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
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | RSV 6120/∆NS2/1030s | Vaccine | 100000 unknown | Intranasal |
| Subject | RSV 6120/∆NS2/1030s | Vaccine | 501187 unknown | Intranasal |