drugset / Trial / NCT03387137

Evaluating the Infectivity, Safety, and Immunogenicity of a Respiratory Syncytial Virus Vaccine (RSV 6120/∆NS2/1030s) in RSV-Seropositive Children and RSV-Seronegative Infants and Children

NCT03387137 ↗

RandomizedParallel-groupQuadruple-blindPrevention

Summary

The purpose of this study is to evaluate the infectivity, safety, and immunogenicity of a single dose of a recombinant, live-attenuated respiratory syncytial virus (RSV) vaccine (RSV 6120/∆NS2/1030s) in RSV-seropositive children 12 to 59 months of age and RSV-seronegative infants and children 6 to 24 months of age.

Timeline

Start
2017-10-13
Primary completion
2019-11-22
Completion
2021-05-31

Drugs

EvaluationDrugModalityDoseRoute
Subject RSV 6120/∆NS2/1030s Vaccine 100000 unknown Intranasal
Subject RSV 6120/∆NS2/1030s Vaccine 501187 unknown Intranasal