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Clinical Trial Summary

The objective of this study is to evaluate the safety and immunogenicity after one primary dose and one additional dose (administered twice at an interval of 6 months) of inactivated hepatitis A vaccine are administered in adolescents (16 years of age or older) or adults.


Clinical Trial Description

For this, a two-group comparison study will be conducted using a previously approved inactivated hepatitis A vaccine (Havrix Inj., manufactured by GSK) as the control vaccine to prove that the immunogenicity of the test vaccine treatment group is not inferior to the control vaccine treatment group and to statistically confirm that there is no difference in safety. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03654677
Study type Interventional
Source Boryung Pharmaceutical Co., Ltd
Contact
Status Completed
Phase Phase 3
Start date September 19, 2017
Completion date January 31, 2019

See also
  Status Clinical Trial Phase
Completed NCT03654664 - To Evaluate the Immunogenicity and Safety of Inactivated Hepatitis A Vaccine Phase 3
Completed NCT02712359 - This Study Will Evaluate the Persistence of Hepatitis A Antibodies, 8 Years and 10 Years Later, in Children Who Had Received Havrix at Selected Health Centres of Panama N/A