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

NCT07406334

Phase 1 Not yet recruiting 45 enrolled GlaxoSmithKline
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

EvaluationDrugModalityDoseRoute
Subject PCV20 Vaccine Intramuscular
Subject Pn-MAPS30plus Vaccine Intramuscular

Indications