To evaluate the safety, immune-response and efficacy of GSK Biologicals' EBV vaccine in a population at risk of developing infectious mononucleosis. Each subject will receive three doses of vaccine or placebo during the study period.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Enrollment
200
GSK Clinical Trials Call Center
Brussels, Belgium
Attack rates of infectious mononucleosis over 18 months after Dose 2
Solicited symptoms (Day 0-7); unsolicited AEs (Day 0-29 ); SAEs (full study)
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