Trial to Evaluate the Safety, Tolerability, and Immunogenicity of an Investigational Herpes Zoster Vaccine (Z-1018) Compared to Shingrix® in Healthy Adult Volunteers

PHASE1CompletedINTERVENTIONAL
Enrollment

150

Participants

Timeline

Start Date

January 10, 2022

Primary Completion Date

October 20, 2022

Study Completion Date

October 20, 2022

Conditions
ShinglesHerpes ZosterVaccine-Preventable Diseases
Interventions
BIOLOGICAL

Z-1018

contains gE at a dose of 100 mcg to be combined with a Toll-like receptor 9 agonist adjuvant, CpG 1018 at dose of 3000 mcg

BIOLOGICAL

Z-1018

contains gE at a dose of 100 mcg to be combined with a Toll-like receptor 9 agonist adjuvant, CpG 1018 at dose of 3000 mcg with aluminum hydroxide (alum)

BIOLOGICAL

Z-1018

contains gE at a dose of 100 mcg to be combined with a Toll-like receptor 9 agonist adjuvant, CpG 1018 at dose of 6000 mcg

BIOLOGICAL

Z-1018

contains gE at a dose of 100 mcg to be combined with a Toll-like receptor 9 agonist adjuvant, CpG 1018 at dose of 6000 mcg, with aluminum hydroxide (alum)

BIOLOGICAL

Shingrix

a suspension for injection supplied as a single-dose vial of 50 mcg varicella zoster virus (VZV) glycoprotein E (gE) antigen and AS01B adjuvant

Trial Locations (4)

2100

Northern Beaches Clinical Research, Brookvale

2148

Paratus Clinical Research Western Sydney, Blacktown

2259

Paratus Clinical Research Central Coast, Kanwal

3124

Emeritus Research Melbourne, Camberwell

All Listed Sponsors
lead

Dynavax Technologies Corporation

INDUSTRY