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HPAIV_H5N8

An open-label Phase II study to evaluate the immunogenicity and safety of CH5-AS - HPAIV_H5N8

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2031240648
Enrollment
70
Registered
2025-01-30
Start date
2025-01-30
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy adults

Interventions

Sponsors

Ohmagari Norio
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Healthy adults aged 18 years or older who have not yet been vaccinated against the H5 subtype

Exclusion criteria

Exclusion criteria: 1) Individuals who have a clear history of H5 subtype influenza (as reported by the subject) 2) Individuals who have previously experienced anaphylaxis due to food, medication or other substances 3) Individuals who have a current history of serious diseases affecting the cardiovascular, hematological, respiratory, hepatic, renal, gastrointestinal, or neuropsychiatric systems. 4) Individuals with a history of Guillain-Barre syndrome or acute disseminated encephalomyelitis 5) Individuals with confirmed influenza infection during the current season (2024/2025) (up to the first vaccination)

Design outcomes

Primary

MeasureTime frame
Immunogenicity against A/H5 subtype avian influenza virus (HI antibody titer, etc.)

Secondary

MeasureTime frame
Side reactions and adverse events. In the event that the HPAIV H5 subtype belonging to Clade 2.3.4.4b becomes a pandemic influenza in the future, serum samples will be stored at the National Institute of Infectious Diseases to estimate the effectiveness of this stockpile vaccine.

Contacts

Public ContactNorio Ohmagari

Center Hospital of the National Center for Global Health and Medicine

H5N8@hosp.ncgm.go.jp+81-3-5273-5419

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026