drugset / Trial / NCT01704365

RSV-F Vaccine Dose Ranging Study in Young Women

NCT01704365

Phase 2 Completed 330 enrolled Novavax PATH · collab
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to evaluate the immunogenicty and safety of an RSV-F protein nanoparticle vaccine, with out without aluminum, in healthy women of child-bearing potential.

Timeline

Start
2012-10
Primary completion
2013-04
Completion
2013-05

Drugs

EvaluationDrugModalityDoseRoute
Subject RSV F vaccine Vaccine 60 ug Intramuscular
Subject RSV F vaccine Vaccine 90 ug Intramuscular