Immunogenicity and Safety of a Combined Vaccine to Prevent Measles, Mumps, Rubella and Chickenpox Diseases
Phase 3
Completed
- Conditions
- MeaslesMumpsRubellaVaricella
- Registration Number
- NCT00127010
- Lead Sponsor
- GlaxoSmithKline
- Brief Summary
This is a study to evaluate the immunogenicity and safety of GlaxoSmithKline (GSK) Biologicals combined measles-mumps-rubella varicella candidate vaccine given to healthy children in their second year of life.
- Detailed Description
This study included an active control group who received the licensed Priorix (measles, mumps, rubella \[MMR\] vaccine).
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria
- A male or female subject between 11-13 months of age (i.e. from 11 month birthday until the day before the 14 month birthday) at the time of the first vaccination.
Exclusion Criteria
- History of previous measles, mumps, rubella and/or varicella vaccination or disease, or known exposure to any of these diseases within 30 days prior to the start of the trial
- Planned administration of a vaccine not foreseen by the study protocol from 30 days prior to each vaccination until 42-56 days after each vaccination
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Antibody levels after vaccination
- Secondary Outcome Measures
Name Time Method Safety of the study vaccines
Trial Locations
- Locations (1)
GSK Investigational Site
🇳🇱Rotterdam, Netherlands