drugset / Trial / NCT05975840

Safety and Immunogenicity of Different Formulations of Monovalent Influenza A/Astrakhan/3212/2020 Like (H5N8) Virus Vaccine With AS03 Adjuvant System in Medically Stable Adults

NCT05975840 ↗

Phase 1/2 Completed 518 enrolled GlaxoSmithKline
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The purpose of this study is to assess the safety and immunogenicity of different formulations of monovalent Influenza A/Astrakhan/3212/2020-like virus vaccine with AS03 adjuvant system in adults greater than or equal to (\>=)18 years of age.

Timeline

Start
2023-08-03
Primary completion
2024-05-21
Completion
2024-09-19

Drugs

EvaluationDrugModalityDoseRoute
Comparator FLU Q-PAN H5N8 375_A Vaccine 3.75 ug Intramuscular
Comparator FLU Q-PAN H5N8 375_B Vaccine 3.75 ug Intramuscular
Comparator FLU Q-PAN H5N8 750_A Vaccine 7.5 ug Intramuscular
Comparator FLU Q-PAN H5N8 750_B Vaccine 7.5 ug Intramuscular

Indications