drugset / Trial / NCT07768345

A Study to Learn About Revaccination With a Vaccine Called RSVpreF in Immunocompromised Adults

NCT07768345 ↗

Phase 3 Recruiting 440 enrolled Pfizer
Non-randomizedParallel-groupOpen-labelPrevention

Summary

The purpose of this phase 3 study is to learn the safety, tolerability and immunogenicity of revaccination with RSVpreF at approximately 1-, 2-, and 3-year intervals to inform the revaccination interval in immunocompromised adults. This study is seeking participants who are 18 years of age and older and will be grouped based on prior RSV vaccination history. Participants are required to be immunocompromised per study protocol. All participants in this study will receive 1 shot to their arm of a RSVPreF vaccine. Participants will take part in this study for about 12 months and will need to visit the clinical study site at least 4 times.

Timeline

Start
2026-08-31
Primary completion
2028-02-02
Completion
2028-02-02

Drugs

EvaluationDrugModalityDoseRoute
Subject RSVpreF Vaccine — —