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RecruitingRespiratory Syncytial Virus (RSV)

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

Eligible age

18+ yrs

Accepts

All genders

Locations

6 states

Healthy volunteers

No

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About this study

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.

Sponsor: Pfizer

Where it's recruiting

California

Los Angeles

District of Columbia

Washington D.C.

Georgia

Decatur

New York

New York · Rochester

Pennsylvania

Duncansville

Source: ClinicalTrials.gov · NCT07768345 · last updated 2026-09-25