A Study on the Safety and Immune Response to an Unadjuvanted RSV Maternal Vaccine, in High Risk Pregnant Women Aged 15 to 49 Years and Infants Born to the Vaccinated Mothers
Stopped Following a recommendation from the Independent Data Monitoring Committee of NCT04605159 (RSV MAT 009), GSK made the decision to stop enrolment and vaccination in the study.
Conditions
- Respiratory Syncytial Virus Infections
Interventions
- BIOLOGICAL: RSV MAT
- DRUG: Placebo
Sponsor
GlaxoSmithKline