drugset / Trial / NCT03392389

Safety, Reactogenicity, and Immunogenicity of mRNA-1653 in Healthy Adults

NCT03392389 ↗

Phase 1 Completed 124 enrolled ModernaTX, Inc.
RandomizedSequentialDouble-blindPrevention

Summary

This clinical study will assess the safety, reactogenicity and immunogenicity of mRNA-1653, a combined human metapneumovirus and human parainfluenza virus type 3 vaccine in healthy adults.

Timeline

Start
2017-12-04
Primary completion
2019-07-29
Completion
2019-07-29

Drugs

EvaluationDrugModalityDoseRoute
Subject mRNA-1653 Vaccine — —