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

Purpose

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.

Condition

  • Respiratory Syncytial Virus (RSV)

Eligibility

Eligible Ages
Over 18 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Participants ≥18 years of age who are/were immunocompromised at the time of initial RSVpreF vaccination, per study protocol, and will be grouped based on prior RSV vaccination history: - Group 1 will include participants naïve to any RSV vaccine. - Group 2 will include participants who received a single prior dose of RSVpreF (Abrysvo) approximately 1 year (9 to 15 months) prior to enrollment. - Group 3 will include participants who received a single prior dose of RSVpreF (Abrysvo) approximately 2 years (21 to 27 months) prior to enrollment. - Group 4 will include participants who previously received 2 doses of RSVpreF in Study C3671023 Substudy B approximately 3 years (36 to 42 months) prior to enrollment. - Participants should have a life expectancy ≥12 months (365 days) in the opinion of the investigator at enrollment.

Exclusion Criteria

  • Prior history of any subtype of Guillain-Barré Syndrome (GBS) of any etiology. - History of severe adverse reaction associated with a vaccine and/or severe allergic reaction (eg, anaphylaxis) to any components of the study intervention(s). - Participants with a history of transplant rejection, or PTLD, or participants who have had treatment for these conditions, within 90 days prior to study enrollment or suspected chronic humoral or cellular rejection. - Receipt of B-cell depleting therapies within 180 days prior to initial study vaccination. Refer to the study contact for further eligibility details.

Study Design

Phase
Phase 3
Study Type
Interventional
Allocation
Non-Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Prevention
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Group 1 		RSVpreF Vaccine
  • Biological: RSVpreF Vaccine
    RSVpreF Vaccine
Experimental
Group 2 		RSVpreF Vaccine
  • Biological: RSVpreF Vaccine
    RSVpreF Vaccine
Experimental
Group 3 		RSVpreF Vaccine
  • Biological: RSVpreF Vaccine
    RSVpreF Vaccine
Experimental
Group 4 		RSVpreF Vaccine
  • Biological: RSVpreF Vaccine
    RSVpreF Vaccine

Recruiting Locations

Kaiser Foundation Hospital LAMC
Los Angeles, California 90027

Kaiser Permanente Los Angeles Medical center
Los Angeles, California 90027

Kaiser Permanente
Los Angeles, California 90027

More Details

Status
Recruiting
Sponsor
Pfizer

Study Contact

Pfizer CT.gov Call Center
1-800-718-1021
ClinicalTrials.gov_Inquiries@pfizer.com