How pneumococcal conjugate vaccines may produce antibodies that protect against serogroup 33.
Official title: Novel Serotype Alert: Investigate New Pneumococcal Conjugate Vaccines for Inducing Cross-protection Against Newly Discovered Serotype 33E and Putative Novel Serogroup 33 Serotypes
Run by University of Alabama at Birmingham · NCT07135453 · Data updated 2026-11-12
This will try two different pneumococcal conjugate vaccines in healthy adults to see which one makes antibodies that can kill serogroup 33 bacteria.
Quick facts
| Phase | Phase 4 |
|---|---|
| Study type | Interventional |
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 70 (estimated) |
| Sponsor | University of Alabama at Birmingham Academic / other |
| Locations | 1 site (Birmingham, Alabama) |
| Status | Recruiting |
| Started | July 1, 2026 |
| Main results expected | March 2027 |
| Study ends | August 2027 |
| Registry record updated | August 21, 2026 |
| Trial ID | NCT07135453 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Healthy adults with no prior pneumococcal vaccination and no chronic diseases or medications that suppress the immune system are ideal candidates.
✕Probably not a fit
People who are immunocompromised, have chronic immune-impacting conditions, or who have already received a pneumococcal vaccine are unlikely to qualify or benefit from this protocol.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
In this Phase 4, post-licensure comparison, healthy adult participants will receive one of two licensed pneumococcal conjugate vaccines and have blood drawn before and after vaccination. Laboratory assays will measure the presence and bactericidal activity of antibodies specifically against serogroup 33. Individuals with prior pneumococcal vaccination or conditions/medications that suppress immunity are excluded. The study is conducted at the University of Alabama at Birmingham in collaboration with Merck.
Why it matters
Potential benefit: If successful, the results could show that an existing pneumococcal conjugate vaccine provides cross-protection against serogroup 33 and guide vaccine choice or future vaccine design.
How similar studies have gone: Some prior work has shown pneumococcal conjugate vaccines can induce cross-reactive antibodies, but protection specifically against serogroup 33 remains uncertain.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Healthy adult Exclusion Criteria: * No prior history of pneumococcal vaccination * No immunosuppressing medications or chronic diseases that affect immune function
Where it's running
-
University of Alabama at Birmingham
Birmingham, Alabama, United States Recruiting
Study contacts
- Study coordinator: David LaFon, MD
- Email: dlafon@uabmc.edu
- Phone: 2059343411
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Safety and immune response of three PG4 vaccine lots vs 20vPnC in adults
This study tests three different lots of a new pneumococcal vaccine and the standard 20vPnC vaccine in adults to see if they are similarly safe and provoke a similar immune response.
-
New pneumococcal vaccine safety and immune response in children and teens
This study tests whether a new pneumococcal vaccine is as safe and as effective as Prevnar 20 in children and adolescents who have previously received PCV.
-
New pneumococcal vaccine in infants shows safety and how it stacks up against Prevnar 20
A new pneumococcal vaccine is being tested in healthy infants to see if it is as safe as Prevnar 20 and whether it triggers a similar or better immune response.
-
New pneumococcal vaccine for healthy infants
A new pneumococcal vaccine is being tested in about 2-month-old healthy babies to see if it is as safe as Prevnar 20 and whether it may offer broader protection against germs that cause pneumonia, meningitis, and ear infections.
-
Serum collection after Gamma-PN vaccination to support assay development
This project will collect blood samples from people who receive the Gamma-PN vaccine to help develop lab tests for pneumococcal disease.
-
Pneumococcal Vaccine Test for severely malnourished kids in hospital
This study tests whether giving Pneumosil to children aged 6–59 months with severe acute malnutrition in hospital elicits a better immune response than a Typhoid vaccine, with follow-up visits over six months.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.