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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06058416
Study type Interventional
Source Sinovac Biotech Co., Ltd
Contact
Status Active, not recruiting
Phase Phase 4
Start date October 24, 2023
Completion date December 31, 2029

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