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2363. Three-Month Safety and Immunogenicity of Bivalent SARS-CoV-2 Omicron-Containing Booster Vaccines: Interim Results From a Phase 3, Randomized, Observer-Blind, Active-Controlled Trial

BACKGROUND: Updated COVID-19 vaccines have been developed to help broaden protection against circulating SARS-CoV-2 variants. Here we present a 3-month interim analysis from a phase 3, randomized, observer-blind, active-controlled study of 2 omicron BA.1-containing vaccines: BA.1-monovalent mRNA-127...

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Autores principales: Lee, Ivan T, Cosgrove, Catherine A, Moore, Patrick, Bula, Marcin, Kalra, Philip, Dargan, Paul, Clark, Rebecca, Boffito, Marta, Sheridan, Ray, Bethune, Claire, Burns, Fiona, Saralaya, Dinesh, Nally, Rhiannon, Duncan, Christopher J A, Chadwick, David, Palfreeman, Adrian, Ramos, Alberto San Francisco, Heath, Paul T, Girard, Bethany, Sellers, Kristen, de Windt, Elizabeth, Sutherland, Andrea, Tracy, LaRee, Zhou, Honghong, Miller, Jacqueline, Priddy, Frances, Chalkias, Spyros, Das, Rituparna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677689/
http://dx.doi.org/10.1093/ofid/ofad500.1984
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author Lee, Ivan T
Cosgrove, Catherine A
Moore, Patrick
Bula, Marcin
Kalra, Philip
Dargan, Paul
Clark, Rebecca
Boffito, Marta
Sheridan, Ray
Bethune, Claire
Burns, Fiona
Saralaya, Dinesh
Nally, Rhiannon
Duncan, Christopher J A
Chadwick, David
Palfreeman, Adrian
Ramos, Alberto San Francisco
Heath, Paul T
Girard, Bethany
Sellers, Kristen
de Windt, Elizabeth
Sutherland, Andrea
Tracy, LaRee
Zhou, Honghong
Miller, Jacqueline
Priddy, Frances
Chalkias, Spyros
Das, Rituparna
author_facet Lee, Ivan T
Cosgrove, Catherine A
Moore, Patrick
Bula, Marcin
Kalra, Philip
Dargan, Paul
Clark, Rebecca
Boffito, Marta
Sheridan, Ray
Bethune, Claire
Burns, Fiona
Saralaya, Dinesh
Nally, Rhiannon
Duncan, Christopher J A
Chadwick, David
Palfreeman, Adrian
Ramos, Alberto San Francisco
Heath, Paul T
Girard, Bethany
Sellers, Kristen
de Windt, Elizabeth
Sutherland, Andrea
Tracy, LaRee
Zhou, Honghong
Miller, Jacqueline
Priddy, Frances
Chalkias, Spyros
Das, Rituparna
author_sort Lee, Ivan T
collection PubMed
description BACKGROUND: Updated COVID-19 vaccines have been developed to help broaden protection against circulating SARS-CoV-2 variants. Here we present a 3-month interim analysis from a phase 3, randomized, observer-blind, active-controlled study of 2 omicron BA.1-containing vaccines: BA.1-monovalent mRNA-1273.529 (BA.1 variant only) and BA.1-bivalent mRNA-1273.214 (SARS-CoV-2 Wuhan-Hu-1 strain and BA.1 variant). METHODS: This multicenter study evaluated safety and immunogenicity of the BA.1-monovalent (Part 1) and -bivalent (Part 2) vaccines in individuals aged ≥ 16 years in the United Kingdom (NCT05249829). Eligible participants previously received 2 or 3 doses of an authorized/approved COVID-19 vaccine and were randomly assigned 1:1 to receive a 50-µg booster of the original mRNA-1273 vaccine or either BA.1-monovalent or -bivalent vaccines. Safety and reactogenicity up to 3 months post-booster were evaluated. Immunogenicity objectives were to demonstrate non-inferiority and/or superiority of BA.1-monovalent or -bivalent vaccine-elicited immune responses to BA.1 and the ancestral strain (D614G) at Day 29 and Month 3 compared with a booster dose of mRNA-1273 in participants without evidence of baseline SARS-CoV-2 infection up to day of analysis visit on Day 29 or Month 3. RESULTS: At the interim analysis, 724 (Part 1) and 2824 (Part 2) booster recipients were included in the safety analysis set. BA.1-monovalent and -bivalent booster vaccines were well-tolerated with no new safety concerns identified. Compared with mRNA-1273, a fourth dose of BA.1-monovalent or -bivalent vaccine elicited superior nAb responses against omicron BA.1 at Month 3, with geometric mean ratios (GMRs) of 1.77 (96% CI, 1.55-2.02) and 1.67 (96% CI, 1.54-1.81), respectively. Non-inferior (lower bound of confidence interval ≥ 0.67) nAb responses against D614G were also demonstrated with GMRs of 0.80 (95% CI, 0.71-0.90) for BA.1-monovalent and 1.11 (96% CI, 1.03-1.18) for -bivalent vaccines. CONCLUSION: The BA.1 monovalent and bivalent booster vaccines elicited nAb responses against BA.1 that remain superior to mRNA-1273 at 3 months post-booster with no new safety concerns. These results support variant-updated vaccines to protect against evolving SARS-CoV-2. DISCLOSURES: Ivan T. Lee, MD, PhD, Moderna, Inc.: Salary|Moderna, Inc.: Stocks/Bonds Catherine A. Cosgrove, PhD, Novavax: Advisor/Consultant|Novavax: Grant/Research Support|Novavax: Speaker Patrick Moore, MRCGP, AstraZeneca: Advisor/Consultant|AstraZeneca: Grant/Research Support|GSK: Advisor/Consultant|GSK: Grant/Research Support|Janssen: Advisor/Consultant|Janssen: Grant/Research Support|Medicago: Advisor/Consultant|Medicago: Grant/Research Support|Moderna, Inc.: Advisor/Consultant|Moderna, Inc.: Grant/Research Support|MSD: Advisor/Consultant|MSD: Grant/Research Support|Novavax: Advisor/Consultant|Novavax: Grant/Research Support|Sanofi: Advisor/Consultant|Sanofi: Grant/Research Support Philip Kalra, MD, Astellas: Advisor/Consultant|Astellas: Grant/Research Support|AstraZeneca: Advisor/Consultant|AstraZeneca: Grant/Research Support|Bayer: Advisor/Consultant|Bayer: Grant/Research Support|Evotec: Advisor/Consultant|Evotec: Grant/Research Support|Fresenius: Advisor/Consultant|Fresenius: Grant/Research Support|GSK: Advisor/Consultant|GSK: Grant/Research Support|Lilly: Advisor/Consultant|Lilly: Grant/Research Support|Otsuka: Advisor/Consultant|Otsuka: Grant/Research Support|Pfizer: Advisor/Consultant|Pfizer: Grant/Research Support|Pharmacosmos: Advisor/Consultant|Pharmacosmos: Grant/Research Support|Unicyte: Advisor/Consultant|Unicyte: Grant/Research Support|Vifor: Advisor/Consultant|Vifor: Grant/Research Support Paul Dargan, MBBS, Moderna, Inc.: Grant/Research Support Marta Boffito, MD, PhD, FRCP, AstraZeneca: Honoraria|ATEA: Advisor/Consultant|ATEA: Honoraria|Gilead: Advisor/Consultant|Gilead: Grant/Research Support|Gilead: Honoraria|GSK: Advisor/Consultant|GSK: Grant/Research Support|Moderna: Grant/Research Support|MSD: Advisor/Consultant|MSD: Grant/Research Support|MSD: Honoraria|Novavax: Grant/Research Support|Pfizer: Advisor/Consultant|Pfizer: Grant/Research Support|Roche: Advisor/Consultant|Roche: Grant/Research Support|Valneva: Grant/Research Support|ViiV: Advisor/Consultant|ViiV: Grant/Research Support Fiona Burns, PhD, Gilead Sciences Ltd.: Grant/Research Support|Gilead Sciences Ltd.: Speaker Fees Christopher J. A. Duncan, DPhil, MRC: Grant/Research Support|Wellcome Trust: Grant/Research Support David Chadwick, PhD, Gilead Sciences Ltd: Grant/Research Support|GSK: Grant/Research Support|Janssen: Grant/Research Support|Moderna, Inc.: Grant/Research Support|Novavax: Grant/Research Support|ViiV Healthcare: Grant/Research Support Adrian Palfreeman, MBBS, University Hospital of Leicester NHS Trust. - Leicester (United Kingdom): Employee Paul T. Heath, FRCPCH, AstraZeneca: Grant/Research Support|Janssen: Grant/Research Support|Moderna, Inc.: Grant/Research Support|Novavax: Grant/Research Support|Pfizer: Grant/Research Support|Valneva: Grant/Research Support Bethany Girard, Ph.D., Moderna, Inc.: salary|Moderna, Inc.: Stocks/Bonds Kristen Sellers, PhD, Moderna, Inc.: Salary|Moderna, Inc.: Stocks/Bonds Elizabeth de Windt, MPH, Moderna, Inc.: Salary|Moderna, Inc.: Stocks/Bonds Andrea Sutherland, M.D., MPH, Moderna, Inc.: Salary|Moderna, Inc.: Stocks/Bonds LaRee Tracy, PhD, Moderna, Inc.: Salary|Moderna, Inc.: Stocks/Bonds Honghong Zhou, Ph.D., Moderna, Inc.: salary|Moderna, Inc.: Stocks/Bonds Jacqueline Miller, MD, Moderna, Inc.: salary|Moderna, Inc.: Stocks/Bonds Frances Priddy, MD, MPH, Moderna, Inc.: Salary|Moderna, Inc.: Stocks/Bonds Spyros Chalkias, MD, Moderna, Inc.: Salary|Moderna, Inc.: Stocks/Bonds Rituparna Das, M.D., Moderna, Inc.: Salary|Moderna, Inc.: Stocks/Bonds
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spelling pubmed-106776892023-11-27 2363. Three-Month Safety and Immunogenicity of Bivalent SARS-CoV-2 Omicron-Containing Booster Vaccines: Interim Results From a Phase 3, Randomized, Observer-Blind, Active-Controlled Trial Lee, Ivan T Cosgrove, Catherine A Moore, Patrick Bula, Marcin Kalra, Philip Dargan, Paul Clark, Rebecca Boffito, Marta Sheridan, Ray Bethune, Claire Burns, Fiona Saralaya, Dinesh Nally, Rhiannon Duncan, Christopher J A Chadwick, David Palfreeman, Adrian Ramos, Alberto San Francisco Heath, Paul T Girard, Bethany Sellers, Kristen de Windt, Elizabeth Sutherland, Andrea Tracy, LaRee Zhou, Honghong Miller, Jacqueline Priddy, Frances Chalkias, Spyros Das, Rituparna Open Forum Infect Dis Abstract BACKGROUND: Updated COVID-19 vaccines have been developed to help broaden protection against circulating SARS-CoV-2 variants. Here we present a 3-month interim analysis from a phase 3, randomized, observer-blind, active-controlled study of 2 omicron BA.1-containing vaccines: BA.1-monovalent mRNA-1273.529 (BA.1 variant only) and BA.1-bivalent mRNA-1273.214 (SARS-CoV-2 Wuhan-Hu-1 strain and BA.1 variant). METHODS: This multicenter study evaluated safety and immunogenicity of the BA.1-monovalent (Part 1) and -bivalent (Part 2) vaccines in individuals aged ≥ 16 years in the United Kingdom (NCT05249829). Eligible participants previously received 2 or 3 doses of an authorized/approved COVID-19 vaccine and were randomly assigned 1:1 to receive a 50-µg booster of the original mRNA-1273 vaccine or either BA.1-monovalent or -bivalent vaccines. Safety and reactogenicity up to 3 months post-booster were evaluated. Immunogenicity objectives were to demonstrate non-inferiority and/or superiority of BA.1-monovalent or -bivalent vaccine-elicited immune responses to BA.1 and the ancestral strain (D614G) at Day 29 and Month 3 compared with a booster dose of mRNA-1273 in participants without evidence of baseline SARS-CoV-2 infection up to day of analysis visit on Day 29 or Month 3. RESULTS: At the interim analysis, 724 (Part 1) and 2824 (Part 2) booster recipients were included in the safety analysis set. BA.1-monovalent and -bivalent booster vaccines were well-tolerated with no new safety concerns identified. Compared with mRNA-1273, a fourth dose of BA.1-monovalent or -bivalent vaccine elicited superior nAb responses against omicron BA.1 at Month 3, with geometric mean ratios (GMRs) of 1.77 (96% CI, 1.55-2.02) and 1.67 (96% CI, 1.54-1.81), respectively. Non-inferior (lower bound of confidence interval ≥ 0.67) nAb responses against D614G were also demonstrated with GMRs of 0.80 (95% CI, 0.71-0.90) for BA.1-monovalent and 1.11 (96% CI, 1.03-1.18) for -bivalent vaccines. CONCLUSION: The BA.1 monovalent and bivalent booster vaccines elicited nAb responses against BA.1 that remain superior to mRNA-1273 at 3 months post-booster with no new safety concerns. These results support variant-updated vaccines to protect against evolving SARS-CoV-2. DISCLOSURES: Ivan T. Lee, MD, PhD, Moderna, Inc.: Salary|Moderna, Inc.: Stocks/Bonds Catherine A. Cosgrove, PhD, Novavax: Advisor/Consultant|Novavax: Grant/Research Support|Novavax: Speaker Patrick Moore, MRCGP, AstraZeneca: Advisor/Consultant|AstraZeneca: Grant/Research Support|GSK: Advisor/Consultant|GSK: Grant/Research Support|Janssen: Advisor/Consultant|Janssen: Grant/Research Support|Medicago: Advisor/Consultant|Medicago: Grant/Research Support|Moderna, Inc.: Advisor/Consultant|Moderna, Inc.: Grant/Research Support|MSD: Advisor/Consultant|MSD: Grant/Research Support|Novavax: Advisor/Consultant|Novavax: Grant/Research Support|Sanofi: Advisor/Consultant|Sanofi: Grant/Research Support Philip Kalra, MD, Astellas: Advisor/Consultant|Astellas: Grant/Research Support|AstraZeneca: Advisor/Consultant|AstraZeneca: Grant/Research Support|Bayer: Advisor/Consultant|Bayer: Grant/Research Support|Evotec: Advisor/Consultant|Evotec: Grant/Research Support|Fresenius: Advisor/Consultant|Fresenius: Grant/Research Support|GSK: Advisor/Consultant|GSK: Grant/Research Support|Lilly: Advisor/Consultant|Lilly: Grant/Research Support|Otsuka: Advisor/Consultant|Otsuka: Grant/Research Support|Pfizer: Advisor/Consultant|Pfizer: Grant/Research Support|Pharmacosmos: Advisor/Consultant|Pharmacosmos: Grant/Research Support|Unicyte: Advisor/Consultant|Unicyte: Grant/Research Support|Vifor: Advisor/Consultant|Vifor: Grant/Research Support Paul Dargan, MBBS, Moderna, Inc.: Grant/Research Support Marta Boffito, MD, PhD, FRCP, AstraZeneca: Honoraria|ATEA: Advisor/Consultant|ATEA: Honoraria|Gilead: Advisor/Consultant|Gilead: Grant/Research Support|Gilead: Honoraria|GSK: Advisor/Consultant|GSK: Grant/Research Support|Moderna: Grant/Research Support|MSD: Advisor/Consultant|MSD: Grant/Research Support|MSD: Honoraria|Novavax: Grant/Research Support|Pfizer: Advisor/Consultant|Pfizer: Grant/Research Support|Roche: Advisor/Consultant|Roche: Grant/Research Support|Valneva: Grant/Research Support|ViiV: Advisor/Consultant|ViiV: Grant/Research Support Fiona Burns, PhD, Gilead Sciences Ltd.: Grant/Research Support|Gilead Sciences Ltd.: Speaker Fees Christopher J. A. Duncan, DPhil, MRC: Grant/Research Support|Wellcome Trust: Grant/Research Support David Chadwick, PhD, Gilead Sciences Ltd: Grant/Research Support|GSK: Grant/Research Support|Janssen: Grant/Research Support|Moderna, Inc.: Grant/Research Support|Novavax: Grant/Research Support|ViiV Healthcare: Grant/Research Support Adrian Palfreeman, MBBS, University Hospital of Leicester NHS Trust. - Leicester (United Kingdom): Employee Paul T. Heath, FRCPCH, AstraZeneca: Grant/Research Support|Janssen: Grant/Research Support|Moderna, Inc.: Grant/Research Support|Novavax: Grant/Research Support|Pfizer: Grant/Research Support|Valneva: Grant/Research Support Bethany Girard, Ph.D., Moderna, Inc.: salary|Moderna, Inc.: Stocks/Bonds Kristen Sellers, PhD, Moderna, Inc.: Salary|Moderna, Inc.: Stocks/Bonds Elizabeth de Windt, MPH, Moderna, Inc.: Salary|Moderna, Inc.: Stocks/Bonds Andrea Sutherland, M.D., MPH, Moderna, Inc.: Salary|Moderna, Inc.: Stocks/Bonds LaRee Tracy, PhD, Moderna, Inc.: Salary|Moderna, Inc.: Stocks/Bonds Honghong Zhou, Ph.D., Moderna, Inc.: salary|Moderna, Inc.: Stocks/Bonds Jacqueline Miller, MD, Moderna, Inc.: salary|Moderna, Inc.: Stocks/Bonds Frances Priddy, MD, MPH, Moderna, Inc.: Salary|Moderna, Inc.: Stocks/Bonds Spyros Chalkias, MD, Moderna, Inc.: Salary|Moderna, Inc.: Stocks/Bonds Rituparna Das, M.D., Moderna, Inc.: Salary|Moderna, Inc.: Stocks/Bonds Oxford University Press 2023-11-27 /pmc/articles/PMC10677689/ http://dx.doi.org/10.1093/ofid/ofad500.1984 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Lee, Ivan T
Cosgrove, Catherine A
Moore, Patrick
Bula, Marcin
Kalra, Philip
Dargan, Paul
Clark, Rebecca
Boffito, Marta
Sheridan, Ray
Bethune, Claire
Burns, Fiona
Saralaya, Dinesh
Nally, Rhiannon
Duncan, Christopher J A
Chadwick, David
Palfreeman, Adrian
Ramos, Alberto San Francisco
Heath, Paul T
Girard, Bethany
Sellers, Kristen
de Windt, Elizabeth
Sutherland, Andrea
Tracy, LaRee
Zhou, Honghong
Miller, Jacqueline
Priddy, Frances
Chalkias, Spyros
Das, Rituparna
2363. Three-Month Safety and Immunogenicity of Bivalent SARS-CoV-2 Omicron-Containing Booster Vaccines: Interim Results From a Phase 3, Randomized, Observer-Blind, Active-Controlled Trial
title 2363. Three-Month Safety and Immunogenicity of Bivalent SARS-CoV-2 Omicron-Containing Booster Vaccines: Interim Results From a Phase 3, Randomized, Observer-Blind, Active-Controlled Trial
title_full 2363. Three-Month Safety and Immunogenicity of Bivalent SARS-CoV-2 Omicron-Containing Booster Vaccines: Interim Results From a Phase 3, Randomized, Observer-Blind, Active-Controlled Trial
title_fullStr 2363. Three-Month Safety and Immunogenicity of Bivalent SARS-CoV-2 Omicron-Containing Booster Vaccines: Interim Results From a Phase 3, Randomized, Observer-Blind, Active-Controlled Trial
title_full_unstemmed 2363. Three-Month Safety and Immunogenicity of Bivalent SARS-CoV-2 Omicron-Containing Booster Vaccines: Interim Results From a Phase 3, Randomized, Observer-Blind, Active-Controlled Trial
title_short 2363. Three-Month Safety and Immunogenicity of Bivalent SARS-CoV-2 Omicron-Containing Booster Vaccines: Interim Results From a Phase 3, Randomized, Observer-Blind, Active-Controlled Trial
title_sort 2363. three-month safety and immunogenicity of bivalent sars-cov-2 omicron-containing booster vaccines: interim results from a phase 3, randomized, observer-blind, active-controlled trial
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677689/
http://dx.doi.org/10.1093/ofid/ofad500.1984
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