drugset / Trial / NCT05960097

A Study on the Safety and Immune Response of Investigational COVID-19 mRNA Vaccines in Healthy Adults

NCT05960097 ↗

Phase 2 Completed 692 enrolled GlaxoSmithKline CureVac · collab
RandomizedParallel-groupTriple-blindPrevention

Summary

The purpose of Part A of this study is to assess the immune response and safety of a booster dose of investigational COVID-19 mRNA vaccines in healthy adults. The study will compare the investigational vaccines to control vaccine. The purpose of Part B of this study is to assess the immune response and safety of a booster dose of investigational COVID-19 mRNA vaccines in healthy adults. The study will compare the investigational vaccine under three different storage conditions.

Timeline

Start
2023-08-01
Primary completion
2024-08-30
Completion
2024-08-30

Drugs

EvaluationDrugModalityDoseRoute
Subject CV0601 Unknown — Intramuscular
Subject CV0701 Unknown — Intramuscular
Subject CV0801 Unknown — Intramuscular

Indications