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Clinical Trial Summary

Thus study is a clinical trial for Measles and Rubella vaccine that will be used inIndonesian National Program of Immunization. The study design will be randomized, observer blind, prospective intervention study.


Clinical Trial Description

The objectives of the study are:

- To assess the protectivity rate of Bio Farma's Measles/Rubella (MR) vaccine in infants

- To describe antibody response to Measles and Rubella after 1 dose of Bio Farma's MR vaccine as a primary dose in infants

- To assess the safety of Bio Farma's Measles/Rubella (MR) vaccine in infants

- To evaluate immunogenicity and safety one dose of Bio Farma's MR vaccine compare to registered MR vaccine.

- To evaluate immunogenicity and safety in three consecutive batches of Bio Farma's MR vaccine in infants . ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04183114
Study type Interventional
Source PT Bio Farma
Contact
Status Completed
Phase Phase 2/Phase 3
Start date September 3, 2019
Completion date November 11, 2019

See also
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