drugset / Trial / NCT04210752

Study to Assess the Safety, Tolerability and Explore the Immunogenicity of EG-HZ in Healthy Adult Volunteers

NCT04210752

RandomizedParallel-groupDouble-blindTreatment

Summary

This is a Phase 1, first in human (FIH), randomised, active-controlled, double-blind study designed to assess the safety and tolerability and explore preliminary efficacy of the EG-HZ vaccine. Oversight will be provided by a Safety Review Committee (SRC).

Timeline

Start
2020-02-24
Primary completion
2020-12-03
Completion
2020-12-03

Drugs

EvaluationDrugModalityDoseRoute
Subject EG-HZ-001 Unknown Intramuscular
Subject EG-HZ-002 Unknown Intramuscular
Subject EG-HZ-003 Unknown Intramuscular
Subject EG-HZ-004 Unknown Intramuscular
Subject VARICELLA ZOSTER VIRUS ENVELOPE GLYCOPROTEIN E Vaccine 0.5 ml Intramuscular

Indications