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Clinical Trial Summary

The aim of this study is to evaluate the safety profile of Diphtheria Antitoxin


Clinical Trial Description

To assess the occurrence of serum sickness after Diphtheria Antitoxin administration. To assess local and systemic reactions within 24 hours to 10 days. To assess the occurrence of positive reactions after the sensitivity test (skin test). To assess the presence of SAE after Diphtheria Antitoxin administration. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06053853
Study type Interventional
Source PT Bio Farma
Contact
Status Completed
Phase Phase 4
Start date January 31, 2023
Completion date May 23, 2023

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