Table 3.
Name | Developer | Clinical phase, trial identifier | Dose, regimen | Antigen coding sequence | Formulation | Clinical outcome |
---|---|---|---|---|---|---|
CVnCoV | CureVac | phase IIb/III, NCT04652102 phase I, II, NCT04449276, NCT04515147 | 12 μg, p-b, 4 weeks | full-length S, 2P | Acuitas LNP | 48% efficacy for the prevention of COVID-19 in age group 18–60 years123 |
MRT5500 (VAW00001) | Translate Bio/Sanofi | phase I/II, NCT04798027 | 7.5 μg, p-b, 3 weeks | full-length S 2P, modified furin cleavage site | LNP | not published |
ARCoV | AMS/Walvax/Suzhou | phase II, ChiCTR2100041855 | 15 μg, p-b, 2 to 4 weeks | RBD | LNP | not published |
phase III, NCT04847102 | ||||||
PTX-COVID19B | Providence Therapeutics | phase I (II), NCT04765436 | 16, 40, 100 μg, p-b, 4 weeks; 40 μg was selected for phase II | full-length S | LNP | well tolerated in seronegative 18- to 64-year-old individuals, strong IgG antibody response124 |
phase II, NCT05175742 comparison with BNT162b2 | 60, 80 μg, p-b, 4 weeks | not published | ||||
DS5670 | Daiichi Sankyo | phase I/II, NCT04821674 | dose not disclosed, p-b | not disclosed | LNP | neutralizing activity without any safety concerns in both age groups (20–64 and 65–74 years)125 |
SW-0123 | Stemirna Therapeutics/Shanghai East Hospital | phase I, ChiCTR2100045984 | 10, 30, 60, 100 μg, p-b | full-length S | LPP | not published |
EG-COVID | eyeGENE | phase I/IIa | 50, 100, 200 μg, p-b, 3 weeks | full-length S | cationic liposome | not published |
2P, two consecutive proline residues; AMS, Academy of Military Science of the Chinese People’s Liberation Army; IgG, immunoglobulin G; LNP, lipid nanoparticle; LPP, core-shell structured lipopolyplex; p-b, prime-boost regimen; RBD, receptor binding domain; S, spike protein.