Fully Liquid MenACWY-CRM Vaccine: Results from an Integrated Safety Analysis.


Journal

Drug safety
ISSN: 1179-1942
Titre abrégé: Drug Saf
Pays: New Zealand
ID NLM: 9002928

Informations de publication

Date de publication:
01 2023
Historique:
accepted: 19 09 2022
pubmed: 13 11 2022
medline: 12 1 2023
entrez: 12 11 2022
Statut: ppublish

Résumé

The currently licensed quadrivalent MenACWY-CRM conjugate vaccine presentation consists of two vials (lyophilized MenA and liquid MenCWY) to be reconstituted before injection. A new fully liquid, single-vial formulation has been developed to simplify administration and prevent reconstitution errors. We present pooled safety data from two randomized, controlled, observer-blind phase 2b clinical trials, in which the fully liquid presentation was compared with the licensed presentation. This is a post hoc analysis of two studies, in which safety data from participants aged 10-40 years who received one dose of either liquid MenACWY-CRM (1337 participants; MenACWY liquid group) or licensed MenACWY-CRM (1332 participants; MenACWY licensed group) were pooled. Frequencies were calculated for solicited adverse events (AEs) during 7 days post-vaccination and unsolicited AEs, including medically attended AEs and serious AEs (SAEs), during the 6-month safety follow-up period. Analysis results are presented by vaccine group, overall and by age category (10-17 and 18-40 years). Overall, AEs solicited for collection during the first 7 days after vaccination were reported by similar percentages of participants (69.2%, MenACWY liquid; 68.2%, MenACWY licensed), and were generally mild/moderate in intensity. Solicited local AEs were reported by 46.0% of the MenACWY liquid group and 43.5% of the MenACWY licensed group and solicited systemic AEs by 55.2 and 54.1%, respectively. During the 6-month post-vaccination period, unsolicited AEs were reported by 32.2 and 31.2% of the MenACWY liquid group and MenACWY licensed group, respectively, and medically attended AEs by 18.6 and 17.3%, respectively. Overall, 14 participants in each group (1.0 and 1.1%, respectively) reported SAEs, none of which was considered vaccine-related by the investigator. The safety profiles of both MenACWY-CRM presentations were similar for each age group and overall. This pooled analysis shows the safety profile of fully liquid MenACWY-CRM is comparable with that of the currently licensed vaccine presentation. ClinicalTrials.gov Identifiers: NCT03652610 (August 29, 2018), NCT03433482 (14 February 2018).

Identifiants

pubmed: 36369456
doi: 10.1007/s40264-022-01242-8
pii: 10.1007/s40264-022-01242-8
pmc: PMC9829640
doi:

Substances chimiques

MenACWY-CRM vaccine 0

Banques de données

ClinicalTrials.gov
['NCT03652610', 'NCT03433482', 'NCT03652610']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

99-108

Informations de copyright

© 2022. GSK.

Références

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Auteurs

Puneet Vir Singh (P)

GSK, Safety Evaluation and Risk Management, Siena, Italy.

Paola Tiberi (P)

GSK, Safety Evaluation and Risk Management, Siena, Italy.

Gabriele Filippo Di Domenico (GF)

GSK, Biostatistics and Statistical Programming, Siena, Italy.

Valerio Romolini (V)

GSK, Biostatistics and Statistical Programming, Siena, Italy.

Thembile Mzolo (T)

GSK, Biostatistics, Amsterdam, The Netherlands.

Marco Costantini (M)

GSK, Biostatistics and Statistical Programming, Siena, Italy.

Tauseefullah Akhund (T)

GSK, Clinical Research and Development Centre, Siena, Italy.

Venere Basile (V)

GSK, Global Clinical Operations, Siena, Italy.

Maria Lattanzi (M)

GSK, Clinical Research and Development Centre, Siena, Italy.

Michele Pellegrini (M)

GSK, Clinical Research and Development Centre, Siena, Italy. michele.x.pellegrini@gsk.com.

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