drugset / Trial / NCT04785612

Study of RSVpreF Vaccination and RSV Challenge in Healthy Adults

NCT04785612

Phase 2 Completed 70 enrolled Hvivo Pfizer · collab
RandomizedParallel-groupQuadruple-blindPrevention

Summary

In this randomised, placebo-controlled, double-blind Phase 2a study, healthy male and female participants 18-50 years of age will be given an investigational RSV vaccine (RSVpreF) and challenged with RSV one month later. The purpose of this research study is to assess the safety, immunogenicity and efficacy of RSVpreF using a human viral challenge model.

Timeline

Start
2020-11-10
Primary completion
2021-04-08
Completion
2021-08-16

Drugs

EvaluationDrugModalityDoseRoute
Subject RSVpreF Vaccine 120 ug