Viewing Study NCT00353288



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Study NCT ID: NCT00353288
Status: COMPLETED
Last Update Posted: 2016-10-07
First Post: 2006-07-17

Brief Title: Immunogenicity Safety of Measles-mumps-rubella-varicella Vaccine MeMuRu-OKA Compared to Priorix Given With Varilrix
Sponsor: GlaxoSmithKline
Organization: GlaxoSmithKline

Study Overview

Official Title: Comparative Study Evaluating the Immunogenicity and Safety of MeMuRu-OKA Vaccine and Measles-mumps-rubella Vaccine Priorix Co-administered With Varicella Vaccine Varilrix in Children Primed With Measles-mumps-rubella Vaccine
Status: COMPLETED
Status Verified Date: 2016-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: As measles-mumps-rubella MMR vaccination is established as routine childhood practice in most industrialised countries and varicella vaccination is now being introduced in many countries during the second year of life a combined measles-mumps-rubella-varicella vaccine was developed for administration convenience and improved compliance to vaccination To account for situations where children have received a first dose of MMR vaccine without varicella this study will evaluate the effect of the combined measles-mumps-rubella-varicella vaccine given in place of the second dose of MMR vaccine A second dose of the monovalent varicella vaccine will be given to all children participating to this trial since there is a current debate on the need of a second dose to induce a full protection against varicella
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None