TY - JOUR
T1 - Efficacy, safety and immunogenicity of a pneumococcal protein-based vaccine co-administered with 13-valent pneumococcal conjugate vaccine against acute otitis media in young children
T2 - A phase IIb randomized study
AU - Hammitt, Laura L.
AU - Campbell, James C.
AU - Borys, Dorota
AU - Weatherholtz, Robert C.
AU - Reid, Raymond
AU - Goklish, Novalene
AU - Moulton, Lawrence H.
AU - Traskine, Magali
AU - Song, Yue
AU - Swinnen, Kristien
AU - Santosham, Mathuram
AU - O'Brien, Katherine L.
N1 - Funding Information:
This study was funded by GlaxoSmithKline Biologicals SA.
Funding Information:
The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: [ Potential Conflict of interest: L.L. Hammitt, J.C. Campbell, R.C. Weatherholtz, R. Reid, M. Santosham and K.L. O’Brien report institutional research grants from the GSK group of companies, during the conduct of the study. L.L. Hammitt, R.C. Weatherholtz and K.L. O’Brien also report institutional grants from Pfizer, Novavax and Merck outside the submitted work. M. Santosham also reports an institutional research grant for Rota Council from the GSK group of companies. K.L. O’Brien also reports to be an external scientific advisor for Pfizer, Sanofi Pasteur, Merck and the GSK group of companies. L.H. Moulton reports personal fees from a Merck Scientific Advisory Board outside the submitted work. N. Goklish has no conflict of interest to disclose. M. Traskine, K. Swinnen and D. Borys are employees of the GSK group of companies, and K. Swinnen and D. Borys hold shares of the GSK group of companies. Y. Song worked for XPE Pharma & Science as a consultant for the GSK group of companies.]
Publisher Copyright:
© 2019 The Authors
Copyright:
Copyright 2019 Elsevier B.V., All rights reserved.
PY - 2019/12/3
Y1 - 2019/12/3
N2 - Background: Native American populations experience a substantial burden of pneumococcal disease despite use of highly effective pneumococcal conjugate vaccines (PCVs). Protein-based pneumococcal vaccines may extend protection beyond the serotype-specific protection elicited by PCVs. Methods: In this phase IIb, double-blind, controlled trial, 6–12 weeks-old Native American infants randomized 1:1, received either a protein-based pneumococcal vaccine (dPly/PhtD) containing pneumolysin toxoid (dPly, 10 µg) and pneumococcal histidine triad protein D (PhtD, 10 µg) or placebo, administered along with 13-valent PCV (PCV13) at ages 2, 4, 6 and 12–15 months. Other pediatric vaccines were given per the routine immunization schedule. We assessed vaccine efficacy (VE) against acute otitis media (AOM) and acute lower respiratory tract infection (ALRI) endpoints. Immunogenicity, reactogenicity and unsolicited adverse events were assessed in a sub-cohort and serious adverse events were assessed in all children. Results: 1803 infants were randomized (900 dPly/PhtD; 903 Control). VE against all episodes of American Academy of Pediatrics (AAP)-defined AOM was 3.8% (95% confidence interval: −11.4, 16.9). Point estimates of VE against other AOM outcomes ranged between 2.9% (−9.5, 14.0) and 5.2% (−8.0, 16.8). Point estimates of VE against ALRI outcomes ranged between −4.4% (−39.2, 21.8) and 2.0% (−18.3, 18.8). Point estimates of VE tended to be higher against first than all episodes but the confidence intervals included zero. dPly/PhtD vaccine was immunogenic and had an acceptable reactogenicity and safety profile after primary and booster vaccination in Native American infants. Conclusions: The dPly/PhtD vaccine was immunogenic and well tolerated, however, incremental efficacy in preventing AAP-AOM over PCV13 was not demonstrated. Clinical trials registration: NCT01545375 (www.clinicaltrials.gov)
AB - Background: Native American populations experience a substantial burden of pneumococcal disease despite use of highly effective pneumococcal conjugate vaccines (PCVs). Protein-based pneumococcal vaccines may extend protection beyond the serotype-specific protection elicited by PCVs. Methods: In this phase IIb, double-blind, controlled trial, 6–12 weeks-old Native American infants randomized 1:1, received either a protein-based pneumococcal vaccine (dPly/PhtD) containing pneumolysin toxoid (dPly, 10 µg) and pneumococcal histidine triad protein D (PhtD, 10 µg) or placebo, administered along with 13-valent PCV (PCV13) at ages 2, 4, 6 and 12–15 months. Other pediatric vaccines were given per the routine immunization schedule. We assessed vaccine efficacy (VE) against acute otitis media (AOM) and acute lower respiratory tract infection (ALRI) endpoints. Immunogenicity, reactogenicity and unsolicited adverse events were assessed in a sub-cohort and serious adverse events were assessed in all children. Results: 1803 infants were randomized (900 dPly/PhtD; 903 Control). VE against all episodes of American Academy of Pediatrics (AAP)-defined AOM was 3.8% (95% confidence interval: −11.4, 16.9). Point estimates of VE against other AOM outcomes ranged between 2.9% (−9.5, 14.0) and 5.2% (−8.0, 16.8). Point estimates of VE against ALRI outcomes ranged between −4.4% (−39.2, 21.8) and 2.0% (−18.3, 18.8). Point estimates of VE tended to be higher against first than all episodes but the confidence intervals included zero. dPly/PhtD vaccine was immunogenic and had an acceptable reactogenicity and safety profile after primary and booster vaccination in Native American infants. Conclusions: The dPly/PhtD vaccine was immunogenic and well tolerated, however, incremental efficacy in preventing AAP-AOM over PCV13 was not demonstrated. Clinical trials registration: NCT01545375 (www.clinicaltrials.gov)
KW - Acute otitis media
KW - Immunogenicity
KW - Native American
KW - Reactogenicity
KW - Streptococcus pneumoniae
KW - Vaccines
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U2 - 10.1016/j.vaccine.2019.09.076
DO - 10.1016/j.vaccine.2019.09.076
M3 - Article
C2 - 31629570
AN - SCOPUS:85074104421
SN - 0264-410X
VL - 37
SP - 7482
EP - 7492
JO - Vaccine
JF - Vaccine
IS - 51
ER -