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

RSV Infection Clinical Trial

Official title:
A Randomised, Phase 2a, Double-Blind, Placebo-Controlled Study to Evaluate the Safety and Prophylactic Efficacy of MV-012-968 Against Respiratory Syncytial Virus (RSV) Infection in the Virus Challenge Model.

Clinical Trial 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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04690335
Study type Interventional
Source Meissa Vaccines, Inc.
Contact
Status Completed
Phase Phase 2
Start date December 29, 2020
Completion date September 9, 2021
View Details
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