Investigational Procedure: It consists of prospective blood and saliva collections. Study without any IMP administration.
Study summary
This multi-center, prospective, longitudinal cohort study is designed to gather immunological and clinical data on EBV reactivation in EBV seropositive adults aged 18 to 29 years.
This study will follow a cohort of approximately 100 EBV seropositive adults 18 to 29 years of age in Australia over a 6 or 12-month period.
Participants will not receive any study intervention (eg, study treatments, vaccines).
Eligibility
Sex
ALL
Min age
18 Years
Max age
29 Years
Healthy volunteers
Accepted
Inclusion Criteria:
* Aged 18 to 29 years on the day of inclusion
* Participants who are healthy as determined by medical evaluation including medical history and physical examination
* Participants who are EBV seropositive based on serology testing
Exclusion Criteria:
Any condition which in the opinion of the investigator might interfere with the evaluation of the study objectives, including planning to leave the area of the study before the end of study period
The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
Primary outcome measure(s)
Number of participants with EBV DNA in blood and saliva at each study visit — 6 or 12 months
Serology testing indicative of EBV reactivation, measured by anti-VCA IgG/IgM, anti-EBNA-1 IgG and anti-EA IgG at each study visit — 6 or 12 months
Trial sites (2)
Facility
City
Region
Status
Griffith - University Clinical Trial Unit - Site Number : 0360001
Gold Coast
Australia
University of Sunshine Coast - Site Number : 0360002
South Brisbane
Australia
More Sanofi Pasteur, a Sanofi Company trials in Australia
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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