- 
             Something wrong with this record ?
 
A phase 3 study to assess the immunogenicity, safety, and tolerability of MenB-FHbp administered as a 2-dose schedule in adolescents and young adults
D. Drazan, H. Czajka, JD. Maguire, JL. Pregaldien, R. Maansson, R. O'Neill, AS. Anderson, P. Balmer, J. Beeslaar, JL. Perez
Language English Country Netherlands
Document type Clinical Trial, Phase III, Journal Article, Research Support, Non-U.S. Gov't
 NLK 
   
      ProQuest Central
   
    from 2002-01-01 to 2 months ago
   
      Nursing & Allied Health Database (ProQuest)
   
    from 2002-01-01 to 2 months ago
   
      Health & Medicine (ProQuest)
   
    from 2002-01-01 to 2 months ago
   
      Family Health Database (ProQuest)
   
    from 2002-01-01 to 2 months ago
   
      Health Management Database (ProQuest)
   
    from 2002-01-01 to 2 months ago
   
      Public Health Database (ProQuest)
   
    from 2002-01-01 to 2 months ago
    
- MeSH
- Humans MeSH
- Meningococcal Infections * prevention & control MeSH
- Meningococcal Vaccines * adverse effects MeSH
- Adolescent MeSH
- Young Adult MeSH
- Neisseria meningitidis, Serogroup B * MeSH
- Neisseria meningitidis * MeSH
- Antibodies, Bacterial MeSH
- Serogroup MeSH
- Vaccination MeSH
- Check Tag
- Humans MeSH
- Adolescent MeSH
- Young Adult MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial, Phase III MeSH
- Research Support, Non-U.S. Gov't MeSH
BACKGROUND: The MenB-FHbp vaccine is licensed to prevent meningococcal serogroup B disease on either a 2-dose (0, 6 months) or 3-dose (0, 1-2, 6 months) series. This phase 3 study further assessed the immunogenicity and safety of the 2-dose MenB-FHbp schedule. METHODS: Subjects 10-25 years of age received MenB-FHbp (months 0, 6) and the quadrivalent meningococcal conjugate vaccine MenACWY-CRM (month 0). Primary immunogenicity endpoints included percentages of subjects achieving ≥ 4-fold increases from baseline in serum bactericidal antibody using human complement (hSBA) titers for 4 diverse, vaccine-heterologous primary serogroup B test strains and titers ≥ lower limit of quantitation (LLOQ; 1:8 or 1:16) for all 4 primary strains combined (composite response) after dose 2; a titer ≥ 1:4 is the accepted correlate of protection. Percentages of participants with hSBA titers ≥ LLOQ for 10 additional vaccine-heterologous strains were also assessed; positive predictive values of primary strain responses for secondary strain responses were determined. Safety was assessed. RESULTS: Overall, 1057 subjects received dose 1 and 946 received dose 2 of MenB-FHbp. Percentages of participants achieving ≥ 4-fold increases in hSBA titers against each primary strain after dose 2 ranged from 67.4% to 95.0% and the composite response was 74.3%. Primary strain responses were highly predictive of secondary strain responses. Most reactogenicity events were mild-to-moderate in severity and did not lead to withdrawal from the study. Adverse events (AEs) considered by the investigator to be related to vaccination occurred in 4.2% (44/1057) of subjects, and there were no serious AEs or newly diagnosed chronic medical conditions considered related to vaccination. CONCLUSIONS: MenB-FHbp administered at 0, 6 months was well tolerated and induced protective bactericidal antibody responses against diverse serogroup B strains. Findings provide further support for the continued use of MenB-FHbp on a 2-dose schedule in this population.
General Practice for Children and Adolescents Jindrichuv Hradec Czech Republic
Vaccine Clinical Research and Development Pfizer UK Hurley UK
Vaccine Medical and Scientific Affairs Pfizer Inc Collegeville PA USA
Vaccine Research and Development Pfizer Inc Brussels Belgium
Vaccine Research and Development Pfizer Inc Collegeville PA USA
Vaccine Research and Development Pfizer Inc Pearl River NY USA
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc22011284
- 003
- CZ-PrNML
- 005
- 20220506130213.0
- 007
- ta
- 008
- 220425s2022 ne f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.vaccine.2021.11.053 $2 doi
- 035 __
- $a (PubMed)34961633
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a ne
- 100 1_
- $a Drazan, Daniel $u General Practice for Children and Adolescents, Jindrichuv Hradec, Czech Republic
- 245 12
- $a A phase 3 study to assess the immunogenicity, safety, and tolerability of MenB-FHbp administered as a 2-dose schedule in adolescents and young adults / $c D. Drazan, H. Czajka, JD. Maguire, JL. Pregaldien, R. Maansson, R. O'Neill, AS. Anderson, P. Balmer, J. Beeslaar, JL. Perez
- 520 9_
- $a BACKGROUND: The MenB-FHbp vaccine is licensed to prevent meningococcal serogroup B disease on either a 2-dose (0, 6 months) or 3-dose (0, 1-2, 6 months) series. This phase 3 study further assessed the immunogenicity and safety of the 2-dose MenB-FHbp schedule. METHODS: Subjects 10-25 years of age received MenB-FHbp (months 0, 6) and the quadrivalent meningococcal conjugate vaccine MenACWY-CRM (month 0). Primary immunogenicity endpoints included percentages of subjects achieving ≥ 4-fold increases from baseline in serum bactericidal antibody using human complement (hSBA) titers for 4 diverse, vaccine-heterologous primary serogroup B test strains and titers ≥ lower limit of quantitation (LLOQ; 1:8 or 1:16) for all 4 primary strains combined (composite response) after dose 2; a titer ≥ 1:4 is the accepted correlate of protection. Percentages of participants with hSBA titers ≥ LLOQ for 10 additional vaccine-heterologous strains were also assessed; positive predictive values of primary strain responses for secondary strain responses were determined. Safety was assessed. RESULTS: Overall, 1057 subjects received dose 1 and 946 received dose 2 of MenB-FHbp. Percentages of participants achieving ≥ 4-fold increases in hSBA titers against each primary strain after dose 2 ranged from 67.4% to 95.0% and the composite response was 74.3%. Primary strain responses were highly predictive of secondary strain responses. Most reactogenicity events were mild-to-moderate in severity and did not lead to withdrawal from the study. Adverse events (AEs) considered by the investigator to be related to vaccination occurred in 4.2% (44/1057) of subjects, and there were no serious AEs or newly diagnosed chronic medical conditions considered related to vaccination. CONCLUSIONS: MenB-FHbp administered at 0, 6 months was well tolerated and induced protective bactericidal antibody responses against diverse serogroup B strains. Findings provide further support for the continued use of MenB-FHbp on a 2-dose schedule in this population.
- 650 _2
- $a mladiství $7 D000293
- 650 _2
- $a protilátky bakteriální $7 D000907
- 650 _2
- $a lidé $7 D006801
- 650 12
- $a meningokokové infekce $x prevence a kontrola $7 D008589
- 650 12
- $a meningokokové vakcíny $x škodlivé účinky $7 D022401
- 650 12
- $a Neisseria meningitidis $7 D009345
- 650 12
- $a Neisseria meningitidis séroskupiny B $7 D038541
- 650 _2
- $a séroskupina $7 D065288
- 650 _2
- $a vakcinace $7 D014611
- 650 _2
- $a mladý dospělý $7 D055815
- 655 _2
- $a klinické zkoušky, fáze III $7 D017428
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Czajka, Hanna $u Faculty of Medicine, University of Rzeszów, Rzeszów, Poland and Individual Specialist Medical Practice, Krakow, Poland
- 700 1_
- $a Maguire, Jason D $u Vaccine Research and Development, Pfizer Inc, Pearl River, NY, USA. Electronic address: Jason.Maguire@pfizer.com
- 700 1_
- $a Pregaldien, Jean-Louis $u Vaccine Research and Development, Pfizer Inc, Brussels, Belgium
- 700 1_
- $a Maansson, Roger $u Vaccine Research and Development, Pfizer Inc, Collegeville, PA, USA
- 700 1_
- $a O'Neill, Robert $u Vaccine Research and Development, Pfizer Inc, Pearl River, NY, USA
- 700 1_
- $a Anderson, Annaliesa S $u Vaccine Research and Development, Pfizer Inc, Pearl River, NY, USA
- 700 1_
- $a Balmer, Paul $u Vaccine Medical and Scientific Affairs, Pfizer Inc, Collegeville, PA, USA
- 700 1_
- $a Beeslaar, Johannes $u Vaccine Clinical Research and Development, Pfizer UK, Hurley, UK
- 700 1_
- $a Perez, John L $u Vaccine Research and Development, Pfizer Inc, Collegeville, PA, USA
- 773 0_
- $w MED00004631 $t Vaccine $x 1873-2518 $g Roč. 40, č. 2 (2022), s. 351-358
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/34961633 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y p $z 0
- 990 __
- $a 20220425 $b ABA008
- 991 __
- $a 20220506130206 $b ABA008
- 999 __
- $a ok $b bmc $g 1789068 $s 1162482
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2022 $b 40 $c 2 $d 351-358 $e 20211224 $i 1873-2518 $m Vaccine $n Vaccine $x MED00004631
- LZP __
- $a Pubmed-20220425
