drugset / Trial / NCT04618939
To Evaluate the Immunogenicity and Safety of 'BR-TD-1001' Administered Intramuscularly in Healthy Children
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | BR-TD-1001 | Vaccine | 0.5 ml | Intramuscular |
| Comparator | Td-pur | Vaccine | 0.5 ml | Intramuscular |