New pneumonia vaccine passes first safety check in small study
NCT ID NCT06611033
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This early-stage study tested a new vaccine called V118 Formulation C in 65 healthy adults to see if it is safe and well-tolerated. Participants received either the new vaccine, an existing pneumonia vaccine (Prevnar 20), or a placebo. Researchers monitored for side effects like injection-site reactions and general symptoms. The study is complete, but results are not yet publicly available.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- V118 Formulation C (pneumococcal vaccine candidate)
- What this could lead to
- If successful, this could lead to a new vaccine option to help prevent pneumococcal disease.
- What could go wrong
- This is an early Phase 1 trial with only 65 healthy adults, so it is too soon to know if the vaccine will be effective or safe for larger populations.
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
-
Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
-
65 people
The number who actually took part.
- Started
-
Sep 2024
- Finished
-
Jan 2026
- Lead sponsor
-
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
-
18 to 49 years
- Sex
-
Anyone
- Healthy volunteers
-
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.
The main inclusion criteria include but are not limited to the following: * Is in good health before randomization Exclusion Criteria: * Has a history of invasive pneumococcal disease or known history of other culture-positive pneumococcal disease within 3 years prior to receiving study vaccination. * Has a history of clinically significant endocrine, GI, cardiovascular, hematological, hepatic, immunological, renal, respiratory, genitourinary, or major neurological (including stroke and chronic seizures) abnormalities or diseases.
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Genom att skicka in godkänner du våra Användarvillkor
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Research Centers of America ( Hollywood ) ( Site 0002)
Hollywood, Florida, 33024, United States
-
University of Texas Medical Branch ( Site 0001)
Galveston, Texas, 77555-1115, United States
-
Velocity Clinical Research, Hallandale Beach ( Site 0003)
Hallandale, Florida, 33009, United States
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