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Active, not recruiting Phase 1/2

Safety and Immunogenicity of an Investigational Herpes Zoster Vaccine (Z-1018) Compared to Shingrix® in Healthy Adults 50 Years of Age and Over

NCT06569823 · tracked via the Priya Life Science Australia tracker
Sponsor
Dynavax Technologies Corporation
Phase
Phase 1/2
Started
2024-06-17
Last updated
2026-05-29

Condition(s) studied

ShinglesHerpes ZosterVaccine-Preventable Diseases

Investigational drug(s) / intervention(s)

Z-1018Shingrix →

Z-1018: Formulation for injection

Shingrix: Formulation for injection

Study summary

This is a randomized, active-controlled, observer-blinded, dose-escalation multi-center trial of 2 doses of an investigational HZ vaccine (Z-1018) in approximately 764 healthy adults.

Eligibility

Sex
ALL
Min age
50 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: 1. Willing to participate; informed consent provided for the study 2. Male or female ≥ 50 years of age (Part 1: 50 through 69 years of age, inclusive; Part 2: ≥ 70 years of age 3. In good health in the opinion of the investigator, based upon medical history, physical examination, and laboratory evaluation 4. Able to comprehend and follow all required trial procedures and be available for all visits scheduled in the trial 5. Seronegative for human immunodeficiency virus (HIV), hepatitis B virus (HBV), and hepatitis C virus (HCV) as assessed during Screening 6. If female of child-bearing potential and heterosexually active, has practiced adequate contraception for at least 28 days prior to vaccination, has negative pregnancy tests just prior to vaccination, and has agreed to continue adequate contraception through 3 months following the final study injection. Exclusion Criteria: 1. History of HZ 2. Previous vaccination against varicella (chicken pox) or HZ 3. Febrile illness within 7 days of the first trial injection (defined as at least 1 measured body temperature of ≥ 38°C, regardless of route of measurement) 4. Confirmed SARS-CoV-2/COVID-19 infection as assessed during Screening within 7 days of first trial injection. 5. If female of childbearing potential, is pregnant (known before or established at the time of screening), breastfeeding, or planning a pregnancy or to breastfeed 6. Known or suspected immunodeficiency (including but not limited to HIV/AIDS), or immunocompromised state, as assessed by medical history, past or current laboratory studies, and/or physical examination 7. History of sensitivity to any component of the trial vaccines 8. Has received the following prior to Day 1 trial injection: a) ≤ 14 days: i) Any licensed or authorized inactivated vaccines (including vaccines containing mRNA or CpG) b) ≤ 28 days: i) Any live vaccine ii) Systemic corticosteroids (≥ 20 mg/ day of prednisone or equivalent for more than 14 consecutive days) or other immunomodulators or immune suppressive medication, with the exception of inhaled steroids iii) Any investigational medicinal agent c) ≤ 90 days: i) Granulocyte or granulocyte-macrophage colony-stimulating factor ii) Immunoglobulins or any blood products (receipt of certain monoclonal antibodies may on a case-by-case basis be non-exclusionary if approved via consultation with Sponsor Medical Monitor) iii) Antisense oligonucleotides iv) Drugs/investigational agents with very long half-lives (defined as ≥ 60 days) (eg, radioactive iodine-125, amiodarone, nirsevimab, and evinacumab) v) Infusion of blood products d) ≤ 6 months before Day 1 (or likely to require during the trial period): i) chronic administration of immunosuppressants or other immune-modifying drugs e) At any time: DNA plasmids or other genetic therapy intended to integrate permanently into host cells 9. Is undergoing chemotherapy or expected to receive chemotherapy during the trial period; and/or has a diagnosis of cancer within the last 5 years other than squamous cell or basal cell carcinoma of the skin 10. History or current evidence of any condition, therapy, laboratory abnormality, or other finding that might confound the results of the trial, interfere with the participant's participation for the full duration of the trial, or is not in the best interest of the participant to participate, in the opinion of the treating investigator 11. Underlying chronic medical condition requiring ongoing follow-up and monitoring by a healthcare provider that might affect the immune response to vaccine (eg, diabetes mellitus, chronic kidney disease) 12. Known psychiatric or substance abuse disorder that would interfere with cooperation with the requirements of the trial 13. Current or historical autoimmune disease 14. Any skin condition and/or tattoo on both arms that may interfere with the evaluation of safety at the injection site, in the opinion of the treating investigator 15. Any other finding that the Investigator considers will make the participant unsuitable for the trial or unable to comply with the trial requirements

Primary outcome measure(s)

  • Part 1 and Part 2: Percentage of participants with solicited local and systemic post-injection reactions (PIRs) — Up to 7 days following each dose
    Solicited local and systemic post-injection reactions (PIRs)
  • Part 1 and Part 2: Percentage of participants with Adverse events (AEs) — 28 days following each dose
    Adverse events (AEs)
  • Part 1 and Part 2: Percentage of participants with serious adverse events (SAEs), medically-attended adverse events (MAEs), and immune-mediated adverse events of special interest (imAESIs) — Day 1 through 12 months after the last dose of study injection
    Serious adverse events (SAEs) Medically-attended adverse events (MAEs) Immune-mediated adverse events of special interest (imAESIs)
  • Part 2: Vaccine response — 4 weeks after the second study injection
    Composite vaccine response rate in glycoprotein E (gE) -specific CD4+ T cells and anti-gE IgG antibodies in the Per Protocol (PP) population
  • Part 2: Anti-gE IgG antibody concentration — 4 weeks after the second study injection
    Geometric mean concentration (GMC) and geometric mean ratio of IgG antibodies to varicella-zoster virus (VZV) antigen-gE in the Per Protocol (PP) population

Trial sites (16)

FacilityCityRegionStatus
Paratus Clinical Research Western Syndney Blacktown New South Wales
Emeritus Research Botany New South Wales
Canopy Clinical Northern Beaches Brookvale New South Wales
Paratus Clinical Research Central Coast Kanwal New South Wales
Sutherland Shire Clinical Research Miranda New South Wales
Innovate Clinical Research Waitara New South Wales
Canopy Clinical Wollongong Wollongong New South Wales
Paratus Clinical Research Brisbane Herston Queensland
Veritus Research Bayswater Victoria
Emeritus Research Camberwell Victoria
Doherty Clinical Trials Limited East Melbourne Victoria
Optimal Clinical Trials Ltd - North Auckland New Zealand
Optimal Clinical Trials Ltd - Central Auckland New Zealand
New Zealand Clinical Research Christchurch New Zealand
Momentum Wellington Wellington New Zealand
Momentum Clinical Research Kapiti Wellington New Zealand
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06569823 on ClinicalTrials.gov ↗ ← All trials in Australia