Back to Search
Start Over
The safety, immunogenicity, and efficacy of heterologous boosting with a SARS-CoV-2 mRNA vaccine (SYS6006) in Chinese participants aged 18 years or more: a randomized, open-label, active-controlled phase 3 trial.
- Source :
-
Emerging microbes & infections [Emerg Microbes Infect] 2024 Dec; Vol. 13 (1), pp. 2320913. Date of Electronic Publication: 2024 Feb 29. - Publication Year :
- 2024
-
Abstract
- Continuous emergence of new variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), enhanced transmissibility, significant immune escape, and waning immunity call for booster vaccination. We evaluated the safety, immunogenicity, and efficacy of heterologous booster with a SARS-CoV-2 mRNA vaccine SYS6006 versus an active control vaccine in a randomized, open-label, active-controlled phase 3 trial in healthy adults aged 18 years or more who had received two or three doses of SARS-CoV-2 inactivated vaccine in China. The trial started in December 2022 and lasted for 6 months. The participants were randomized (overall ratio: 3:1) to receive one dose of SYS6006 ( N = 2999) or an ancestral receptor binding region-based, alum-adjuvanted recombinant protein SARS-CoV-2 vaccine ( N = 1000), including 520 participants in an immunogenicity subgroup. SYS6006 boosting showed good safety profiles with most AEs being grade 1 or 2, and induced robust wild-type and Omicron BA.5 neutralizing antibody response on Days 14 and 28, demonstrating immunogenicity superiority versus the control vaccine and meeting the primary objective. The relative vaccine efficacy against COVID-19 of any severity was 51.6% (95% CI, 35.5-63.7) for any variant, 66.8% (48.6-78.5) for BA.5, and 37.7% (2.4-60.3) for XBB, from Day 7 through Month 6. In the vaccinated and infected hybrid immune participants, the relative vaccine efficacy was 68.4% (31.1-85.5) against COVID-19 of any severity caused by a second infection. All COVID-19 cases were mild. SYS6006 heterologous boosting demonstrated good safety, superior immunogenicity and high efficacy against BA.5-associated COVID-19, and protected against XBB-associated COVID-19, particularly in the hybrid immune population. Trial registration: Chinese Clinical Trial Registry: ChiCTR2200066941.
- Subjects :
- Humans
Adult
Female
Male
China
Middle Aged
Young Adult
Vaccines, Synthetic immunology
Vaccines, Synthetic administration & dosage
Vaccines, Synthetic adverse effects
Adolescent
Vaccine Efficacy
Vaccines, Inactivated immunology
Vaccines, Inactivated administration & dosage
Vaccines, Inactivated adverse effects
East Asian People
COVID-19 Vaccines immunology
COVID-19 Vaccines administration & dosage
COVID-19 Vaccines adverse effects
COVID-19 prevention & control
COVID-19 immunology
COVID-19 virology
SARS-CoV-2 immunology
SARS-CoV-2 genetics
Immunization, Secondary
Antibodies, Viral blood
Antibodies, Viral immunology
Immunogenicity, Vaccine
Antibodies, Neutralizing blood
Antibodies, Neutralizing immunology
mRNA Vaccines
Subjects
Details
- Language :
- English
- ISSN :
- 2222-1751
- Volume :
- 13
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Emerging microbes & infections
- Publication Type :
- Academic Journal
- Accession number :
- 38860446
- Full Text :
- https://doi.org/10.1080/22221751.2024.2320913