Back to Search Start Over

Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine.

Authors :
Polack FP
Thomas SJ
Kitchin N
Absalon J
Gurtman A
Lockhart S
Perez JL
Pérez Marc G
Moreira ED
Zerbini C
Bailey R
Swanson KA
Roychoudhury S
Koury K
Li P
Kalina WV
Cooper D
Frenck RW Jr
Hammitt LL
Türeci Ö
Nell H
Schaefer A
Ünal S
Tresnan DB
Mather S
Dormitzer PR
Şahin U
Jansen KU
Gruber WC
Source :
The New England journal of medicine [N Engl J Med] 2020 Dec 31; Vol. 383 (27), pp. 2603-2615. Date of Electronic Publication: 2020 Dec 10.
Publication Year :
2020

Abstract

Background: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and the resulting coronavirus disease 2019 (Covid-19) have afflicted tens of millions of people in a worldwide pandemic. Safe and effective vaccines are needed urgently.<br />Methods: In an ongoing multinational, placebo-controlled, observer-blinded, pivotal efficacy trial, we randomly assigned persons 16 years of age or older in a 1:1 ratio to receive two doses, 21 days apart, of either placebo or the BNT162b2 vaccine candidate (30 μg per dose). BNT162b2 is a lipid nanoparticle-formulated, nucleoside-modified RNA vaccine that encodes a prefusion stabilized, membrane-anchored SARS-CoV-2 full-length spike protein. The primary end points were efficacy of the vaccine against laboratory-confirmed Covid-19 and safety.<br />Results: A total of 43,548 participants underwent randomization, of whom 43,448 received injections: 21,720 with BNT162b2 and 21,728 with placebo. There were 8 cases of Covid-19 with onset at least 7 days after the second dose among participants assigned to receive BNT162b2 and 162 cases among those assigned to placebo; BNT162b2 was 95% effective in preventing Covid-19 (95% credible interval, 90.3 to 97.6). Similar vaccine efficacy (generally 90 to 100%) was observed across subgroups defined by age, sex, race, ethnicity, baseline body-mass index, and the presence of coexisting conditions. Among 10 cases of severe Covid-19 with onset after the first dose, 9 occurred in placebo recipients and 1 in a BNT162b2 recipient. The safety profile of BNT162b2 was characterized by short-term, mild-to-moderate pain at the injection site, fatigue, and headache. The incidence of serious adverse events was low and was similar in the vaccine and placebo groups.<br />Conclusions: A two-dose regimen of BNT162b2 conferred 95% protection against Covid-19 in persons 16 years of age or older. Safety over a median of 2 months was similar to that of other viral vaccines. (Funded by BioNTech and Pfizer; ClinicalTrials.gov number, NCT04368728.).<br /> (Copyright © 2020 Massachusetts Medical Society.)

Details

Language :
English
ISSN :
1533-4406
Volume :
383
Issue :
27
Database :
MEDLINE
Journal :
The New England journal of medicine
Publication Type :
Academic Journal
Accession number :
33301246
Full Text :
https://doi.org/10.1056/NEJMoa2034577