Safety and immunogenicity of a multidose vial formulation of 13-valent pneumococcal conjugate vaccine administered with routine pediatric vaccines in healthy infants in India: A phase 4, randomized, open-label study.


Journal

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

Informations de publication

Date de publication:
05 11 2021
Historique:
received: 16 06 2021
revised: 07 09 2021
accepted: 09 09 2021
pubmed: 18 10 2021
medline: 27 1 2022
entrez: 17 10 2021
Statut: ppublish

Résumé

This phase 4, randomized, open-label, multicenter study in healthy Indian infants and toddlers evaluated the safety, tolerability, and immunogenicity of the 13-valent pneumococcal conjugate vaccine (PCV13) formulated in a multidose vial (MDV) or single prefilled syringe (PFS). Healthy Indian infants (6 weeks of age) were randomized 1:1 to receive either PCV13-MDV or PCV13-PFS concomitant with routine pediatric vaccines. Subjects received a single dose of either PCV13-MDV or PCV13-PFS as a 4-dose schedule (infant series: 1 dose at 6, 10, and 14 weeks of age; toddler dose: 12 months of age). Safety was assessed, including local reactions, systemic events, and adverse events (AEs). Immunogenicity 1 month after both the infant series and toddler dose was measured by concentrations of serotype-specific immunoglobulin G (IgG) antibodies and opsonophagocytic activity titers. Rates and severities of local reactions and systemic events up to 7 days after each dose of either PCV13-MDV or PCV13-PFS were generally similar, with the majority being of mild or moderate severity. PCV13-MDV had a safety profile comparable with PCV13-PFS; both groups experienced a similar frequency of AEs. PCV13-MDV elicited immune responses comparable with those induced by PCV13-PFS. Clear boosting of immune responses after the PCV13-MDV toddler dose was observed; ≥96% of subjects showed serotype-specific IgG concentrations at or above the defined thresholds 1 month after the PCV13-MDV toddler dose. PCV13-MDV was safe, well tolerated, and immunogenic in healthy Indian infants and toddlers when coadministered with routine pediatric vaccinations. Safety and immunogenicity of PCV13-MDV was comparable with PCV13-PFS. Clinicaltrials.gov: NCT03548337.

Identifiants

pubmed: 34656378
pii: S0264-410X(21)01208-1
doi: 10.1016/j.vaccine.2021.09.029
pii:
doi:

Substances chimiques

Antibodies, Bacterial 0
Heptavalent Pneumococcal Conjugate Vaccine 0
Pneumococcal Vaccines 0
Vaccines, Conjugate 0

Banques de données

ClinicalTrials.gov
['NCT03548337']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

6787-6795

Informations de copyright

Copyright © 2021 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: WK, RC, MD, SS, DAS, and SPL are current employees of Pfizer Inc and may hold stock or stock options. PVR does not have any conflicts of interest to report. AS receives professional fees from the KEM Hospital Research Centre, Pune for her role as investigator in studies funded by Pfizer.

Auteurs

Sanjay Kewalchand Lalwani (SK)

Department of Pediatrics, Bharati Vidyapeeth Medical College and Hospital, Pune, Maharashtra, India.

Padmasani Venkat Ramanan (PV)

Department of Pediatrics, Sri Ramachandra Hospital, Chennai, Tamil Nadu, India.

Amita Sapru (A)

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

Balasubramanian Sundaram (B)

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

Bela Hasmukh Shah (BH)

Department of Pediatrics, B.J. Medical College and Civil Hospital, Ahmedabad, Gujarat, India.

Dinesh Kaul (D)

Department of Pediatrics, Sir Ganga Ram Hospital, New Delhi, India.

N Karthik Nagesh (N)

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

Warren V Kalina (WV)

Vaccine Research and Development, Pfizer Inc, Pearl River, New York, USA.

Rohit Chand (R)

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

Meichun Ding (M)

Vaccine Research and Development, Pfizer Inc, Pearl River, New York, 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 P Lockhart (SP)

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

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH