drugset / Trial / NCT01165229

Study to Evaluate Efficacy, Safety and Immunogenicity of GlaxoSmithKline (GSK) Biologicals' Herpes Zoster (HZ) Vaccine GSK1437173A in Adults Aged 70 Years and Older

NCT01165229 ↗

Phase 3 Completed 14819 enrolled GlaxoSmithKline
RandomizedParallel-groupTriple-blindPrevention

Summary

The purpose of this observer-blind study is to evaluate the efficacy, safety and immunogenicity of GSK Biologicals' candidate Herpes Zoster (HZ) vaccine in adults aged ≥ 70 years. Two studies (Zoster-006 \[NCT01165177\] and Zoster-022 \[NCT01165229\]) will be conducted concurrently to evaluate efficacy of GSK1437173A vaccine. A pooled analysis of data from both studies combined will be conducted contingent on each study achieving its objectives. This protocol posting also deals with the outcome measures related to the pooled analysis.

Timeline

Start
2010-08-02
Primary completion
2015-07-24
Completion
2015-07-24

Outcome

Met primary endpoint

registry Zoster-022 GSK1437173A >=70YOA Group vs Zoster-022 Placebo >=70YOA Group; p <0.0001; Vaccine efficacy 89.79 NCT01165229 ↗

registry Zoster-022/006 Pooled GSK1437173A >=70YOA Group vs Zoster-022/006 Pooled Placebo >=70YOA Group; p <0.0001; Vaccine efficacy 88.78 NCT01165229 ↗

registry Zoster-022/006 Pooled GSK1437173A >=70YOA Group vs Zoster-022/006 Pooled Placebo >=70YOA Group; p <0.0001; Vaccine efficacy 91.30 NCT01165229 ↗

release “ZOE-70) successfully met its primary objective, demonstrating 90% (95% confidence interval: 84–94) efficacy against shingles compared to placebo.” gsk.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Shingrix Vaccine — Intramuscular

Indications