The purpose of this study is to determine the safety and immunogenicity of the recombinant hepatitis E vaccine in people older than 65 years, and evaluate the efficacy of hepatitis E vaccine in this population.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
601
Center for disease control and prevention in Xiamen haicang district
Xiamen, Fujian, China
Number of Participants with Serious and Non-Serious Adverse Events
Any adverse events reported within one month post each vaccination would be recorded, any serious adverse events reported throughout the study would be recorded.
Time frame: From month 0-7
anti-HEV IgG seropositive rate
Time frame: at month 7
GMT of anti-HEV IgG
Serum sample would be collected at month 7, and geometric mean titer of anti-HEV IgG would be tested
Time frame: 7 month after first vaccination
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