drugset / Trial / NCT05105048

A Study to Evaluate the Safety, Reactogenicity, and Immunogenicity of Cytomegalovirus (CMV) Vaccine mRNA-1647

NCT05105048

Phase 1 Completed 9 enrolled ModernaTX, Inc.
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The main objective of this study is to evaluate the safety, reactogenicity, and immunogenicity of the mRNA-1647 vaccine administered according to a 3-study injection schedule in healthy cytomegalovirus (CMV)-seronegative and CMV-seropositive Japanese adults 18 to 40 years of age in the United States.

Timeline

Start
2021-11-08
Primary completion
2023-08-10
Completion
2023-08-10

Drugs

EvaluationDrugModalityDoseRoute
Subject mRNA-1647 Messenger RNA (mRNA) Intramuscular