drugset / Trial / NCT01821911

The Post-Marketing Safety and Immunogenicity Research of Speeda® Rabies Vaccine for Human Use

NCT01821911 ↗

Phase 4 Completed 10500 enrolled Beijing Center for Disease Control and Prevention
RandomizedParallel-groupOpen-labelPrevention

Summary

The objective of this study was to achieve the post-marketing safety and immunogenicity research of Speeda® rabies vaccine for human use from Chengda Bio

Timeline

Start
2012-07
Primary completion
2013-12
Completion
2014-12

Drugs

EvaluationDrugModalityDoseRoute
Subject SPEEDA Vaccine — Intramuscular