.; Clinical Trials Arena, 2021; ClinicalTrials.gov, 2022c |
NR: Not Reported. IM: Intramuscular. IN: Intranasal. LNP: lipid nanoparticle.