drugset / Trial / NCT06667206

Earlier Prime-BOOST Schedule to Improve MEasles Protection in High Burden Settings

NCT06667206 ↗

RandomizedParallel-groupOpen-labelPrevention

Summary

This is a phase IIb clinical trial investigating the non-inferiority of immune responses in children given two doses of measles vaccine at different timepoints. The study will randomise 450 children to 3 groups: group A will receive measles containing vaccine (MCV) at 6 and 12 months ; group B at 9 and 18 months; Group C at 6 and 18 months.

Timeline

Start
2023-11-15
Primary completion
2026-05-10
Completion
2026-05-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Licenced Measles-Rubella vaccine Vaccine — —

Indications