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Efficacy and Safety of MEDITOXIN® in Cervical Dystonia — CD Phase III  

Cervical Dystonia Clinical Trial

Official title:
A Prospective, Randomized, Multi-center, Phase III, Double-Blind, Activi Controlled, Parallel-group Study to Evaliate the Efficacy and Safety of MEDITOXIN® Comparison With BOTOX® in Treatment of Cervical Dystonia

Clinical Trial Summary

The purpose of this study is to test the hypothesis that the efficacy and safety of Meditoxin® are not inferior to Botox®'s in the treatment of Cervical Dystonia.

Clinical Trial Description

The allocated subject is injected Investigational Product(Meditoxin® or Botox®) 200~300U in cervical muscles. The efficacy and safety are evaluated for 12weeks through 4 follow up visits. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03905304
Study type Interventional
Source Medy-Tox
Contact
Status Completed
Phase Phase 3
Start date January 9, 2013
Completion date August 5, 2014
View Details
See also
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