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bivalent pfizer bnt vaccine  (Pfizer Inc)

 
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    Pfizer Inc bivalent pfizer bnt vaccine
    Bivalent Pfizer Bnt Vaccine, supplied by Pfizer Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/bivalent+pfizer+bnt+vaccine/bivalent+bnt+pfizer+vaccine/pmc12390948__mmc5-912-44-45
    Average 86 stars, based on 1 article reviews
    bivalent pfizer bnt vaccine - by Bioz Stars, 2026-10
    86/100 stars

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    Immunopeptidomics:

    Article Title: Immunogenicity and safety of ‘Comvigen’, a bivalent SARS-CoV-2 vaccine, in comparison to Comirnaty bivalent vaccine in Thailand: a phase 2, non-inferiority randomised trial
    Article Snippet: .. Sample size calculation for primary immunogenicity objective The sample size calculation is based on these hypothesis testings of immunobridging analysis determined by the results of pseudovirus neutralizing antibody titer (pSVNT-50) against wildtype virus at 4 weeks after the booster dose of COMVIGEN vaccine or BIVALENT Pfizer/BNT vaccine, including: 1) Non-inferiority is declared if the lower bound of the 95% two-sided confidence interval for GMR greater than 0.67. .. The sample size was calculated based on the assumptions that point estimate of the GMR at 0.90, non-inferiority margin of GMR at 0.67, standard deviation in natural log scale at 0.89 (according to phase 2 study comparing between ChulaCov and Pfizer vaccines).

    Article Title: Immunogenicity and safety of ‘Comvigen’, a bivalent SARS-CoV-2 vaccine, in comparison to Comirnaty bivalent vaccine in Thailand: a phase 2, non-inferiority randomised trial
    Article Snippet: .. 8.1 Sample Size Calculation Sample size calculation for primary immunogenicity objective: Version 1.0; 17SEP2024 CONFIDENTIAL Page 62 of 231 The sample size calculation is based on these hypothesis testings of immunobridging analysis determined by the results of pseudovirus neutralizing antibody titer (pSVNT-50) against wild-type virus at 4 weeks after the booster dose of COMVIGEN vaccine or BIVALENT Pfizer/BNT vaccine, including: 1) Non-inferiority is declared if the lower bound of the 95% two-sided confidence interval for GMR greater than 0.67. .. The sample size was calculated based on the assumptions that point estimate of the GMR at 0.90, non-inferiority margin of GMR at 0.67, standard deviation in natural log scale at 0.89 (according to phase 2 study comparing between ChulaCov and Pfizer vaccines).

    Virus:

    Article Title: Immunogenicity and safety of ‘Comvigen’, a bivalent SARS-CoV-2 vaccine, in comparison to Comirnaty bivalent vaccine in Thailand: a phase 2, non-inferiority randomised trial
    Article Snippet: .. Sample size calculation for primary immunogenicity objective The sample size calculation is based on these hypothesis testings of immunobridging analysis determined by the results of pseudovirus neutralizing antibody titer (pSVNT-50) against wildtype virus at 4 weeks after the booster dose of COMVIGEN vaccine or BIVALENT Pfizer/BNT vaccine, including: 1) Non-inferiority is declared if the lower bound of the 95% two-sided confidence interval for GMR greater than 0.67. .. The sample size was calculated based on the assumptions that point estimate of the GMR at 0.90, non-inferiority margin of GMR at 0.67, standard deviation in natural log scale at 0.89 (according to phase 2 study comparing between ChulaCov and Pfizer vaccines).

    Article Title: Immunogenicity and safety of ‘Comvigen’, a bivalent SARS-CoV-2 vaccine, in comparison to Comirnaty bivalent vaccine in Thailand: a phase 2, non-inferiority randomised trial
    Article Snippet: .. 8.1 Sample Size Calculation Sample size calculation for primary immunogenicity objective: Version 1.0; 17SEP2024 CONFIDENTIAL Page 62 of 231 The sample size calculation is based on these hypothesis testings of immunobridging analysis determined by the results of pseudovirus neutralizing antibody titer (pSVNT-50) against wild-type virus at 4 weeks after the booster dose of COMVIGEN vaccine or BIVALENT Pfizer/BNT vaccine, including: 1) Non-inferiority is declared if the lower bound of the 95% two-sided confidence interval for GMR greater than 0.67. .. The sample size was calculated based on the assumptions that point estimate of the GMR at 0.90, non-inferiority margin of GMR at 0.67, standard deviation in natural log scale at 0.89 (according to phase 2 study comparing between ChulaCov and Pfizer vaccines).



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