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Clinical Trial Summary

The objective of this study is to demonstrate the efficacy of Dysport for the improvement in appearance of moderate to severe glabellar lines and to assess the short term and long term safety of Dysport, used for the improvement in appearance of moderate to severe glabellar lines in Chinese subjects.


Clinical Trial Description

The first treatment cycle will be double blind and subjects will be randomised to receive Dysport, Botox or placebo. After the first treatment cycle, all subjects will receive a maximum of four treatment cycles with Dysport, occurring at intervals of no less than 84 Days (12 weeks) between each treatment cycle, depending upon individual duration of response to Dysport treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02450526
Study type Interventional
Source Ipsen
Contact
Status Completed
Phase Phase 3
Start date April 2015
Completion date September 6, 2017

See also
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