drugset / Trial / NCT02624947

A Study to Determine the Safety and Efficacy of the RSV F Vaccine to Protect Infants Via Maternal Immunization

NCT02624947

Phase 3 Completed 4636 enrolled Novavax Bill and Melinda Gates Foundation · collab
RandomizedParallel-groupTriple-blindPrevention

Summary

The purpose of this study is to determine the efficacy of maternal immunization during the third trimester of pregnancy with the RSV F vaccine against medically-significant RSV lower respiratory tract infection (LRTI), as defined by hypoxemia or tachypnea at rest, through the first 90, 120, 150, and 180 days of life in infants.

Timeline

Start
2015-12
Primary completion
2018-12-28
Completion
2019-07-12

Drugs

EvaluationDrugModalityDoseRoute
Comparator RSV F vaccine Vaccine 0.5 ml Intramuscular