drugset / Trial / NCT01702428

Consistency Study of GlaxoSmithKline (GSK) Biologicals' MMR Vaccine (209762) (Priorix) Comparing Immunogenicity and Safety to Merck & Co., Inc.'s MMR Vaccine (M-M-R II), in Children 12 to 15 Months of Age

NCT01702428

Phase 3 Completed 5016 enrolled GlaxoSmithKline
RandomizedParallel-groupTriple-blindPrevention

Summary

The purpose of this study is to evaluate consistency in terms of the immune response to three different lots of GSK Biologicals' trivalent MMR vaccine manufactured to target potencies, and compare its immunogenicity to Merck \& Co., Inc.'s MMR vaccine, which is approved for use in the United States (US).

Timeline

Start
2012-11-09
Primary completion
2014-11-25
Completion
2015-04-16

Drugs

EvaluationDrugModalityDoseRoute
Comparator M-M-R II Vaccine 1 unknown Subcutaneous
Subject Priorix Vaccine 1 unknown Subcutaneous
Background Havrix Vaccine 1 unknown Intramuscular
Background Prevnar 13 Vaccine 1 unknown Intramuscular
Background Varivax Vaccine 1 unknown Subcutaneous