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Completed Phase 1Phase 2 Interventional Accepts healthy volunteers

A Study to Learn About the Safety and Immune Response of a New Pneumococcal Vaccine in Adults

ClinicalTrials.gov ID: NCT06182124

Public ClinicalTrials.gov record NCT06182124. 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, 6:11 PM 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 1/2, RANDOMIZED, DOUBLE-BLIND TRIAL OF THE SAFETY AND IMMUNOGENICITY OF A MULTIVALENT PNEUMOCOCCAL CONJUGATE VACCINE IN ADULTS 18 YEARS OF AGE AND OLDER

Brief summary

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

The purpose of this study is to learn about the safety and immune effects of a pneumococcal vaccine in adults. This vaccine can possibly provide protection against further pneumococcal disease. This study will happen in 4 stages: Stage 1 is seeking participants who are between 18 years to 49 years of age. The participants will receive 1 of 2 pneumococcal vaccine candidates (different formulations) or 20vPnC (Prevnar 20) as a single shot given into the upper arm muscle. Stage 2 will begin after participants have completed Stage 1, and a pneumococcal vaccine candidate has been decided. Stage 2 is seeking participants who are adults 50 years of age and older. The participants will receive the chosen pneumococcal vaccine candidate from Stage 1 or 20vPnC (Prevnar 20). The vaccines will be given as a single shot into the upper arm muscle. Stage 3 is seeking participants who are adults 50 years of age and older. The participants will receive the chosen pneumococcal vaccine candidate from Stage 1 or a licensed pneumococcal comparator vaccine. The vaccines will be given as a single shot into the upper arm muscle. Stage 4 is seeking participants who are adults 50 years of age and older. The participants will receive either one of three pneumococcal vaccine candidates or one of two licensed pneumococcal comparator vaccines. The vaccines will be given as a single shot into the upper arm muscle. Participants will take part in this study for about 6 months for Stage 1, Stage 3, and Stage 4 and 12 months for Stage 2. During this time participants will have from 2 to 4 clinic visits and 1 phone visit. At these clinic visits, participants will be asked if any side effects were experienced. The participants will also have to give blood samples during these clinic visits.

Study identification

NCT ID
NCT06182124
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
1,710 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 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
Dec 20, 2023 (Actual)
Primary completion
May 12, 2026 (Actual)
Completion
May 12, 2026 (Actual)
Last update posted
Sep 25, 2026

2023 – 2026

United States locations

U.S. sites
20
U.S. states
10
U.S. cities
16
Facility City State ZIP Site status
Alliance for Multispecialty Research, LLC Doral Florida 33172 —
Indago Research & Health Center, Inc Hialeah Florida 33012 —
Clinical Research Atlanta Stockbridge Georgia 30281 —
Optimal Research Peoria Illinois 61614 —
Alliance for Multispecialty Research, LLC New Orleans Louisiana 70119 —
Headlands Research - Detroit Southfield Michigan 48034 —
Rochester Clinical Research, LLC Rochester New York 14609 —
IMA Evaluations, LLC dba IMA Clinical Research Tarrytown New York 10591 —
Accellacare - Wilmington Wilmington North Carolina 28401 —
AMR Clinical Knoxville Tennessee 37909 —
AMR Clinical Knoxville Tennessee 37920 —
Headlands Horizons LLC Brownsville Texas 78526 —
DM Clinical Research- Cyfair Houston Texas 77065 —
Clinical Trials of Texas, LLC dba Flourish Research San Antonio Texas 78229 —
IMA Clinical Research San Antonio San Antonio Texas 78229 —
Dynamed Clinical Research, LP d/b/a DM Clinical Research Sugarland Texas 77478 —
DM Clinical Research Tomball Texas 77375 —
Dynamed Clinical Research, LP d/b/a DM Clinical Research Tomball Texas 77375 —
J. Lewis Research, Inc. / Foothill Family Clinic Salt Lake City Utah 84109 —
J. Lewis Research, Inc. Salt Lake City Utah 84109 —

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 NCT06182124, 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 Sep 25, 2026 · 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 NCT06182124 live on ClinicalTrials.gov.

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