Safety and Efficacy of a Third Dose of BNT162b2 Covid-19 Vaccine
Abstract
Active immunization with the BNT162b2 vaccine (Pfizer-BioNTech) has been a critical mitigation tool against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection during the coronavirus disease 2019 (Covid-19) pandemic. In light of reports of waning protection occurring 6 months after the primary two-dose vaccine series, data are needed on the safety and efficacy of offering a third (booster) dose in persons 16 years of age or older.
In this ongoing, placebo-controlled, randomized, phase 3 trial, we assigned participants who had received two 30-μg doses of the BNT162b2 vaccine at least 6 months earlier to be injected with a third dose of the BNT162b2 vaccine or with placebo. We assessed vaccine safety and efficacy against Covid-19 starting 7 days after the third dose.
Citation impact
- FWCI
- 32.36
- Percentile
- 100%
- References
- 22
Authors
32- EDEdson D. MoreiraCorresponding
Pfizer (United States)
- NKNicholas Kitchin
Pfizer (United States)
- XXXia Xu
Pfizer (United States)
- SSSamuel S. Dychter
Pfizer (United States)
- SLStephen Lockhart
Pfizer (United States)
Topics & keywords
- MEDLINE
- Clinical trial
- Vaccine efficacy
- Vaccination
- Patient compliance