RecruitingPhase 3NCT07573462

A Study to Learn About the Safety of an Expanded Pneumococcal Vaccine in Healthy Infants

A PHASE 3, RANDOMIZED, DOUBLE-BLINDED TRIAL TO EVALUATE THE SAFETY AND TOLERABILITY OF A MULTIVALENT PNEUMOCOCCAL CONJUGATE VACCINE IN HEALTHY INFANTS


Sponsor

Pfizer

Enrollment

2,400 participants

Start Date

May 4, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to learn about the safety of a new pneumococcal vaccine and how the new pneumococcal vaccine helps to fight against germs that can cause pneumonia (lung infections), meningitis (brain infections), and otitis media (ear infections) in infants when compared to the pneumococcal vaccine that is currently in use, 20vPnC (Prevnar 20®). This study will test if the new pneumococcal vaccine is as safe as the one that is currently in use. This new vaccine can possibly provide additional protection against germs that cause pneumococcal disease that are not included in the vaccines that are currently given to infants. Pneumococcal disease includes a variety of infections caused by a specific germ, Streptococcus pneumoniae. There are two groups in this study. All participants will be assigned to one of the two groups. This study is seeking participants who are: \- infants who are about 2 months of age About 2400 infants will be assigned by chance to one of the two groups to receive either PG4 (new vaccine) or 20vPnC (currently in use) into the left thigh muscle at 2, 4, 6, and 12 to 15 months of age. Infants will take part in this study for about 16 to 19 months (about 1 and a half years). During this time, infants will have 6 study clinic visits and 1 phone call. At these study clinic visits, parent(s)/legal guardian(s) will be asked if the infant experienced any side effects. A side effect is an unintentional or unexpected reaction to a vaccine.


Eligibility

Min Age: 42 DaysMax Age: 98 Days

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a biological treatment called 20-valent pneumococcal conjugate vaccine (20vPnC) and a biological treatment called PG4 for people with pneumococcal disease. The study is currently recruiting participants at 21 locations.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BIOLOGICALPG4

Multivalent Pneumococcal Vaccine

BIOLOGICAL20-valent pneumococcal conjugate vaccine (20vPnC)

20-valent pneumococcal conjugate vaccine (20vPnC)


Locations(41)

Starz Pediatrics

Estero, Florida, United States

Innovate Research Centers, LLC

Fort Lauderdale, Florida, United States

MacKoul Pediatrics Fort Myers

Fort Myers, Florida, United States

Dr. Gala, LLC

Miami, Florida, United States

Rophe Adult and Pediatric Medicine/SKYCRNG

Union City, Georgia, United States

Rosemark Women Care Specialists

Idaho Falls, Idaho, United States

Eagle Clinical Research

Chicago, Illinois, United States

Kentucky Pediatric/ Adult Research

Bardstown, Kentucky, United States

LSU Health Shreveport Clinical Trials Office

Shreveport, Louisiana, United States

Ochsner/LSU Health Shreveport - Progressive Pediatrics

Shreveport, Louisiana, United States

Ochsner LSU Health Shreveport Ambulatory Care Center

Shreveport, Louisiana, United States

Ochsner/LSU Health Shreveport Academic Medical Center

Shreveport, Louisiana, United States

Pediatric Associates of Fall River

Fall River, Massachusetts, United States

Boston Children's Health Physicians

Hawthorne, New York, United States

Maria Fareri Children's Hospital

Valhalla, New York, United States

Senders Pediatrics

South Euclid, Ohio, United States

Legacy Clinical Trials

Oklahoma City, Oklahoma, United States

Cyn3rgy Research Corporation

Gresham, Oregon, United States

Donald Guthrie Foundation

Sayre, Pennsylvania, United States

Guthrie Medical Group

Sayre, Pennsylvania, United States

Tribe Clinical Research LLC. at Parkside Pediatrics Five Forks

Simpsonville, South Carolina, United States

National Research Centers, Plano LLC

Plano, Texas, United States

Pediatric Research of Charlottesville, LLC.

Gordonsville, Virginia, United States

The Children's Hospital at Westmead

Westmead, New South Wales, Australia

Queensland Children's Hospital

Brisbane, Queensland, Australia

Centre for Children's Health Research

South Brisbane, Queensland, Australia

Monash Health

Clayton, Victoria, Australia

Murdoch Children's Research Institute

Parkville, Victoria, Australia

Perth Children's Hospital

Nedlands, Western Australia, Australia

The Kids Research Institute Australia

Nedlands, Western Australia, Australia

Milestone Research Inc.

London, Ontario, Canada

Bluewater Clinical Research Group Inc.

Sarnia, Ontario, Canada

FVR, Kokkolan rokotetutkimusklinikka

Kokkola, Keski-Pohjanmaa, Finland

FVR, Oulun rokotetutkimusklinikka

Oulu, North Ostrobothnia, Finland

FVR, Tampereen rokotetutkimusklinikka

Tampere, Pirkanmaa, Finland

FVR, Espoon rokotetutkimusklinikka

Espoo, Uusimaa, Finland

FVR, Etelä-Helsingin rokotetutkimusklinikka

Helsinki, Uusimaa, Finland

MeVac - Meilahti Vaccine Research Center

Helsinki, Uusimaa, Finland

FVR, Järvenpään rokotetutkimusklinikka

Jarvenpaa, Uusimaa, Finland

Kinder- und Jugendarztpraxis Dr. med. Michael Horn

Schönau am Königssee, Bavaria, Germany

SZPZOZ im. Dzieci Warszawy w Dziekanowie Lesnym

Dziekanów Leśny, Poland

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NCT07573462


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