Trial reportFrontiers in immunology2026
A phase III clinical trial on the immunogenicity of a tetanus vaccine, adsorbed in individuals aged 18 years and above in China.
Trial report in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06120751 (A Clinical Trial to Evaluate the Safety and Immunogenicity of a Single Dose of Adsorbed Tetanus Vaccine in a Population Aged 18 Years and Over), which is not on this map. Not yet cited in PubMed.
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The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
A Clinical Trial to Evaluate the Safety and Immunogenicity of a Single Dose of Adsorbed Tetanus Vaccine in a Population Aged 18 Years and Over
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
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Authors and funding
18 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Objective: To evaluate the immunogenicity of a tetanus vaccine, adsorbed (TTVA) in people aged 18 years and above. Methods: A randomized, double-blinded, and positive controlled clinical trial was conducted in Bijie, Guizhou Province, China. Participants aged 18 years and above were recruited and randomly assigned 1:1 to receive the experimental (TTVA) or control tetanus vaccine, adsorbed (TT) vaccine. Serum samples were collected from all participants before vaccination, 30 days after vaccination, and 6 months after vaccination in the first 240 participants to detect tetanus toxoid IgG antibody levels. Results: At 30 days after vaccination, the geometric mean concentration (GMC) of antibodies in the experimental group and the control group were 3.205 and 2.387 ( Conclusion: TTVA vaccine has good immunogenicity in people aged 18 years and above. Clinical trial registration: https://clinicaltrials.gov, identifier NCT06120751.
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