drugset / Trial / NCT01827839

Immunogenicity and Safety of GlaxoSmithKline (GSK) Biologicals' Herpes Zoster Subunit (HZ/su) Vaccine GSK1437173A in Adults With a Prior Episode of Herpes Zoster

NCT01827839 ↗

Phase 3 Completed 96 enrolled GlaxoSmithKline
NaSingle-groupOpen-labelPrevention

Summary

The purpose of this study is to evaluate the immunogenicity and safety of GSK Biologicals' HZ/su vaccine in subjects' ≥ 50 years of age (YOA) who previously have had Herpes Zoster (HZ). The data collected will be compared with the data from subjects without HZ in other HZ/su trials.

Timeline

Start
2013-06-10
Primary completion
2014-02-10
Completion
2014-11-25

Outcome

Met primary endpoint

paper The primary immunogenicity objective was met, as the VRR at Month 3 was 90.2% (95% CI: 81.7-95.7). PMID 28068212 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Shingrix Vaccine — Intramuscular

Indications