drugset / Trial / NCT00891007

Study to Evaluate Safety, Dose Response and Immunogenicity of the Measles Vaccine MVA mBN85B in Healthy Children Aged 6 Months to 6 Years

NCT00891007

Phase 2 Completed 90 enrolled Bavarian Nordic
RandomizedParallel-groupOpen-labelPrevention

Summary

Partially randomized, controlled Phase II study to evaluate safety, immunogenicity and dose response of the measles vaccine MVA mBN85B in healthy children aged 6 months to 6 years.

Timeline

Start
2009-06
Primary completion
2010-07
Completion
2010-08

Drugs

EvaluationDrugModalityDoseRoute
Subject MVA mBN85B Vaccine 1e+07 unknown Subcutaneous
Subject MVA mBN85B Vaccine 1e+08 unknown Subcutaneous
Comparator Rouvax Vaccine 0.5 ml Subcutaneous
Comparator Rouvax Vaccine 1000 unknown Subcutaneous

Indications