Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine

Fernando P. Polack(SUNY Upstate Medical University), Stephen J. Thomas(Johns Hopkins University), Nicholas Kitchin(Institut de Recherche Vaccinale), Judith Absalon(Johns Hopkins University), Alejandra Gurtman(Institut de Recherche Vaccinale), Stephen Lockhart(Institut de Recherche Vaccinale), John L. Perez(Johns Hopkins University), Gonzalo Pérez Marc(SUNY Upstate Medical University), Edson Duarte Moreira(SUNY Upstate Medical University), Cristiano A. F. Zerbini(Institut de Recherche Vaccinale), Ruth Bailey(Johns Hopkins University), Kena A. Swanson(Johns Hopkins University), Satrajit Roychoudhury(SUNY Upstate Medical University), Kenneth Koury(SUNY Upstate Medical University), Ping Li(SUNY Upstate Medical University), Warren V. Kalina(SUNY Upstate Medical University), David Cooper(SUNY Upstate Medical University), Robert W. Frenck(Institut de Recherche Vaccinale), Laura L Hammitt(Johns Hopkins University), Özlem Türeci(Institut de Recherche Vaccinale), Haylene Nell(Johns Hopkins University), Axel Schaefer(SUNY Upstate Medical University), Serhat Ünal(Institut de Recherche Vaccinale), Dina B Tresnan(Institut de Recherche Vaccinale), Susan Mather(Institut de Recherche Vaccinale), Philip R. Dormitzer(Johns Hopkins University), Uğur Şahin(SUNY Upstate Medical University), Kathrin U. Jansen(SUNY Upstate Medical University), William C. Gruber(SUNY Upstate Medical University)
New England Journal of Medicine
December 10, 2020
Cited by 15,454Open Access
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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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