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Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine
15.443
Zitationen
29
Autoren
2020
Jahr
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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Autoren
- Fernando P. Polack
- Stephen J. Thomas
- Nicholas Kitchin
- Judith Absalon
- Alejandra Gurtman
- Stephen Lockhart
- John L. Perez
- Gonzalo Pérez Marc
- Edson Duarte Moreira
- Cristiano A. F. Zerbini
- Ruth Bailey
- Kena A. Swanson
- Satrajit Roychoudhury
- Kenneth Koury
- Ping Li
- Warren V. Kalina
- David Cooper
- Robert W. Frenck
- Laura L Hammitt
- Özlem Türeci
- Haylene Nell
- Axel Schaefer
- Serhat Ünal
- Dina B Tresnan
- Susan Mather
- Philip R. Dormitzer
- Uğur Şahin
- Kathrin U. Jansen
- William C. Gruber