drugset / Trial / NCT05364242

VLA2001 Booster in Adult Participants After Priming With mRNA COVID-19 Vaccine and/or Natural SARS-CoV-2 Infection

NCT05364242

Phase 2/3 Completed 178 enrolled Valneva Austria GmbH
NaSingle-groupOpen-labelPrevention

Summary

This is a clinical study to investigate the safety, tolerability and immunogenicity of a VLA2001 booster vaccination in participants aged 18 years and older. In total approximately 275 participants are planned to be enrolled.

Timeline

Start
2022-05-09
Primary completion
2022-09-22
Completion
2023-05-22

Drugs

EvaluationDrugModalityDoseRoute
Subject VLA2001 Vaccine