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ACTIVE NOT RECRUITING
NCT06058416
PHASE4

Immunogenicity and Safety of Hepatitis A Among People Aged 18-50 Years Old

Sponsor: Sinovac Biotech Co., Ltd

View on ClinicalTrials.gov

Summary

This study is conducted among people aged 18-50 in Dandong City, an area with a high incidence of hepatitis A in recent years. 1000 qualified pariticipants with signed informed consent will be screened for anti-HAV antibodies by collecting blood sample of 3ml. One dose of hepatitis A vaccine will be administrated to all the pariticipants. Negative anti-HAV antibodies-negative subjects will recieve the second dose of hepatitis A vaccination, and 400 of them will be randomly selected and assigned to 4 groups with different interval of vaccination(6 month, 18 months, 36 months and 60 months). Blood samples will be collected before vaccination of each dose and on 28 days after each dose of vaccination to anti-HAV antibody test. Safety data will be collected within 28 days after each vaccination with a smartphone mini-program.

Official title: The Immunogenicity and Safety of Different Vaccination Interval of Inactivated Hepatitis A Vaccine in People Aged 18-50 Years, a Phase IV Clinical Trial

Key Details

Gender

All

Age Range

18 Years - 50 Years

Study Type

INTERVENTIONAL

Enrollment

1092

Start Date

2023-10-24

Completion Date

2029-12-31

Last Updated

2024-08-21

Healthy Volunteers

Yes

Conditions

Interventions

BIOLOGICAL

Healive (hepatitis A vacine(human diploid cell), inactivated)

The hepatitis A vaccine contains 500 SU inactivated hepatitis A virus per dose in 1mL of aluminum hydroxide solution. For anti-HAV antibody-negative participants, two dose of hepatitis A vaccine will be given with vaccination interval of 6 month, 18 months, 36 months, and 60 months, respectively.

Locations (1)

Liaoning Center for Disease Control and Prevention

Shenyang, Liaoning, China