drugset / Trial / NCT04618939

To Evaluate the Immunogenicity and Safety of 'BR-TD-1001' Administered Intramuscularly in Healthy Children

NCT04618939

Phase 3 Completed 218 enrolled Boryung Biopharma Co., Ltd.
RandomizedParallel-groupDouble-blindPrevention

Summary

The purpose of this study is to evaluate immunogenicity by measuring the seroprotection rate against diphtheria and tetanus at 28 days after vaccination with BR-TD-1001 and Td-pur-inj.

Timeline

Start
2016-10-20
Primary completion
2017-04-28
Completion
2017-04-28

Drugs

EvaluationDrugModalityDoseRoute
Subject BR-TD-1001 Vaccine 0.5 ml Intramuscular
Comparator Td-pur Vaccine 0.5 ml Intramuscular

Indications