Impact and Effectiveness of ABRYSVO® Vaccination During Pregnancy

Active, not recruitingOBSERVATIONAL
Enrollment

1

Participants

Timeline

Start Date

August 26, 2024

Primary Completion Date

October 1, 2026

Study Completion Date

October 1, 2026

Conditions
Respiratory Syncytial VirusRespiratory Tract Diseases
Interventions
BIOLOGICAL

ABRYSVO

"Test Negative Design: This is a non-interventional retrospective study; therefore, ABSYRVO vaccine has already been administered according to the standard of care. ABRYSVO is a bivalent RSV prefusion F protein-based vaccine (RSVpreF) composed of two prefusion F proteins to protect against both RSV-A and RSV-B.~Ecologic Before-and-After Design: This is an ecologic before-and-after study using aggregated data; as such, the 'exposure' of interest is time before ABRYSVO program implementation (i.e., five historical pre-ABRYSVO RSV seasons) and time after ABRYSVO implementation (i.e., post-ABRYSVO RSV seasons: 2024-2026)."

Trial Locations (1)

Unknown

Pfizer, Buenos Aires

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

iTrials S.A.

UNKNOWN

lead

Pfizer

INDUSTRY