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Clinical Trial Summary

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


Clinical Trial Description

- to asses serious immediate systemic events,

- to assess local and systemic reaction after Measles-Rubella (MR) vaccine in infants and children,

- to evaluate protectivity and antibody response to measles and rubella after 1 dose of MR vaccine ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03680417
Study type Interventional
Source PT Bio Farma
Contact
Status Completed
Phase Phase 4
Start date November 16, 2017
Completion date August 1, 2018

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