Trial intelligence / Profile preview

RSV_IMPACT: ABRYSVO Vaccine in Pregnant Women for RSV Prevention in Infants

NCT06955728Phase 3Recruiting

Sponsor
University of the Witwatersrand
Start
Sep 2025
Primary completion
Feb 2028
Modality
Vaccines & Immunotherapeutics
Countries
4
01

Overview

Phase 3, randomised, double-blind trial in respiratory syncytial virus infection (RSV) comparing Placebo with ABRYSVO (2 arms). Primary endpoints: Efficacy against RSV-A or RSV-B subtype confirmed severe LRTI at 180 days and Occurrence of preterm births (<37 weeks GA). Started Sep 2025; status: recruiting.

02

Drugs

RSVpreF vaccine
03

Conditions

respiratory syncytial virus infection (RSV)

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