A Study to Learn Safety and Immune Response to Study Vaccine -RSVpreF in Adults at High Risk of Severe RSV Disease.

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18-59
SponsorPfizer

About this trial

The purpose of the study is to learn about the immune response after a RSVpreF vaccination. This study is being conducted in Japan. RSV is a common virus that can cause infections of the lungs and airways.

The study is seeking participants who are:

* 18 to 59 years of age * adults with health condition(s) that can put them at an increased risk of severe RSV disease

It will also learn about the safety of RSVpreF vaccination. The study lasts about 2 months. Adults need to visit the research site at least 2 times. The participant will receive a phone call 2 months after vaccination for health checks.

Eligibility criteria

Qualifiers

None

Disqualifiers

Received any kind of RSV vaccine before participating in this study

Determined as not eligible by the investigator based on the participant's past and present health condition(s), medication(s) and treatment(s)

Trial design

Treatments tested in this trial

  • RSVpreF

Treatment groups

130 Participants
are divided into 1 treatment group

Sponsors and collaborators