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Clinical Trial Summary

The objective of this study was to achieve the post-marketing protective effect research of Speeda® rabies vaccine for human use from Chengda Bio.


Clinical Trial Description

When found the injury who is bitten by the animal to three-level, the investigators would enroll the participant after explaining the protection and making him signed the informed consent. The patient would inject rabies vaccine as follow the national regulation, meanwhile the investigators would get the blood samples to detect whether the man-killer carries the rabies virus. ;


Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT01827917
Study type Interventional
Source Beijing Center for Disease Control and Prevention
Contact
Status Completed
Phase Phase 4
Start date February 2013
Completion date December 2014

See also
  Status Clinical Trial Phase
Completed NCT01821911 - The Post-Marketing Safety and Immunogenicity Research of Speeda® Rabies Vaccine for Human Use Phase 4