Japanese Encephalitis Clinical Trial
Official title:
Ability of the New Vero-cell-derived Inactivated Japanese Encephalitis Vaccine (IXIARO) to Elicit a Booster Response in Travellers Previously Vaccinated With Traditional Mouse-brain Derived Vaccine (JE-MB)
Verified date | October 2011 |
Source | Helsinki University Central Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | Finland: Finnish Medicines Agency |
Study type | Interventional |
The old mouse brain derived Japanese encephalitis vaccines (MBJEV) have been reported to
cause serious adverse effects and are therefore replaced with the novel Ixiaro vaccine. The
present study investigates whether vaccinees primed with MBJEV can be boosted with Ixiaro.
Travellers receiving Japanese encephalitis vaccines are enrolled for a follow-up of immune
responses in four groups: A) primary immunization with BMJEV, B) primary and secondary
immunizations with MBJEV, C) primary immunizations with Ixiaro and S) Primary immunization
with MBJEV and secondary immunization with Ixiaro. Immune responses are followed with help
of serum samples collected before and after vaccination.
Status | Completed |
Enrollment | 120 |
Est. completion date | April 2011 |
Est. primary completion date | April 2011 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Male and female travellers = 18 years of age. - General good health. - Written informed consent. - Ability to attend all visits scheduled in this study. - Travellers who have previously got a primary vaccination series of 2 or 3 doses of JE-MB and now receive a booster vaccination , either MB-JEV or IXIARO, at the travel clinic for their journey to Asia, OR - Travellers with no previous vaccination against JE who are given the primary vaccination series with IXIARO at a travel clinic prior to their journey to Asia. Exclusion Criteria: - - < 18 years of age. - Acute disease at the time of enrollment. - Pregnancy or lactation. - Known immunodeficiency or immune suppressive treatment. - Any chronic illness that might interfere with the immune response; history of JE. - Alcohol or drug abuse. - Any clinically significant history of known or suspected anaphylaxis or hypersensitivity (based on the investigator's judgement). |
Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Helsinki University Central Hospital | Karolinska Institutet |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Antibody titers 1 month after last vaccine dose | Determination of antibody titers 1 month after last vaccine dose | 1 month | No |
Secondary | Antibody titers two years after vaccination | Measurement of antibody titers two years after vaccination | 2 years | No |
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