drugset / Trial / NCT05496231

A Study on the Immune Response and Safety of an Adjuvanted Human Papillomavirus Vaccine When Given to Healthy Women 16 to 26 Years of Age

NCT05496231

Phase 1/2 Completed 1080 enrolled GlaxoSmithKline
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The main purpose of this study was to evaluate the safety and reactogenicity of GlaxoSmithKline Biologicals SA (GSK)'s investigational adjuvanted human papillomavirus (HPV) vaccine formulations.

Timeline

Start
2022-08-22
Primary completion
2024-02-23
Completion
2024-02-25

Drugs

EvaluationDrugModalityDoseRoute
Comparator Gardasil 9 Vaccine Intramuscular
Subject HPV9 Vaccine Intramuscular