drugset / Trial / NCT04690335

Human Challenge Study to Evaluate the Efficacy of MV-012-968 Vaccine

NCT04690335 ↗

Phase 2 Completed 60 enrolled Meissa Vaccines, Inc. Hvivo · collab
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The purpose of this research study is to evaluate whether the investigational, live attenuated, intranasally delivered vaccine MV-012-968 ('study vaccine') may have prophylactic efficacy against symptomatic RSV infection when administered to adults 18-45 years of age in the Human Viral Challenge model.

Timeline

Start
2020-12-29
Primary completion
2021-05-07
Completion
2021-09-09

Drugs

EvaluationDrugModalityDoseRoute
Subject MV-012-968 Vaccine 1e+06 unknown Intranasal