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Clinical Trial Summary

This is a blinded, randomized study in the US to compare the duration response of two different concentrations of BOTOX in healthy female subjects with moderate to severe dynamic glabellar lines on maximum frown.


Clinical Trial Description

This study involves a blinded, randomized, parallel-group design. The aim of this study is to evaluate the duration response of BOTOX in subjects with moderate to severe dynamic glabellar lines at the approved on-label dose of 20 U, however comparing the use of highly Concentrated On Label Dose (COLD) to the On Label Dose and concentration (OLD). The COLD concentration is defined as 4 Units per 0.02 mL and the OLD concentration is defined as 4 Units per 0.1 mL. The total BOTOX dose will be 20U divided into 5 injections for both study groups. However, the injection volume will differ for the two study groups, such that the OLD (4 U per 0.1 mL) group will receive a total of 0.5 mL and the COLD (4 U per 0.02 mL) group will receive a total of 0.1mL. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05083286
Study type Interventional
Source Clinical Testing of Beverly Hills
Contact Mary Hayes
Phone 747-998-5160
Email mary@clinicaltestingcenter.com
Status Recruiting
Phase Early Phase 1
Start date October 20, 2021
Completion date August 1, 2022

See also
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