New flu vaccine shows promise for teens and adults
NCT ID NCT05513053
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tested a recombinant flu vaccine (RIV4) in over 1,300 people aged 9 to 49. The goal was to see if the immune response in children and teens (9-17) was as good as in adults (18-49). Researchers measured antibody levels before and 29 days after vaccination. The trial also monitored safety for all participants.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Quadrivalent recombinant influenza vaccine (RIV4), also known as Supemtek or Flublok Quadrivalent
- What this could lead to
- If successful, this could confirm that the recombinant flu vaccine works as well in teens as in adults, offering a safe option for younger age groups.
- What could go wrong
- This is a completed phase 3 trial, but results only show immune response and short-term safety. Long-term protection and real-world effectiveness are not yet proven.
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 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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1,308 people
The number who actually took part.
- Started
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Oct 2022
- Finished
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Oct 2023
- 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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9 to 49 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: * Aged 9 to 49 years on the day of inclusion * A female participant was eligible to participate if she was not pregnant or breastfeeding and one of the following conditions applies: 1) was of non-childbearing potential. To be considered of non-childbearing potential, a female should have been pre-menarche, post-menopausal for at least 1 year, or surgically sterile OR 2) was of childbearing potential and agreed to use an effective contraceptive method or abstinence from at least 4 weeks prior to the first study intervention administration until at least 4 weeks after the last study intervention administration * Assent form or informed consent form had been signed and dated by the participant (based on local regulations), and if applicable informed consent form had been signed and dated by the parent(s) or another legally acceptable representative Exclusion Criteria: * Known or suspected congenital or acquired immunodeficiency, or receipt of immunosuppressive therapy, such as anti-cancer chemotherapy or radiation therapy, within the preceding 6 months; or long-term systemic corticosteroid therapy (prednisone or equivalent for more than 2 consecutive weeks within the past 3 months) * Known systemic hypersensitivity to any of the vaccine components, or history of a life-threatening reaction to the vaccines used in the trial or to a vaccine containing any of the same substances * Thrombocytopenia * Bleeding disorder, or receipt of anticoagulants in the 3 weeks preceding inclusion, contraindicating intramuscular vaccination based on the Investigator's judgment * Personal or family history of Guillain-Barre Syndrome (GBS) * Personal history of clinically significant development delay (at the discretion of the Investigator), neurologic disorder, or seizure disorder NOTE: The above information was not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
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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 - Newton Site Number : 8400021
Newton, Kansas, 67114, United States
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Alabama Clinical Therapeutics North Tower Site Number : 8400024
Birmingham, Alabama, 35205, United States
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Benchmark Research - Austin Site Number : 8400004
Austin, Texas, 78705, United States
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Birmingham Pediatric Associates Site Number : 8400023
Birmingham, Alabama, 35205, United States
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California Research Foundation Site Number : 8400003
San Diego, California, 92123-1881, United States
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Coastal Carolina Research Center - N Charleston Site Number : 8400022
North Charleston, South Carolina, 29405, United States
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Coastal Pediatric Research Charleston Site Number : 8400005
Charleston, South Carolina, 29414, United States
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Investigational Site Number : 2030001
Jindřichův Hradec, 37701, Czechia
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Investigational Site Number : 6160003
Bydgoszcz, 85-796, Poland
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Investigational Site Number : 6160004
PuÅ'awy, Lubusz Voivodeship, 24-100, Poland
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Investigational Site Number : 6160005
Siemianowice Śląskie, Silesian Voivodeship, 41-103, Poland
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Investigational Site Number : 6160006
Tarnów, 33-100, Poland
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Investigational Site Number : 6160007
Bydgoszcz, Kuyavian-Pomeranian Voivodeship, 85-079, Poland
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Investigational Site Number : 6160008
Warsaw, 02-637, Poland
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Investigational Site Number : 6160010
Bydgoszcz, Kuyavian-Pomeranian Voivodeship, 85-048, Poland
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Investigational Site Number : 6160012
Wroclaw, 53-149, Poland
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Investigational Site Number : 7240001
Móstoles, 28938, Spain
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Investigational Site Number : 7240005
Málaga, 29015, Spain
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Investigational Site Number : 7240006
Centelles, Barcelona [Barcelona], 08540, Spain
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Investigational Site Number : 7240007
Seville, 41014, Spain
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Investigational Site Number : 7240018
Madrid, 28660, Spain
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J. Lewis Research Site Number : 8400017
Salt Lake City, Utah, 84109, United States
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JBR Clinical Research Site Number : 8400001
Salt Lake City, Utah, 84107, United States
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Kentucky Pediatics / Adult Research Site Number : 8400010
Bardstown, Kentucky, 40004, United States
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Meridian Clinical Research Norfolk Site Number : 8400011
Norfolk, Nebraska, 68701, United States
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Meridian Clinical Research Site Number : 8400006
Binghamton, New York, 13905, United States
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Meridian Clinical Research- Sioux City Site Number : 8400007
Sioux City, Iowa, 51106, United States
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Ohio Pediatric Research Site Number : 8400020
Dayton, Ohio, 45414, United States
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Rainbow Pediatrics Site Number : 8400014
Barnwell, South Carolina, 29812, United States
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The Children's Clinic Of Jonesboro PA Site Number : 8400025
Jonesboro, Arkansas, 72401, United States
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Velocity Clinical Research Lincoln Site Number : 8400013
Lincoln, Nebraska, 68510, United States
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Velocity Clinical Research Portsmouth Site Number : 8400015
Portsmouth, Virginia, 23703, United States
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Velocity Clinical Research Site Number : 8400012
New Orleans, Louisiana, 70119, United States
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Velocity Clinical Research Vestal Site Number : 8400016
Vestal, New York, 13850, United States
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Velocity Clinical Research, Omaha Site Number : 8400009
Omaha, Nebraska, 68134, United States
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Other studies related to the condition(s) this trial covers.
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