drugset / Trial / NCT06431607

A Study to Find the Dose and Assess the Immune Response and Safety of a Vaccine Against Influenza in Healthy Younger and Older Adults

NCT06431607

Phase 2 Completed 845 enrolled GlaxoSmithKline
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The purpose of this study is to assess the safety and immune response of GlaxoSmithKlines (GSK) messenger RNA (mRNA)-based multivalent vaccine (GSK4382276A) candidate against influenza, administered in healthy younger adults (YA) and older adults (OA).

Timeline

Start
2024-05-23
Primary completion
2024-12-27
Completion
2025-06-04

Drugs

EvaluationDrugModalityDoseRoute
Subject F2G22B/DL001Z Messenger RNA (mRNA) Intramuscular
Subject F2H23A/DL001Z-NH Messenger RNA (mRNA) Intramuscular
Subject F2H23B/DL001Z-NH Messenger RNA (mRNA) Intramuscular
Subject F2H23D/DL001Z-NH Messenger RNA (mRNA) Intramuscular
Subject F2H23G/DL001Z Messenger RNA (mRNA) Intramuscular
Subject F2H23H/DL001Z Messenger RNA (mRNA) Intramuscular
Subject FDQ23A-NH Vaccine Intramuscular
Subject Flu D-TIV Vaccine Intramuscular
Subject Fluzone HD Quadrivalent Vaccine Intramuscular
Subject GSK5800544A Messenger RNA (mRNA) Intramuscular
Subject Influenza Virus Vaccine Vaccine Intramuscular

Indications