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NCT05634811

PHASE3

Safety Study of a Vaccine to Help Protect Against Lyme Disease in Healthy Children

Sponsor: Pfizer

View on ClinicalTrials.gov

Summary

This study is to understand if the study vaccine (called VLA15) is safe in healthy children. We are looking for children who: * are healthy * are age 5 through 17 * have not been diagnosed with any form of Lyme disease in the past * have not received any vaccines for Lyme disease in the past Lyme disease happens most often in children of this age. The study vaccine may be used potentially to help prevent Lyme disease. The goal of this study is to get more information about the safety of the study vaccine in this age group. Participants will be in this study for about 2 years. During that time, they will receive VLA15 or placebo (sterile saltwater solution) by a "shot" in the arm. We will compare experience of children receiving VLA15 to those receiving the placebo. Participants will not know whether they get VLA15 or placebo. Everyone participating in this study will: * get the shots in a clinic or in a hospital office * receive a total of 4 shots * receive the first 3 shots within 6 months * receive the last shot about 1 year afterwards * need to come to the trial site for 6 planned visits; 4 of these are vaccination visits and 2 are follow-up visits. We will contact you by phone 1 time every year during the study to monitor your experience. You may have extra visits if you experience a severe reaction after a vaccine dose.

Official title: A PHASE 3, RANDOMIZED, PLACEBO-CONTROLLED, OBSERVER-BLINDED TRIAL TO EVALUATE THE SAFETY OF A 6-VALENT OspA-BASED LYME DISEASE VACCINE (VLA15) IN HEALTHY CHILDREN 5 THROUGH 17 YEARS OF AGE

Key Details

Gender

All

Age Range

5 Years - 17 Years

Study Type

INTERVENTIONAL

Enrollment

3547

Start Date

2022-12-12

Completion Date

2025-07-21

Last Updated

2026-05-07

Healthy Volunteers

Yes

Conditions

Lyme Disease

Interventions

BIOLOGICAL

VLA15

6-valent OspA-based Lyme disease vaccine

OTHER

Normal Saline

0.9% sodium chloride solution for injection

Inclusion Criteria: * Healthy participants at enrollment who are determined to be eligible for inclusion in the study. Participants with preexisting chronic medical conditions determined to be stable may be included. * Participants and/or participants' parent(s)/guardian who are willing and able to comply with all scheduled visits, study procedures and lifestyle considerations for the duration of the study. Exclusion Criteria: * Female participants that are pregnant, breastfeeding, or have a positive urine pregnancy test at Visit 1. Sexually active females and fertile males unwilling to use contraception as per protocol. * Any contraindication to vaccination or vaccine components, including previous anaphylactic reaction to any vaccine or vaccine-related components. * Any diagnosis of Lyme disease within the past 3 months. * Any history of Lyme arthritis, carditis, neuroborreliosis, or other disseminated Lyme Disease (LD), regardless of when diagnosed. * Known tick bite within the past 4 weeks. * Congenital or acquired immunodeficiency or other conditions or treatments associated with immunosuppression that would inhibit the ability to mount an immune response to a vaccine. * Other medical, psychiatric condition, active suicidal ideation/behavior or lab abnormality which increases risk of study participation or, in investigator's judgment is inappropriate for the study. * Receipt of a previous vaccination for LD. * Treatment for LD in the 3 months prior to study intervention administration. * Receipt of blood/plasma products or immunoglobulins within 6 months before study intervention administration through conclusion of the study. * Receipt of systemic corticosteroids for ≥14 days within 28 days before study intervention administration. Inhaled/nebulized, intra-articular, intrabursal, or topical corticosteroids are permitted. * Receipt of chronic systemic treatment with other known immunosuppressant medications, or radiotherapy, within 6 months before study intervention administration. * Current use of any prohibited concomitant medication(s) or participants unwilling/unable to use a permitted concomitant medication(s). * Participation in other studies involving investigational drugs/vaccines/devices within 28 days prior to study entry and/or during study participation (observational studies are acceptable). * Investigator site staff, sponsor/sponsor delegates directly involved in the conduct of the study and their family members; site staff supervised by the investigator and their family members.

Locations (65)

UAB Child Health Research Unit (CHRU)

Birmingham, Alabama, United States

University of Alabama at Birmingham - School of Medicine

Birmingham, Alabama, United States

Lakeview Clinical Research

Guntersville, Alabama, United States

Coast Clinical Research, LLC

Bellflower, California, United States

Apex Research Group LLC

Fair Oaks, California, United States

New England Research Associates

Bridgeport, Connecticut, United States

Stamford Therapeutics Consortium

Stamford, Connecticut, United States

Children's National Medical Center

Washington D.C., District of Columbia, United States

Bio-Medical Research LLC

Miami, Florida, United States

GCP Research, Global Clinical professionals

St. Petersburg, Florida, United States

MOORE Clinical Research, Inc. d/b/a TrueBlue Clinical Research

Tampa, Florida, United States

ForCare Clinical Research

Tampa, Florida, United States

Tekton Research, LLC.

Chamblee, Georgia, United States

ASR, LLC

Boise, Idaho, United States

Clinical Research Prime

Idaho Falls, Idaho, United States

Clinical Research Prime Rexburg

Rexburg, Idaho, United States

University of Chicago Medical Center

Chicago, Illinois, United States

AMR Clinical

El Dorado, Kansas, United States

AMR Clinical

Wichita, Kansas, United States

Kentucky Pediatric/ Adult Research

Bardstown, Kentucky, United States

All Children Pediatrics

Louisville, Kentucky, United States

MD Medical Research

Oxon Hill, Maryland, United States

White Oak Pediatrics

Silver Spring, Maryland, United States

Sisu BHR

Springfield, Massachusetts, United States

Michigan Center of Medical Research (MICHMER)

Bingham Farms, Michigan, United States

Vida Clinical Studies, LLC

Dearborn Heights, Michigan, United States

Great Lakes Research Institute

Southfield, Michigan, United States

Clinical Research Institute

Minneapolis, Minnesota, United States

Velocity Clinical Research, Omaha

Omaha, Nebraska, United States

Hassman Research Institute

Marlton, New Jersey, United States

Rutgers University

New Brunswick, New Jersey, United States

IMA Clinical Research Warren

Warren Township, New Jersey, United States

Velocity Clinical Research, Binghamton

Binghamton, New York, United States

Buffalo Clinical and Translational Research Center

Buffalo, New York, United States

Advanced Specialty Care

Commack, New York, United States

Smith Allergy and Asthma Specialists

Cortland, New York, United States

Stony Brook Medicine Clinical Research Center

East Setauket, New York, United States

Upstate Global Health Institute

East Syracuse, New York, United States

Southampton Hospital

Hampton Bays, New York, United States

Smith Allergy & Asthma Specialists

Horseheads, New York, United States

NYU Langone Hospital - Long Island

Mineola, New York, United States

DiGiovanna Institute for Medical Education & Research

North Massapequa, New York, United States

Rochester Clinical Research, LLC

Rochester, New York, United States

Stony Brook University

Stony Brook, New York, United States

Prime Global Research

The Bronx, New York, United States

Advantage Clinical Trials

The Bronx, New York, United States

Velocity Clinical Research, Vestal

Vestal, New York, United States

Centricity Research Columbus Ohio Multispecialty

Columbus, Ohio, United States

Allegheny Health and Wellness Pavilion

Erie, Pennsylvania, United States

Central Erie Primary Care

Erie, Pennsylvania, United States

Preferred Primary Care Physicians, Preferred Clinical Research (Ofc 18)

Pittsburgh, Pennsylvania, United States

Northeast Clinical Trials Group

Scranton, Pennsylvania, United States

Coastal Carolina Research Center

North Charleston, South Carolina, United States

Benchmark Research

Austin, Texas, United States

Benchmark Research

Fort Worth, Texas, United States

Texas Health Resources

Fort Worth, Texas, United States

C & R Research Services USA

Houston, Texas, United States

DM Clinical Research - Kool Kids Pediatrics

Houston, Texas, United States

Research Your Health

Plano, Texas, United States

Sun Research Institute

San Antonio, Texas, United States

Velocity Clinical Research, Salt Lake City

West Jordan, Utah, United States

Pediatric Research of Charlottesville, LLC

Charlottesville, Virginia, United States

Clinical Research Partners, LLC

Richmond, Virginia, United States

Frontier Clinical research

Kingwood, West Virginia, United States

Preston Healthcare Services