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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Clinical Lot Consistency for RSVpreF in a Population of Healthy Adults 18 to ≤49 Years of Age

ClinicalTrials.gov ID: NCT05096208

Public ClinicalTrials.gov record NCT05096208. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 17, 2026, 3:22 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A PHASE 3, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO EVALUATE THE SAFETY, TOLERABILITY, AND IMMUNOGENICITY OF 3 LOTS OF RESPIRATORY SYNCYTIAL VIRUS (RSV) PREFUSION F SUBUNIT VACCINE IN HEALTHY ADULTS

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This randomized, double-blinded, placebo-controlled Phase 3 study is designed to evaluate the safety, tolerability, and immunogenicity of 3 lots of RSVpreF in healthy adults.

Study identification

NCT ID
NCT05096208
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer
Industry
Enrollment
1,028 participants

Conditions and interventions

Conditions

Interventions

Biological

Eligibility (public fields only)

Age range
18 Years to 49 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 21, 2021 (Actual)
Primary completion
Apr 4, 2022 (Actual)
Completion
Apr 4, 2022 (Actual)
Last update posted
Apr 12, 2023

2021 – 2022

United States locations

U.S. sites
18
U.S. states
12
U.S. cities
16
Facility City State ZIP Site status
Global Health Research Center, Inc. Miami Lakes Florida 33016 —
Precision Clinical Research Sunrise Florida 33351 —
Clinical Site Partners, Inc Winter Park Florida 32789 —
Clinical Site Partners Winter Park Florida 32789 —
Clinical Research Atlanta Stockbridge Georgia 30281 —
East-West Medical Research Institute Honolulu Hawaii 96814 —
Clinical Research Prime Idaho Falls Idaho 83404 —
Kentucky Pediatric/ Adult Research Bardstown Kentucky 40004 —
Sundance Clinical Research St Louis Missouri 63141 —
Meridian Clinical Research, LLC Omaha Nebraska 68134 —
Accellacare - Wilmington Wilmington North Carolina 28401 —
Aventiv Research Inc Columbus Ohio 43213 —
Velocity Clinical Research, Providence East Greenwich Rhode Island 02818 —
Benchmark Research Austin Texas 78705 —
Texas Center for Drug Development, Inc. Houston Texas 77081 —
DM Clinical Research Tomball Texas 77375 —
J. Lewis Research, Inc. / Foothill Family Clinic Salt Lake City Utah 84109 —
J. Lewis Research, Inc. / Foothill Family Clinic South Salt Lake City Utah 84121 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05096208, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 12, 2023 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05096208 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →