drugset / Trial / NCT05252338

A Study to Evaluate the Safety, Reactogenicity and Immunogenicity of Vaccine CVSQIV in Healthy Adults

NCT05252338 ↗

Phase 1 Completed 240 enrolled CureVac GlaxoSmithKline · collab
Non-randomizedSequentialOpen-labelPrevention

Summary

This study aims to evaluate the safety and reactogenicity profile of CVSQIV at different dose levels.

Timeline

Start
2022-02-07
Primary completion
2022-09-27
Completion
2022-09-27

Drugs

EvaluationDrugModalityDoseRoute
Subject CVSQIV Messenger RNA (mRNA) 3 ug Intramuscular
Subject CVSQIV Messenger RNA (mRNA) 6 ug Intramuscular
Subject CVSQIV Messenger RNA (mRNA) 12 ug Intramuscular
Subject CVSQIV Messenger RNA (mRNA) 20 ug Intramuscular
Subject CVSQIV Messenger RNA (mRNA) 28 ug Intramuscular

Indications