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
| Type | Name | Description |
|---|---|---|
| BIOLOGICAL | MeMuRu-OKA (study vac) | |
| BIOLOGICAL | MMR, 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.