Effectiveness of ABRYSVO® Maternal Respiratory Syncytial Virus (RSV) Vaccine Against RSV in Infants in Western Pennsylvania

Active, not recruitingOBSERVATIONAL
Enrollment

1

Participants

Timeline

Start Date

February 24, 2025

Primary Completion Date

July 31, 2027

Study Completion Date

July 31, 2027

Conditions
Respiratory Syncytial Viruses
Interventions
BIOLOGICAL

ABRYSVO Vaccination

"The primary exposure of interest for the TND study is maternal history of vaccination with Pfizer's ABRYSVO vaccine during pregnancy with the infant who presented for care. Infants will be considered exposed to ABRYSVO if their birth parent has documented evidence of receiving ABRYSVO ≥14 days before the date of the infant's birth, during the licensed gestational age window of 32 0/7 to 36 6/7 weeks."

Trial Locations (1)

10001

Pfizer, New York

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY

NCT06813872 - Effectiveness of ABRYSVO® Maternal Respiratory Syncytial Virus (RSV) Vaccine Against RSV in Infants in Western Pennsylvania | Biotech Hunter | Biotech Hunter