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. 2023 Jan 19;14:331. doi: 10.1038/s41467-022-35768-3

Table 3.

Comparison of correlation of risk results for spike IgG and PsV-nAb ID50 across three randomized, placebo-controlled COVID-19 vaccine efficacy trials (U.S. study sites)

Vaccine Platforma Trial Ab Marker at 2 or 4 Wksb Post-Vaccination Follow-Up Post Vaccination Estimated Hazard Ratio per 10-fold Increase in the Marker (95% CI) P Value Q Value FWER-Adjusted P Value
mRNA COVE Spike IgG 126 days 0.66 (0.50, 0.88) 0.005 0.014 0.010
Ad26 ENSEMBLE-U.S. Spike IgG 83 days 0.62 (0.28, 1.37) 0.24 0.35 0.36
Recombinant Protein PREVENT-19 Spike IgG 73 days 0.36 (0.20, 0.64) <0.001 0.005 0.005
mRNA COVE RBD IgG 126 days 0.57 (0.40, 0.82) 0.002 0.008 0.008
Ad26 ENSEMBLE-U.S. RBD IgG 83 days 0.50 (0.21, 1.21) 0.13 0.24 0.22
Recombinant Protein PREVENT-19 RBD IgG 73 days 0.35 (0.18, 0.69) 0.002 0.012 0.013
mRNA COVE PsV-nAb ID50 126 days 0.42 (0.27, 0.65) <0.001 0.002 0.003
Ad26 ENSEMBLE-U.S. PsV-nAb ID50 83 days 0.38 (0.13, 1.12) 0.078 0.22 0.20
Recombinant Protein PREVENT-19 PsV-nAb ID50 73 days 0.39 (0.19, 0.82) 0.013 0.032 0.030

aCOVE: Moderna mRNA-1273 spike vaccine; ENSEMBLE: Janssen Ad26 vector spike vaccine Ad26.CoV2.S; PREVENT-19: Novavax recombinant spike protein vaccine NVX-CoV2373.

bIn COVE and ENSEMBLE, the antibody markers were measured 4 weeks post-vaccination, compared to 2 weeks post-vaccination in PREVENT-19.