drugset / Trial / NCT01610414

Study to Evaluate Efficacy, Safety, and Immunogenicity of GlaxoSmithKline (GSK) Biologicals' Herpes Zoster Vaccine GSK1437173A

NCT01610414 ↗

Phase 3 Completed 1877 enrolled GlaxoSmithKline
RandomizedParallel-groupTriple-blindPrevention

Summary

The purpose of this study is to evaluate the efficacy of GSK Biologicals' vaccine GSK1437173A in the prevention of Herpes zoster (HZ) in autologous haematopoietic cell transplant recipients 18 years of age and older. To this end, the study will evaluate vaccine efficacy (VE) of the GSK1437173A vaccine, administered on a 2-dose schedule, compared to placebo in reducing the risk of developing HZ in this population.

Timeline

Start
2012-07-13
Primary completion
2016-11-04
Completion
2017-02-01

Outcome

Met primary endpoint

registry analysis (superiority test); GSK1437173A Group vs Placebo Group; p <0.0001; Vaccine efficacy 68.17 (95% CI 55.56 to 77.53); Poisson method NCT01610414 ↗

paper During the 21-month median follow-up, at least 1 herpes zoster episode was confirmed in 49 vaccine and 135 placebo recipients PMID 31287523 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Shingrix Vaccine — Intramuscular

Indications