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A Phase 3, Randomized, Double Blinded, Placebo Controlled Trial to Evaluate the Efficacy and Safety of a Respiratory Syncytial Virus (RSV) Prefusion F Subunit Vaccine in Infants Born to Women Vaccinated During Pregnancy

This study is designed to evaluate the efficacy and safety of maternal immunization with RSVpreF against medically attended lower respiratory tract illness in infants.
Erin Hammett at
18 year(s) or older
This study is also accepting healthy volunteers
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Inclusion Criteria:
Healthy pregnant women age 49 or less
No significant fetal anomalies noted on ultrasound at at least 18 weeks gestation
HIV, syphilis, and hepatitis b negative
Planning to deliver at Hershey Medical Center
Willing to consent for infant to participate in study
Exclusion Criteria:
Pre-pregnancy BMI >40
History of severe adverse/allergic reaction to vaccination
Current pregnancy resulting from in vitro fertilization
Current or past pregnancy complications or abnormalities
Prevention, Children's Health, Pregnancy & Infertility
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Hershey, PA