drugset / Trial / NCT07406334
A Trial to Evaluate the Safety and Reactogenicity of an Investigational Pneumococcal Vaccine in Toddlers 12 to 15 Months of Age Receiving a Single Booster Dose
RandomizedParallel-groupTriple-blindPrevention
Summary
The main purpose of this study is to assess the safety and reactogenicity of a single dose of the new pneumococcal vaccine (called Pn-MAPS30plus) in toddlers who have previously completed a two-dose primary vaccination series with PCV used in local immunization program. PCV20 will be used as a comparator for this study.
Timeline
- Start
- 2026-05-15
- Primary completion
- 2027-02-22
- Completion
- 2027-02-22
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | PCV20 | Vaccine | — | Intramuscular |
| Subject | Pn-MAPS30plus | Vaccine | — | Intramuscular |