drugset / Trial / NCT06961721

A Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase IV Clinical Trial to Evaluate the Immunogenicity and Safety of a Live Attenuated Herpes Zoster Vaccine in Adults Aged 40 Years and Older

NCT06961721 ↗

RandomizedParallel-groupQuadruple-blindPrevention

Summary

To evaluate the immunogenicity 42 days after vaccination with the live attenuated herpes zoster vaccine. To evaluate the safety of the live attenuated herpes zoster vaccine.

Timeline

Start
2025-05
Primary completion
2025-07
Completion
2025-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Herpes Zoster Vaccine, Live Vaccine 0.5 ml —

Indications