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Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine through 6 Months
- Source :
- The New England Journal of Medicine
- Publication Year :
- 2021
- Publisher :
- Massachusetts Medical Society, 2021.
-
Abstract
- Background BNT162b2 is a lipid nanoparticle–formulated, nucleoside-modified RNA vaccine encoding a prefusion-stabilized, membrane-anchored severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) full-length spike protein. BNT162b2 is highly efficacious against coronavirus disease 2019 (Covid-19) and is currently approved, conditionally approved, or authorized for emergency use worldwide. At the time of initial authorization, data beyond 2 months after vaccination were unavailable. Methods In an ongoing, placebo-controlled, observer-blinded, multinational, pivotal efficacy trial, we randomly assigned 44,165 participants 16 years of age or older and 2264 participants 12 to 15 years of age to receive two 30-μg doses, at 21 days apart, of BNT162b2 or placebo. The trial end points were vaccine efficacy against laboratory-confirmed Covid-19 and safety, which were both evaluated through 6 months after vaccination. Results BNT162b2 continued to be safe and have an acceptable adverse-event profile. Few participants had adverse events leading to withdrawal from the trial. Vaccine efficacy against Covid-19 was 91.3% (95% confidence interval [CI], 89.0 to 93.2) through 6 months of follow-up among the participants without evidence of previous SARS-CoV-2 infection who could be evaluated. There was a gradual decline in vaccine efficacy. Vaccine efficacy of 86 to 100% was seen across countries and in populations with diverse ages, sexes, race or ethnic groups, and risk factors for Covid-19 among participants without evidence of previous infection with SARS-CoV-2. Vaccine efficacy against severe disease was 96.7% (95% CI, 80.3 to 99.9). In South Africa, where the SARS-CoV-2 variant of concern B.1.351 (or beta) was predominant, a vaccine efficacy of 100% (95% CI, 53.5 to 100) was observed. Conclusions Through 6 months of follow-up and despite a gradual decline in vaccine efficacy, BNT162b2 had a favorable safety profile and was highly efficacious in preventing Covid-19. (Funded by BioNTech and Pfizer; ClinicalTrials.gov number, NCT04368728.)
- Subjects :
- Adult
Male
medicine.medical_specialty
COVID-19 Vaccines
Adolescent
Coronavirus disease 2019 (COVID-19)
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)
Immunization, Secondary
Antibodies, Viral
Placebo
Young Adult
Immunogenicity, Vaccine
Internal medicine
Humans
Medicine
Single-Blind Method
Child
Adverse effect
BNT162 Vaccine
Aged
Aged, 80 and over
SARS-CoV-2
business.industry
Incidence
COVID-19
General Medicine
Middle Aged
Vaccine efficacy
Confidence interval
Vaccination
Safety profile
Treatment Outcome
Female
Original Article
business
Follow-Up Studies
Subjects
Details
- ISSN :
- 15334406 and 00284793
- Volume :
- 385
- Database :
- OpenAIRE
- Journal :
- New England Journal of Medicine
- Accession number :
- edsair.doi.dedup.....aab5607b188661fc23df4ea70c83b696