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Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine through 6 Months

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-1...

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Autores principales: Thomas, Stephen J., Moreira, Edson D., Kitchin, Nicholas, Absalon, Judith, Gurtman, Alejandra, Lockhart, Stephen, Perez, John L., Pérez Marc, Gonzalo, Polack, Fernando P., Zerbini, Cristiano, Bailey, Ruth, Swanson, Kena A., Xu, Xia, Roychoudhury, Satrajit, Koury, Kenneth, Bouguermouh, Salim, Kalina, Warren V., Cooper, David, Frenck, Robert W., Hammitt, Laura L., Türeci, Özlem, Nell, Haylene, Schaefer, Axel, Ünal, Serhat, Yang, Qi, Liberator, Paul, Tresnan, Dina B., Mather, Susan, Dormitzer, Philip R., Şahin, Uğur, Gruber, William C., Jansen, Kathrin U.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Massachusetts Medical Society 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8461570/
https://www.ncbi.nlm.nih.gov/pubmed/34525277
http://dx.doi.org/10.1056/NEJMoa2110345
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author Thomas, Stephen J.
Moreira, Edson D.
Kitchin, Nicholas
Absalon, Judith
Gurtman, Alejandra
Lockhart, Stephen
Perez, John L.
Pérez Marc, Gonzalo
Polack, Fernando P.
Zerbini, Cristiano
Bailey, Ruth
Swanson, Kena A.
Xu, Xia
Roychoudhury, Satrajit
Koury, Kenneth
Bouguermouh, Salim
Kalina, Warren V.
Cooper, David
Frenck, Robert W.
Hammitt, Laura L.
Türeci, Özlem
Nell, Haylene
Schaefer, Axel
Ünal, Serhat
Yang, Qi
Liberator, Paul
Tresnan, Dina B.
Mather, Susan
Dormitzer, Philip R.
Şahin, Uğur
Gruber, William C.
Jansen, Kathrin U.
author_facet Thomas, Stephen J.
Moreira, Edson D.
Kitchin, Nicholas
Absalon, Judith
Gurtman, Alejandra
Lockhart, Stephen
Perez, John L.
Pérez Marc, Gonzalo
Polack, Fernando P.
Zerbini, Cristiano
Bailey, Ruth
Swanson, Kena A.
Xu, Xia
Roychoudhury, Satrajit
Koury, Kenneth
Bouguermouh, Salim
Kalina, Warren V.
Cooper, David
Frenck, Robert W.
Hammitt, Laura L.
Türeci, Özlem
Nell, Haylene
Schaefer, Axel
Ünal, Serhat
Yang, Qi
Liberator, Paul
Tresnan, Dina B.
Mather, Susan
Dormitzer, Philip R.
Şahin, Uğur
Gruber, William C.
Jansen, Kathrin U.
author_sort Thomas, Stephen J.
collection PubMed
description 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.)
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spelling pubmed-84615702021-09-27 Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine through 6 Months Thomas, Stephen J. Moreira, Edson D. Kitchin, Nicholas Absalon, Judith Gurtman, Alejandra Lockhart, Stephen Perez, John L. Pérez Marc, Gonzalo Polack, Fernando P. Zerbini, Cristiano Bailey, Ruth Swanson, Kena A. Xu, Xia Roychoudhury, Satrajit Koury, Kenneth Bouguermouh, Salim Kalina, Warren V. Cooper, David Frenck, Robert W. Hammitt, Laura L. Türeci, Özlem Nell, Haylene Schaefer, Axel Ünal, Serhat Yang, Qi Liberator, Paul Tresnan, Dina B. Mather, Susan Dormitzer, Philip R. Şahin, Uğur Gruber, William C. Jansen, Kathrin U. N Engl J Med Original Article 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.) Massachusetts Medical Society 2021-09-15 /pmc/articles/PMC8461570/ /pubmed/34525277 http://dx.doi.org/10.1056/NEJMoa2110345 Text en Copyright © 2021 Massachusetts Medical Society. All rights reserved. http://www.nejmgroup.org/legal/terms-of-use.htm This article is made available via the PMC Open Access Subset for unrestricted re-use, except commercial resale, and analyses in any form or by any means with acknowledgment of the original source. PMC is granted a license to make this article available via PMC and Europe PMC, subject to existing copyright protections.
spellingShingle Original Article
Thomas, Stephen J.
Moreira, Edson D.
Kitchin, Nicholas
Absalon, Judith
Gurtman, Alejandra
Lockhart, Stephen
Perez, John L.
Pérez Marc, Gonzalo
Polack, Fernando P.
Zerbini, Cristiano
Bailey, Ruth
Swanson, Kena A.
Xu, Xia
Roychoudhury, Satrajit
Koury, Kenneth
Bouguermouh, Salim
Kalina, Warren V.
Cooper, David
Frenck, Robert W.
Hammitt, Laura L.
Türeci, Özlem
Nell, Haylene
Schaefer, Axel
Ünal, Serhat
Yang, Qi
Liberator, Paul
Tresnan, Dina B.
Mather, Susan
Dormitzer, Philip R.
Şahin, Uğur
Gruber, William C.
Jansen, Kathrin U.
Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine through 6 Months
title Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine through 6 Months
title_full Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine through 6 Months
title_fullStr Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine through 6 Months
title_full_unstemmed Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine through 6 Months
title_short Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine through 6 Months
title_sort safety and efficacy of the bnt162b2 mrna covid-19 vaccine through 6 months
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8461570/
https://www.ncbi.nlm.nih.gov/pubmed/34525277
http://dx.doi.org/10.1056/NEJMoa2110345
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