drugset / Trial / NCT07105722

A Trial to Evaluate the Safety and Immune Response of an Investigational Pneumococcal Vaccine in Adults 50 To 64 Years of Age

NCT07105722

Phase 1 Completed 127 enrolled GlaxoSmithKline
RandomizedParallel-groupTriple-blindPrevention

Summary

This clinical study is designed to evaluate an investigational pneumococcal vaccine named Pn-MAPS30plus. The vaccine is designed to stimulate the immune system to produce antibodies against various serotypes of the S. pneumoniae bacteria, potentially aiding the body in fighting infection upon exposure. Pn-MAPS30plus aims to broaden protection by covering more serotypes than currently licensed pneumococcal vaccines. The study's purpose is to determine whether the vaccine is safe, well-tolerated, and effective in inducing immune responses against S. pneumoniae.

Timeline

Start
2025-08-12
Primary completion
2026-05-06
Completion
2026-05-06

Drugs

EvaluationDrugModalityDoseRoute
Subject PCV20 Vaccine Intramuscular
Subject Pn-MAPS30plus Vaccine Intramuscular

Indications