drugset / Trial / NCT01014845

Summary

The primary purpose of this study is to determine whether the preventive hepatitis E are effective in the prevention of hepatitis E occurring at least 30 days after the administration of the third dose of vaccine. The secondary purpose of this study is to to evaluate the safety and immunogenicity and immunopersistence of the study vaccine. The initial study is planed to be ended on month 19 and the results were analysed and used for registration purpose. The extended study will be continued to assess the long-term efficacy, immunogenicity and safety.

Timeline

Start
2007-08
Primary completion
2017-10
Completion
2017-10

Outcome

Met primary endpoint

paper 15 per-protocol participants in the placebo group developed hepatitis E compared with none in the vaccine group. PMID 20728932 ↗

paper Vaccine efficacy after three doses was 100.0% (95% CI 72.1-100.0). PMID 20728932 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject HEV239 Vaccine 30 ug Intramuscular