A phase 4 study of the safety of the 13-valent pneumococcal conjugate vaccine in children 6 to 17 years of age in India.


Journal

Vaccine
ISSN: 1873-2518
Titre abrégé: Vaccine
Pays: Netherlands
ID NLM: 8406899

Informations de publication

Date de publication:
31 08 2021
Historique:
received: 21 12 2020
revised: 23 06 2021
accepted: 20 07 2021
pubmed: 10 8 2021
medline: 25 2 2023
entrez: 9 8 2021
Statut: ppublish

Résumé

The 13-valent pneumococcal conjugate vaccine (PCV13) was recently approved in India for the prevention of pneumococcal disease in children aged 6 to 17 years based on global data as well as immunogenicity and safety findings from a phase 3 study. The current phase 4 study in India further evaluated the safety profile of PCV13 in this age group to support the positive benefit-risk profile of PCV13. Healthy male and female children aged 6 to 17 years in India were administered a single intramuscular injection of PCV13. Through 7 days after PCV13 administration, local reactions and systemic events were recorded daily by caregivers in an electronic diary. Adverse events (AEs) were collected from the provision of informed consent through 28-42 days postvaccination. One hundred subjects enrolled in and completed the study. After PCV13 vaccination, 73.9% and 57.8% of subjects reported local reactions and systemic events, respectively. The majority of reactogenicity events were mild to moderate in severity, with injection site pain and fatigue the most frequently reported local reaction and systemic event, respectively. Six subjects reported 7 AEs, all of which were considered unrelated to PCV13. One subject reported a serious AE (acute hepatitis), which was considered unrelated to PCV13 and ultimately resolved. No subjects withdrew because of AEs, and there were no deaths. PCV13 vaccination was well tolerated with an acceptable safety profile in healthy subjects aged 6 to 17 years in India. This work further supports the safety profile of PCV13 for prevention of pneumococcal disease in this age group in India.

Identifiants

pubmed: 34366142
pii: S0264-410X(21)00946-4
doi: 10.1016/j.vaccine.2021.07.055
pii:
doi:

Substances chimiques

Vaccines, Conjugate 0

Types de publication

Clinical Trial, Phase IV Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

5313-5317

Informations de copyright

Copyright © 2021 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest R Chand, K Yi, S Suroju, DA Scott, and S Lockhart are employees of Pfizer Inc and may hold stock or stock options. J Chhatwal, A Sapru, B Sundaram, and B Shenoy received research funding from Pfizer Inc to conduct the study.

Auteurs

Jugesh Chhatwal (J)

Department of Paediatric Medicine, Christian Medical College, Ludhiana, Punjab, India.

Amita Sapru (A)

Department of Paediatrics, KEM Hospital Research Centre, Pune, Maharashtra, India.

Balasubramanian Sundaram (B)

Department of Paediatrics, Kanchi Kamakoti CHILDS Trust Hospital, Chennai, Tamil Nadu, India.

Bhaskar Shenoy (B)

Department of Paediatrics, Manipal Hospital, Bengaluru, Karnataka, India.

Rohit Chand (R)

Global Site and Study Operations, Pfizer Ltd, Mumbai, India.

Kevin Yi (K)

Medical Development - Vaccines, Pfizer Inc, Collegeville, PA, USA.

Suresh Suroju (S)

Vaccine Clinical Research and Development, Pfizer Ltd, Hurley, UK.

Daniel A Scott (DA)

Vaccine Clinical Research and Development, Pfizer Inc, Collegeville, PA, USA.

Stephen Lockhart (S)

Vaccine Clinical Research and Development, Pfizer Ltd, Hurley, UK. Electronic address: stephen.p.lockhart@pfizer.com.

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Classifications MeSH