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Phase Ⅲ Clinical Trial of an Inactivated Hepatitis A Vaccine

25. august 2026 oppdatert av: Sinovac Biotech Co., Ltd

A Phase Ⅲ Clinical Trial to Evaluate the Immunogenicity and Safety of an Inactivated Hepatitis A Vaccine (Human Diploid Cell) in Healthy Adults and Children Aged ≥1 Year

This is a Phase Ⅲ, open-label, single arm design combined with randomized, double-blind, active-controlled design trial to assess the immunogenicity and safety of different specifications of Healive® (the 0.5 mL pediatric dosage and the 1 mL adult dosage).

A total of 680 healthy participants aged 1 year and above will be enrolled, including 200 participants aged 16 years and older (adult dose group), and 480 participants aged 1 to less than 16 years (pediatric dose group).

For the adult dose group: open-label, single-arm design, 200 participants aged 16 years and above will be enrolled to receive Healive® (1.0 mL).

For the pediatric dose group: double-blinded, randomized, positive-controlled design, 480 participants aged 1 to less than 16 years will be enrolled, and randomized in a 2:1 ratio to receive either Healive® (0.5 mL) or Avaxim® (0.5 mL). All participants will receive two doses of either Healive® or Avaxim® at 0 and 6 months.

Studieoversikt

Studietype

Intervensjonell

Registrering (Antatt)

680

Fase

  • Fase 3

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Barn
  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Ja

Beskrivelse

Inclusion Criteria:

  1. Healthy participants aged 1 year and older;
  2. Participants (and/or their legal guardians) are able to understand and sign the informed consent voluntarily;
  3. Participants of reproductive potential and their sexual partners should voluntarily use effective contraception from signing the ICF to 30 days after the second vaccination and avoid donating sperm or eggs.
  4. Participants should provide verifiable identification, to be contacted, and to contact the investigator during the study period.
  5. Participants should agree to comply with the lifestyle precautions outlined in the protocol.

Exclusion Criteria:

  1. Prior vaccination with any hepatitis A vaccine or combined vaccines containing HAV components;
  2. Prior history of HAV infection;
  3. Female participants of reproductive potential who are pregnant (including a positive urine pregnancy test) or have a pregnancy plan within 30 days after the second vaccination, or who are currently lactating;
  4. Known allergy to vaccines or vaccines ingredients;
  5. Autoimmune diseases, immunodeficiency diseases (including but not limited to systemic lupus erythematosus, ankylosing spondylitis, autoimmune thyroid diseases, asplenia, functional asplenia, and HIV infection);
  6. Coagulation disorders (e.g. factor deficiency, platelet disorders), or history of bleeding, hematoma, or bruising following intramuscular injections or venipuncture;
  7. Poorly controlled chronic illnesses or history of severe diseases that, including but not limited to cardiovascular diseases, hematological disorders, liver and kidney diseases, digestive system disorders, respiratory diseases, malignancies, and a history of major organ transplantation;
  8. Current or history of severe neurological diseases [epilepsy, convulsions or seizures (excluding history of febrile seizures)] or psychiatric disorders, or presence of a family history of psychiatric disorders;
  9. Receipt of ≥14 days of immunosuppressive or other immunomodulatory therapy (prednisone ≥20mg/day, or prednisone ≥2mg/kg/day, or its equivalent), cytotoxic therapy within 180 days prior to screening, or plans for such treatment during the trial;
  10. Receipt of blood products or immunoglobulins within 180 days prior to screening, or plans to receive these treatments in the trial;
  11. Receipt of other investigational drugs/vaccines within 30 days prior to screening, or plans to receive such drugs or vaccines during the study period;
  12. Receipt of attenuated live vaccines or nucleic acid vaccines within 14 days prior to screening, or subunit or inactivated vaccines within 7 days prior to screening;
  13. Fever on vaccination day, with axillary temperature >37.2°C pre-vaccination, or vital signs outside normal range, or failure to pass physical examination;
  14. Presence of skin injuries, inflammation, ulcers, rashes, scars, or other conditions at the intended injection site that may interfere with drug administration or observation of local reactions;
  15. Acute onset of various acute diseases or chronic diseases within the past 7 days, or known or suspected active infections;
  16. Any other factors considered by the investigator to make the participant unsuitable for participation in the trial.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Forebygging
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Firemannsrom

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Adult dose, treatment group (≥16 years)
Inactivated Hepatitis A Vaccine (Human Diploid Cell) manufactured by Sinovac, adult dose (≥ 16 years)
Andre navn:
  • Healive® (1 mL)
Eksperimentell: Pediatric dose, treatment group (6~ <16 years)
Inactivated Hepatitis A Vaccine (Human Diploid Cell) manufactured by Sinovac, pediatric dose (1~<16 years)
Andre navn:
  • Healive® (0.5 mL)
Aktiv komparator: Pediatric dose, control group (6~ <16 years)
Hepatitis A vaccine (inactivated, adsorbed) manufactured by Sanofi
Eksperimentell: Pediatric dose, treatment group (1~ <6 years)
Inactivated Hepatitis A Vaccine (Human Diploid Cell) manufactured by Sinovac, pediatric dose (1~<16 years)
Andre navn:
  • Healive® (0.5 mL)
Aktiv komparator: Pediatric dose, conrol group (1~ <6 years)
Hepatitis A vaccine (inactivated, adsorbed) manufactured by Sanofi

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Seroconversion rate of anti-HAV antibodies
Tidsramme: 30 days after the second vaccination
The seroconversion rate of anti-hepatitis A virus (HAV) antibodies 30 days after the second vaccination
30 days after the second vaccination

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Seropositive rate of anti-HAV antibodies
Tidsramme: 30 days after the second vaccination
The seropositive rate of anti-HAV antibodies 30 days after the second vaccination
30 days after the second vaccination
Geometric mean concentration (GMC) of anti-HAV antibodies
Tidsramme: 30 days after the second vaccination
The geometric mean concentration (GMC) of anti-HAV antibodies 30 days after the second vaccination
30 days after the second vaccination
Geometric mean fold rise (GMFR) of anti-HAV antibodies
Tidsramme: 30 days after the second vaccination
The geometric mean fold rise (GMFR) of anti-HAV antibodies 30 days after the second vaccination
30 days after the second vaccination
Incidence of adverse events (AE)/adverse reactions (AR)
Tidsramme: 30 days after each vaccination
Incidence of adverse events (AE)/adverse reactions (AR) within 30 days after each vaccination
30 days after each vaccination
Incidence of adverse events (AE)/adverse reactions (AR)
Tidsramme: 7 days after each vaccination
Incidence of AE/AR within 7 days after each vaccination
7 days after each vaccination
Incidence of serious adverse events (SAE)
Tidsramme: From first vaccination to 30 days after second vaccination
Incidence of serious adverse events (SAE) from first vaccination to 30 days after second vaccination
From first vaccination to 30 days after second vaccination

Andre resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
The seroconversion rate of HAV antibodies
Tidsramme: 30 days after the second vaccination
The seroconversion rate of HAV antibodies 30 days after the second vaccination in susceptible population
30 days after the second vaccination
The seropositive rate of anti-HAV antibodies
Tidsramme: 30 days after the first vaccination
The seropositive rate of anti-HAV antibodies 30 days after the first vaccination
30 days after the first vaccination
The seroconversion rate of anti-HAV antibodies
Tidsramme: 30 days after the first vaccination
The seroconversion rate of anti-HAV antibodies 30 days after the first vaccination
30 days after the first vaccination
The GMC of anti-HAV antibodies
Tidsramme: 30 days after the first vaccination
The GMC of anti-HAV antibodies 30 days after the first vaccination
30 days after the first vaccination
The GMFR of anti-HAV antibodies
Tidsramme: 30 days after the first vaccination
The GMFR of anti-HAV antibodies 30 days after the first vaccination
30 days after the first vaccination

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Samarbeidspartnere

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

20. august 2026

Primær fullføring (Antatt)

15. september 2027

Studiet fullført (Antatt)

15. september 2027

Datoer for studieregistrering

Først innsendt

25. august 2026

Først innsendt som oppfylte QC-kriteriene

25. august 2026

Først lagt ut (Faktiske)

28. august 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

28. august 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

25. august 2026

Sist bekreftet

1. august 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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