drugset / Trial / NCT03275389

A Study to Evaluate the Reactogenicity, Safety and Immunogenicity of GlaxoSmithKline (GSK) Biologicals' Investigational Supra-seasonal Universal Influenza Vaccines - Inactivated (SUIVs) (GSK3816302A) in Healthy Adults Aged 18 to 39 Years

NCT03275389

Phase 1 Completed 470 enrolled GlaxoSmithKline
RandomizedParallel-groupTriple-blindPrevention

Summary

The purpose of this study is to assess the reactogenicity, safety and immunogenicity of different formulations of GlaxoSmithKline (GSK) Biologicals' investigational supra-seasonal universal influenza vaccines (SUIVs) (unadjuvanted or adjuvanted) in 18 to 39 year-old healthy subjects. Subjects will be enrolled and vaccinated with one or 2 primary dose(s) followed by a booster dose one year later.

Timeline

Start
2017-09-08
Primary completion
2020-03-26
Completion
2020-03-26

Drugs

EvaluationDrugModalityDoseRoute
Subject AS03 Other / unclassified 15 ug Intramuscular
Subject D-SUIV cH11/1N1 Unknown 15 ug Intramuscular
Subject D-SUIV cH11/1N1+AS01 Unknown 15 ug Intramuscular
Subject D-SUIV cH11/1N1+AS03 Unknown 15 ug Intramuscular
Subject D-SUIV cH5/1N1 Unknown 15 ug Intramuscular
Subject D-SUIV cH5/1N1+AS01 Unknown 15 ug Intramuscular
Subject D-SUIV cH5/1N1+AS03 Unknown 15 ug Intramuscular
Subject D-SUIV cH8/1N1 Unknown 15 ug Intramuscular
Subject D-SUIV cH8/1N1+AS01 Unknown 15 ug Intramuscular
Comparator Fluarix Quadrivalent Vaccine Intramuscular

Indications