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Clinical Trial Summary

The purpose of this study is to evaluate the persistence of hepatitis A antibodies, approximately 8 years and 10 years post vaccination with the complete series of Havrix (2 doses) and the partial series completion (1 dose).


Clinical Trial Description

The study comprises of two independent cross-sectional surveys (Year 8 and Year 10). The first cross-sectional serosurvey will evaluate the long term persistence of immunity approximately 8 years post vaccine administration and the second cross-sectional study will evaluate long term persistence, approximately 10 years post vaccine administration. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02712359
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase N/A
Start date June 1, 2016
Completion date August 22, 2018

See also
  Status Clinical Trial Phase
Completed NCT03654677 - To Evaluate the Immunogenicity and Safety of Inactivated Hepatitis A Vaccine (VITHA-A) Phase 3
Completed NCT03654664 - To Evaluate the Immunogenicity and Safety of Inactivated Hepatitis A Vaccine Phase 3