One vaccine to fight five types of meningitis? pfizer tests new combo shot in teens
NCT ID NCT04440176
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This Pfizer study tested a new 5-in-1 vaccine (MenABCWY) that targets five types of meningococcal bacteria, which can cause serious infections like meningitis. The trial involved 309 healthy teens aged 11 to 14 and compared two different dosing schedules (shots 12 months apart vs. 36 months apart). Researchers measured how well the vaccine triggered an immune response and tracked any side effects. The goal is to find a safe and effective way to protect adolescents with fewer shots.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- pentavalent meningococcal vaccine (MenABCWY)
- What this could lead to
- If successful, this could lead to a simpler vaccination schedule that protects against five types of meningococcal disease with fewer shots.
- What could go wrong
- This is a Phase 2b trial with only 309 participants, so results may not apply to everyone. The vaccine may not provide long-lasting protection or could have side effects not seen in this small study.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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309 people
The number who actually took part.
- Started
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Jun 2020
- Finished
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Jan 2024
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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11 to 14 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Male or female participants 11 through \<15 years of age at the time of randomization. * Participants who have never received a prior dose of any meningococcal vaccine. Written confirmation of vaccination history must be obtained prior to randomization. * Available for the entire study period and can be reached by telephone. * Healthy participant as determined by medical history, physical examination, and judgement of the investigator. * Negative urine pregnancy test for all female participants; pregnancy test is not applicable to male participants. Exclusion Criteria: * A previous anaphylactic reaction to any vaccine or vaccine-related component. * Bleeding diathesis or condition associated with prolonged bleeding time that would contraindicate intramuscular injection. * A known or suspected defect of the immune system that would prevent an immune response to the vaccine, such as participants with congenital or acquired defects in B-cell function, those receiving chronic systemic (oral, intravenous, or intramuscular) corticosteroid therapy, or those receiving immunosuppressive therapy. * History of microbiologically proven disease caused by Neisseria meningitidis or Neisseria gonorrhoeae. * Significant neurological disorder or history of seizure (excluding simple febrile seizure). * Any neuroinflammatory or autoimmune condition, including, but no limited to, transverse myelitis, uveitis, optic neuritis, and multiple sclerosis. * Participants receiving any allergen immunotherapy with a nonlicensed product or receiving allergen immunotherapy with a licensed product and are not on stable maintenance doses. * Receipt of any blood products, including immunoglobulin, within 6 months before the first study vaccination. * Current use of systemic antibiotics with no foreseeable date of discontinuation prior to anticipated date of enrollment (first vaccination).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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AMR Clinical
Mobile, Alabama, 36608, United States
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AMR Clinical
Roy, Utah, 84067, United States
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AMR Clinical
South Jordan, Utah, 84095, United States
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Benchmark Research
Fort Worth, Texas, 76135, United States
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California Research Foundation
San Diego, California, 92123, United States
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Cincinnati Children's Hospital Medical Center
Cincinnati, Ohio, 45206, United States
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Cincinnati Children's Hospital Medical Center
Cincinnati, Ohio, 45229, United States
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Coastal Carolina Research Center
North Charleston, South Carolina, 29405, United States
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Diagnostics Research Group
San Antonio, Texas, 78229, United States
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J. Lewis Research, Inc. / Foothill Family Clinic
Salt Lake City, Utah, 84109, United States
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J. Lewis Research, Inc. / Foothill Family Clinic South
Salt Lake City, Utah, 84121, United States
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Nona Pediatric Center
Orlando, Florida, 32829, United States
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Ohio Pediatric Research Association Inc.
Dayton, Ohio, 45414, United States
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Pediatric Research of Charlottesville, LLC
Charlottesville, Virginia, 22902, United States
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Texas Health Resources
Fort Worth, Texas, 76135, United States
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Utah Valley Pediatrics - Timpanogos Office
Orem, Utah, 84057, United States
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Velocity Clinical Research, Norfolk
Norfolk, Nebraska, 68701, United States
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Wasatch Pediatrics, Cottonwood Office
Murray, Utah, 84107, United States
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Wee Care Pediatrics
Kaysville, Utah, 84037, United States
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Wee Care Pediatrics
Syracuse, Utah, 84075, United States