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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 glabellar lines.


Clinical Trial Description

The allocated subject is injected Investigational Product(Meditoxin® or Botox®) 20U in middle of the forehead. The efficacy and safety are evaluated for 16weeks through 4 follow up visits. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01237977
Study type Interventional
Source Medy-Tox
Contact
Status Completed
Phase Phase 3
Start date November 23, 2009
Completion date September 30, 2010

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