New England Journal of Medicine, volume 383, issue 27, pages 2603-2615
Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine
Fernando P. Polack
1
,
Stephen H. Thomas
1
,
Nicholas Kitchin
1
,
Judith Absalon
1
,
A C Gurtman
1
,
John L. Perez
1
,
Gonzalo Pérez Marc
1
,
Edson DS. Moreira
1
,
Cristiano A.F. Zerbini
1
,
RUTH BAILEY
1
,
Kena A. Swanson
1
,
Satrajit Roychoudhury
1
,
Kenneth Koury
1
,
Ping Li
1
,
Warren V. Kalina
1
,
David R. Cooper
1
,
Robert W. Frenck
1
,
Laura L. Hammitt
1
,
Özlem Türeci
1
,
Haylene Nell
1
,
Axel Schaefer
1
,
Serhat Unal
1
,
Dina B. Tresnan
1
,
Susan Mather
1
,
Philip R. Dormitzer
1
,
Ugur Sahin
1
,
Kathrin U. Jansen
1
,
WILLIAM C. GRUBER
1
1
From Fundacion INFANT (F.P.P.) and iTrials-Hospital Militar Central (G.P.M.), Buenos Aires; State University of New York, Upstate Medical University, Syracuse (S.J.T.), and Vaccine Research and Development, Pfizer, Pearl River (J.A., A.G., K.A.S., K.K., W.V.K., D.C., P.R.D., K.U.J., W.C.G.) — both in New York; Vaccine Research and Development, Pfizer, Hurley, United Kingdom (N.K., S.L., R.B.); Vaccine Research and Development (J.L.P., P.L.) and Worldwide Safety, Safety Surveillance and Risk Management (S...
Publication type: Journal Article
Publication date: 2020-12-10
Journal:
New England Journal of Medicine
scimago Q1
SJR: 20.544
CiteScore: 145.4
Impact factor: 96.2
ISSN: 00284793, 15334406
PubMed ID:
33301246
General Medicine
Abstract
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. 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. 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. 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.)
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