Expired Study
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Tampa, Florida


Purpose:

The study investigates long-term immunity and safety of IC51 (IXIARO®, JESPECT®) in a pediatric population vaccinated in the parent study IC51-322.


Criteria:

Inclusion Criteria: - Subjects who have received two vaccinations in study IC51 322. (2) Subjects who were enrolled as part of the immunogenicity subgroup of study IC51‐322. - Male or female healthy subjects aged ≥ 9 months to < 21 years at the time of enrolment into this study. - Written informed consent by the subject, the subject's legal representative(s), according to local requirements, and written informed assent of the subject, if applicable. Exclusion Criteria: - History of or clinical manifestation of any Flavivirus disease during study IC51‐322. - Vaccination against JE virus (JEV) (except with IC51) at any time prior or planned during this study. - Participation in another study with an investigational product during study IC51‐322 or IC51‐324. - History of or development of any immunodeficiency including post‐organtransplantation after inclusion into study IC51‐322. - History of or development of an autoimmune disease during study IC51‐322. - Administration of chronic (defined as more than 14 days) immunosuppressants or other immune‐modifying medications started during study IC51‐322 up to first visit of study IC51‐324. (For corticosteroids this means prednisone or equivalent at >= 0.05 mg/kg/day. Topical or inhaled steroids are allowed). - Known infection with human immunodeficiency virus (HIV), hepatitis B virus (HBV) or hepatitis C virus (HCV). - Illicit drug use and/or a history of drug or alcohol addiction and/or current drug or alcohol addiction. - Inability or unwillingness by the legal representative(s) and/or the subject (where applicable) to provide informed consent/assent and to abide by the requirements of the study. - Persons who are committed to an institution (by virtue of an order issued either by the judicial or the administrative authorities).


NCT ID:

NCT01246479


Primary Contact:

Study Chair
Andrea Ayad, Dr.
Valneva Austria GmbH


Backup Contact:

N/A


Location Contact:

Tampa, Florida
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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