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Immunogenicity and Safety of I-HAV in Healthy Thai Children and Adolescents Lacking Protective Antibody After L-HAV

Immunogenicity and Safety of I-HAV in Healthy Thai Children and Adolescents Lacking Protective Antibody After L-HAV

Recruiting
18-20 years
All
Phase 3

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Overview

Hepatitis A virus (HAV) remains a common infection in Thai children. Two HAV vaccines are available: inactivated vaccine (I-HAV, 2 doses) and live-attenuated vaccine (L-HAV, single dose), but neither is included in Thailand's national immunization program. Our previous randomized, active-controlled, open-label, non-inferiority trial trial found that some participants remained seronegative after one L-HAV dose (anti-HAV IgG <1 S/CO) (preliminary data). This study aims to evaluate the immunogenicity and safety of an additional dose of I-HAV in healthy Thai children and adolescents who did not develop protective antibody levels after a single dose of L-HAV.

Description

Hepatitis A virus (HAV) infection remains a common cause of viral hepatitis among children and adolescents in developing countries, including Thailand. Currently, two types of HAV vaccines are available in Thailand; (1) inactivated HAV vaccine (I-HAV) which is recommended as a 2-dose series administered 6 months apart, approved for use in children aged 1 year and older, and (2) live-attenuated HAV vaccine (L-HAV) which is recommended as a single dose, approved for children aged 18 months and older. However, as neither vaccine is included in Thailand's Expanded Programme on Immunization (EPI), the national vaccination coverage remains suboptimal.

In 2024, the investigators conducted a randomized, active-controlled, open-label, non-inferiority trial to compare the immunogenicity and safety of the currently marketed I-HAV and L-HAV in healthy Thai children and adolescents aged 18 months to 18 years. Preliminary results showed that a proportion of participants remained seronegative following a single dose of L-HAV (anti-HAV IgG <1 S/CO). Based on these findings, the investigators hypothesize that an additional dose of I-HAV may be necessary to achieve adequate seroprotection in this population. Therefore, the aim of this study is to evaluate the immunogenicity and safety of an additional dose of I-HAV in healthy Thai children and adolescents who did not develop protective antibody levels after a single dose of L-HAV.

Eligibility

Inclusion Criteria:

  • Thai children and adolescents who previously participated in the previous RCT study
  • Previously randomized to receive one dose of L-HAV vaccine within the past 1 year (+/- 2 months)
  • Have not demonstrate a seropositivity against HAV (anti-HAV IgG <1 S/CO) at 1 month after L-HAV vaccination
  • Participants and/or caregivers gives written inform consent/assent form

Exclusion Criteria:

  • History of acute illness within 4 weeks prior to study enrollment
  • Has a history of illness or a diagnosis consistent with hepatitis A after receiving the live attenuated hepatitis A vaccine as part of participation in a previous research study
  • Has a history of receiving any additional hepatitis A vaccine after participating in the previous research study
  • Presence of fever (body temperature ≥38.0°C), jaundice, or yellowing of the eyes within 4 weeks prior to study enrollment
  • Has underlying conditions including thrombocytopenia, coagulopathy, hemophilia A or B, neurological disorders, immunodeficiency disorders, chronic liver disease, or chronic hepatitis B or C infection
  • Has received immunosuppressive agents, immunomodulatory agents, or high-dose corticosteroids (greater than 2 mg/kg/day or more than 20 mg/day) for more than 14 consecutive days within 6 months prior to study enrollment
  • Has received blood products or blood components, including immunoglobulins, within 6 months prior to study enrollment
  • Has received other live vaccines within 30 days prior to study enrollment
  • Has history of allergy to vaccines or any vaccine components, such as aluminum hydroxide, 2-phenoxyethanol, neomycin, formaldehyde, or gentamicin sulfate, or has history of severe allergic reactions (e.g., anaphylaxis) to any vaccines
  • Women planning for pregnancy, pregnant women or lactating women
  • Women in childbearing age who cannot use contraceptive methods during study participation
  • Is concurrently involved in other clinical trials in which receiving an investigational vaccine or study drug as part of study participation
  • Have any condition that, in the opinion of the site investigator, would compromise the subject's ability to participate in the study

Study details
    Hepatitis A
    Hepatitis A Virus
    Vaccine-Preventable Diseases

NCT06978621

Chiang Mai University

21 October 2025

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