Evaluation of the safety and immunogenicity of different COVID-19 vaccine combinations in healthy individuals: study protocol for a randomized, subject-blinded, controlled phase 3 trial [PRIBIVAC]

Over 2021, COVID-19 vaccination programs worldwide focused on raising population immunity through the primary COVID-19 vaccine series. In Singapore, two mRNA vaccines (BNT162b2 and mRNA-1273) and the inactivated vaccine CoronaVac are currently authorized under the National Vaccination Programme for...

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Main Authors: Poh, Xuan Ying, Lee, I. Russel, Lim, Clarissa, Teo, Jefanie, Rao, Suma, Chia, Po Ying, Ong, Sean W. X., Lee, Tau Hong, Lin, Ray J. H., Ng, Lisa F. P., Ren, Ee Chee, Lin, Raymond T. P., Wang, Lin-Fa, Renia, Laurent, Lye, David C., Young, Barnaby Edward
Other Authors: Lee Kong Chian School of Medicine (LKCMedicine)
Format: Article
Language:English
Published: 2023
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Online Access:https://hdl.handle.net/10356/171102
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Institution: Nanyang Technological University
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spelling sg-ntu-dr.10356-1711022023-10-15T15:38:45Z Evaluation of the safety and immunogenicity of different COVID-19 vaccine combinations in healthy individuals: study protocol for a randomized, subject-blinded, controlled phase 3 trial [PRIBIVAC] Poh, Xuan Ying Lee, I. Russel Lim, Clarissa Teo, Jefanie Rao, Suma Chia, Po Ying Ong, Sean W. X. Lee, Tau Hong Lin, Ray J. H. Ng, Lisa F. P. Ren, Ee Chee Lin, Raymond T. P. Wang, Lin-Fa Renia, Laurent Lye, David C. Young, Barnaby Edward Lee Kong Chian School of Medicine (LKCMedicine) National Centre for Infectious Diseases Tan Tock Seng Hospital National University of Singapore Science::Medicine COVID-19 SARS-CoV-2 Over 2021, COVID-19 vaccination programs worldwide focused on raising population immunity through the primary COVID-19 vaccine series. In Singapore, two mRNA vaccines (BNT162b2 and mRNA-1273) and the inactivated vaccine CoronaVac are currently authorized under the National Vaccination Programme for use as the primary vaccination series. More than 90% of the Singapore population has received at least one dose of a COVID-19 vaccine as of December 2021. With the demonstration that vaccine effectiveness wanes in the months after vaccination, and the emergence of Omicron which evades host immunity from prior infection and/or vaccination, attention in many countries has shifted to how best to maintain immunity through booster vaccinations. National Medical Research Council (NMRC) Published version This study is funded by the National Medical Research Council (NMRC) COVID19 Research Fund (COVID19RF-0011, COVID19RF-0018). 2023-10-13T05:17:18Z 2023-10-13T05:17:18Z 2022 Journal Article Poh, X. Y., Lee, I. R., Lim, C., Teo, J., Rao, S., Chia, P. Y., Ong, S. W. X., Lee, T. H., Lin, R. J. H., Ng, L. F. P., Ren, E. C., Lin, R. T. P., Wang, L., Renia, L., Lye, D. C. & Young, B. E. (2022). Evaluation of the safety and immunogenicity of different COVID-19 vaccine combinations in healthy individuals: study protocol for a randomized, subject-blinded, controlled phase 3 trial [PRIBIVAC]. Trials, 23(1), 498-. https://dx.doi.org/10.1186/s13063-022-06345-2 1745-6215 https://hdl.handle.net/10356/171102 10.1186/s13063-022-06345-2 35710572 2-s2.0-85132081941 1 23 498 en COVID19RF-0011 COVID19RF-0018 Trials © 2022 The Author(s). Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativeco mmons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Medicine
COVID-19
SARS-CoV-2
spellingShingle Science::Medicine
COVID-19
SARS-CoV-2
Poh, Xuan Ying
Lee, I. Russel
Lim, Clarissa
Teo, Jefanie
Rao, Suma
Chia, Po Ying
Ong, Sean W. X.
Lee, Tau Hong
Lin, Ray J. H.
Ng, Lisa F. P.
Ren, Ee Chee
Lin, Raymond T. P.
Wang, Lin-Fa
Renia, Laurent
Lye, David C.
Young, Barnaby Edward
Evaluation of the safety and immunogenicity of different COVID-19 vaccine combinations in healthy individuals: study protocol for a randomized, subject-blinded, controlled phase 3 trial [PRIBIVAC]
description Over 2021, COVID-19 vaccination programs worldwide focused on raising population immunity through the primary COVID-19 vaccine series. In Singapore, two mRNA vaccines (BNT162b2 and mRNA-1273) and the inactivated vaccine CoronaVac are currently authorized under the National Vaccination Programme for use as the primary vaccination series. More than 90% of the Singapore population has received at least one dose of a COVID-19 vaccine as of December 2021. With the demonstration that vaccine effectiveness wanes in the months after vaccination, and the emergence of Omicron which evades host immunity from prior infection and/or vaccination, attention in many countries has shifted to how best to maintain immunity through booster vaccinations.
author2 Lee Kong Chian School of Medicine (LKCMedicine)
author_facet Lee Kong Chian School of Medicine (LKCMedicine)
Poh, Xuan Ying
Lee, I. Russel
Lim, Clarissa
Teo, Jefanie
Rao, Suma
Chia, Po Ying
Ong, Sean W. X.
Lee, Tau Hong
Lin, Ray J. H.
Ng, Lisa F. P.
Ren, Ee Chee
Lin, Raymond T. P.
Wang, Lin-Fa
Renia, Laurent
Lye, David C.
Young, Barnaby Edward
format Article
author Poh, Xuan Ying
Lee, I. Russel
Lim, Clarissa
Teo, Jefanie
Rao, Suma
Chia, Po Ying
Ong, Sean W. X.
Lee, Tau Hong
Lin, Ray J. H.
Ng, Lisa F. P.
Ren, Ee Chee
Lin, Raymond T. P.
Wang, Lin-Fa
Renia, Laurent
Lye, David C.
Young, Barnaby Edward
author_sort Poh, Xuan Ying
title Evaluation of the safety and immunogenicity of different COVID-19 vaccine combinations in healthy individuals: study protocol for a randomized, subject-blinded, controlled phase 3 trial [PRIBIVAC]
title_short Evaluation of the safety and immunogenicity of different COVID-19 vaccine combinations in healthy individuals: study protocol for a randomized, subject-blinded, controlled phase 3 trial [PRIBIVAC]
title_full Evaluation of the safety and immunogenicity of different COVID-19 vaccine combinations in healthy individuals: study protocol for a randomized, subject-blinded, controlled phase 3 trial [PRIBIVAC]
title_fullStr Evaluation of the safety and immunogenicity of different COVID-19 vaccine combinations in healthy individuals: study protocol for a randomized, subject-blinded, controlled phase 3 trial [PRIBIVAC]
title_full_unstemmed Evaluation of the safety and immunogenicity of different COVID-19 vaccine combinations in healthy individuals: study protocol for a randomized, subject-blinded, controlled phase 3 trial [PRIBIVAC]
title_sort evaluation of the safety and immunogenicity of different covid-19 vaccine combinations in healthy individuals: study protocol for a randomized, subject-blinded, controlled phase 3 trial [pribivac]
publishDate 2023
url https://hdl.handle.net/10356/171102
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