drugset / Trial / NCT05175950

Safety, Reactogenicity, and Immunogenicity Study of Heterologous Booster Vaccination of a SARS-CoV-2 Recombinant Protein Nanoparticle Vaccine (GBP510)

NCT05175950

RandomizedParallel-groupQuadruple-blindPrevention

Summary

This is randomized, placebo-controlled, observer-blinded, multi-center study to assess safety, reactogenicity and immunogenicity of booster vaccination of a SARS-CoV-2 recombinant protein nanoparticle vaccine (GBP510) adjuvanted with AS03 in adults aged 19 years and older who received a primary series of vaccination or the 1st booster vaccination against COVID-19 approved in Korea.

Timeline

Start
2022-01-24
Primary completion
2023-08
Completion
2023-11

Drugs

EvaluationDrugModalityDoseRoute
Subject GBP510 Vaccine 25 ug

Indications

No indication recorded.