drugset / Trial / NCT04210752
Study to Assess the Safety, Tolerability and Explore the Immunogenicity of EG-HZ in Healthy Adult Volunteers
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |