drugset / Trial / NCT03680417

Reactogenicity and Protectivity Following Measles- Rubella (MR) Routine Immunization in Indonesian Infants and Children

NCT03680417 ↗

Phase 4 Completed 590 enrolled PT Bio Farma
RandomizedParallel-groupSingle-blindPrevention

Summary

to assess safety and immunogenicity of measles-rubella (MR) routine immunization in Indonesian Children and Infants

Timeline

Start
2017-11-16
Primary completion
2018-02-26
Completion
2018-08-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator Measles-Rubella (MR) Vaccine Vaccine 0.5 ml —

Indications

No indication recorded.