- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07793227
Phase Ⅲ Clinical Trial of an Inactivated Hepatitis A Vaccine
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
Status
Forhold
Studietype
Registrering (Antatt)
Fase
- Fase 3
Kontakter og plasseringer
Studiekontakt
- Navn: Van Anh Thi Pham
- Telefonnummer: 84 915595690
- E-post: phamthivananh.hmu@gmail.com
Studiesteder
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-
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Hanoi, Vietnam
- Rekruttering
- Hanoi Medical University
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Ta kontakt med:
- Van Anh Thi Pham
- Telefonnummer: 84 915595690
- E-post: phamthivananh.hmu@gmail.com
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Barn
- Voksen
- Eldre voksen
Tar imot friske frivillige
Beskrivelse
Inclusion Criteria:
- Healthy participants aged 1 year and older;
- Participants (and/or their legal guardians) are able to understand and sign the informed consent voluntarily;
- 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.
- Participants should provide verifiable identification, to be contacted, and to contact the investigator during the study period.
- Participants should agree to comply with the lifestyle precautions outlined in the protocol.
Exclusion Criteria:
- Prior vaccination with any hepatitis A vaccine or combined vaccines containing HAV components;
- Prior history of HAV infection;
- 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;
- Known allergy to vaccines or vaccines ingredients;
- Autoimmune diseases, immunodeficiency diseases (including but not limited to systemic lupus erythematosus, ankylosing spondylitis, autoimmune thyroid diseases, asplenia, functional asplenia, and HIV infection);
- Coagulation disorders (e.g. factor deficiency, platelet disorders), or history of bleeding, hematoma, or bruising following intramuscular injections or venipuncture;
- 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;
- 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;
- 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;
- Receipt of blood products or immunoglobulins within 180 days prior to screening, or plans to receive these treatments in the trial;
- Receipt of other investigational drugs/vaccines within 30 days prior to screening, or plans to receive such drugs or vaccines during the study period;
- 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;
- Fever on vaccination day, with axillary temperature >37.2°C pre-vaccination, or vital signs outside normal range, or failure to pass physical examination;
- 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;
- Acute onset of various acute diseases or chronic diseases within the past 7 days, or known or suspected active infections;
- Any other factors considered by the investigator to make the participant unsuitable for participation in the trial.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Forebygging
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Firemannsrom
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
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Eksperimentell: Adult dose, treatment group (≥16 years)
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Inactivated Hepatitis A Vaccine (Human Diploid Cell) manufactured by Sinovac, adult dose (≥ 16 years)
Andre navn:
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Eksperimentell: Pediatric dose, treatment group (6~ <16 years)
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Inactivated Hepatitis A Vaccine (Human Diploid Cell) manufactured by Sinovac, pediatric dose (1~<16 years)
Andre navn:
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Aktiv komparator: Pediatric dose, control group (6~ <16 years)
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Hepatitis A vaccine (inactivated, adsorbed) manufactured by Sanofi
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Eksperimentell: Pediatric dose, treatment group (1~ <6 years)
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Inactivated Hepatitis A Vaccine (Human Diploid Cell) manufactured by Sinovac, pediatric dose (1~<16 years)
Andre navn:
|
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Aktiv komparator: Pediatric dose, conrol group (1~ <6 years)
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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
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Incidence of adverse events (AE)/adverse reactions (AR) within 30 days after each vaccination
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30 days after each vaccination
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Incidence of adverse events (AE)/adverse reactions (AR)
Tidsramme: 7 days after each vaccination
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Incidence of AE/AR within 7 days after each vaccination
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7 days after each vaccination
|
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Incidence of serious adverse events (SAE)
Tidsramme: From first vaccination to 30 days after second vaccination
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Incidence of serious adverse events (SAE) from first vaccination to 30 days after second vaccination
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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
Sponsor
Samarbeidspartnere
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- PRO-HAV-4018
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
Legemiddel- og utstyrsinformasjon, studiedokumenter
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