Clinical Trials Directory

Trials / Completed

CompletedNCT00352898

Immunogenicity, Safety of Measles-mumps-rubella-varicella Vaccine (MeMuRu-OKA) Compared to Priorix™ Given With Varilrix™

Comparative Study Evaluating the Immunogenicity & Safety of MeMuRu-OKA Vaccine & Measles-mumps-rubella Vaccine (Priorix™) Co-administered With Varicella Vaccine (Varilrix™) in Children Primed With Both Measles-mumps-rubella & Varicella Vaccines

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
400 (actual)
Sponsor
GlaxoSmithKline · Industry
Sex
All
Age
15 Months – 6 Years
Healthy volunteers
Accepted

Summary

Since measles-mumps-rubella (MMR) and varicella vaccinations are established as routine childhood practice and often co-administered during the second year of life, a combined measles-mumps-rubella-varicella (MeMuRu-OKA) vaccine is fully justified. Such a combined vaccine was developed and extensively studied in susceptible children. In countries where varicella mass-vaccination is already implemented, a transition period is necessary as children who started with separate first-dose vaccinations of MMR and varicella will receive a single shot of the combined vaccine as the second dose. To account for those situations, this study will evaluate the effect of the combined measles-mumps-rubella-varicella vaccine given in place of separate MMR and varicella vaccines as a second dose.

Conditions

Interventions

TypeNameDescription
BIOLOGICALMeMuRu-OKA (study vac)
BIOLOGICALMMR, Varicella vacc (control)

Timeline

Start date
2006-04-01
Completion
2006-11-01
First posted
2006-07-17
Last updated
2016-10-07

Locations

6 sites across 2 countries: Canada, Italy

Source: ClinicalTrials.gov record NCT00352898. Inclusion in this directory is not an endorsement.