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Completed Phase 2 Interventional Accepts healthy volunteers Results available

A Study to Learn About Two or More Vaccines That Are Put Together as One Shot Against Infectious Lung Illnesses, Including COVID-19 and Respiratory Syncytial Virus (RSV).

ClinicalTrials.gov ID: NCT05886777

Public ClinicalTrials.gov record NCT05886777. 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 23, 2026, 2:04 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 STUDY TO EVALUATE THE SAFETY, TOLERABILITY, AND IMMUNOGENICITY OF COMBINED VACCINE CANDIDATE(S) AGAINST INFECTIOUS RESPIRATORY ILLNESSES, INCLUDING COVID-19 AND RSV, IN HEALTHY INDIVIDUALS

Brief summary

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

The purpose of the study is to learn about the safety and effects of a combined vaccine for RSV and COVID-19 when given with a seasonal flu vaccine or when given alone. A combined vaccine will help to reduce the number of vaccinations given when trying to prevent respiratory infections. This study is seeking participants who: * are 65 years of age or older. * are healthy or have well-controlled chronic conditions. * in the past have received at least 3 US-authorized mRNA COVID 19 vaccines, with the most recent vaccine being an updated booster vaccine given at least more than or equal to 150 days before Visit A101 (Day 1). * have not had a flu shot in the last 120 days. * agree to be present for all study visits, procedures, and blood draws. Participants will be involved in this study for 6 months. During this time, participants will have 2 study visits at the study clinic and a 6-month telephone contact.

Study identification

NCT ID
NCT05886777
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
1,142 participants

Conditions and interventions

Eligibility (public fields only)

Age range
65 Years and older
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
Jun 5, 2023 (Actual)
Primary completion
Jan 1, 2024 (Actual)
Completion
Jan 1, 2024 (Actual)
Last update posted
Dec 18, 2024

2023 – 2024

United States locations

U.S. sites
37
U.S. states
14
U.S. cities
29
Facility City State ZIP Site status
West Coast Research Dublin California 94568 —
Marvel Clinical Research Huntington Beach California 92647 —
Orange County Research Center Lake Forest California 92630 —
Artemis Institute for Clinical Research San Diego California 92103 —
California Research Foundation San Diego California 92123 —
Orange County Research Center Tustin California 92780 —
Diablo Clinical Research, Inc. Walnut Creek California 94598 —
Clinical Research Consulting Milford Connecticut 06460 —
Indago Research & Health Center, Inc Hialeah Florida 33012 —
Wr-Msra.Llc Lake City Florida 32055 —
Optimal Research Melbourne Florida 32934 —
Suncoast Research Group Miami Florida 33135 —
Clinical Site Partners, LLC dba CSP Orlando Winter Park Florida 32789 —
Clinical Site Partners, LLC dba Flourish Research Winter Park Florida 32789 —
Great Lakes Clinical Trials - Gurnee Gurnee Illinois 60031 —
Optimal Research Peoria Illinois 61614 —
Bio-Kinetic Clinical Applications LLC DBA QPS_MO (Patient Screening Only) Springfield Missouri 65802 —
Bio-Kinetic Clinical Applications, LLC dba QPS-MO Springfield Missouri 65802 —
Bio-Kinetic Clinical Applications, LLD dba QPS-MO Springfield Missouri 65802 —
Las Vegas Clinical Trials Las Vegas Nevada 89030 —
Las Vegas Clinical Trials North Las Vegas Nevada 89030 —
Drug Trials America Hartsdale New York 10530 —
Accellacare - Wilmington - 1917 Tradd Court Wilmington North Carolina 28401 —
Accellacare - Wilmington Wilmington North Carolina 28401 —
Centricity Research Columbus Ohio Multispecialty Columbus Ohio 43213 —
Coastal Carolina Research Center North Charleston South Carolina 29405 —
Clinical Research Associates Inc Nashville Tennessee 37203 —
Headlands Horizons LLC Brownsville Texas 78526 —
DM Clinical Research - Cy Fair Houston Texas 77065 —
DM Clinical Research- Cyfair Houston Texas 77065 —
DM Clinical Research - Bellaire Houston Texas 77081 —
SMS Clinical Research Mesquite Texas 75149 —
Clinical Trials of Texas, LLC San Antonio Texas 78229 —
DM Clinical Research, Martin Diagnostic Clinic 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 —
Virginia Research Center Midlothian Virginia 23114 —

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 NCT05886777, 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 Dec 18, 2024 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05886777 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →