Condition: Glabellar Frown Lines · Sponsor: Revance Therapeutics, Inc.
This is a Phase 2a open-label, single-arm study to evaluate the effects of DaxibotulinumtoxinA-lanm (DAXI) for Injection on the treatment of dynamic forehead lines (FHL) and glabellar lines (GL). Approximately 40 subjects (18 years of age and above) with moderate to severe GL and FHL (all assessed at maximum contraction) will be screened for eligibility with the goal of enrolling and treating 30 subjects to receive DAXI for injection after providing informed consent. The primary objective of this study is to determine the efficacy and safety of the combined treatment of two upper facial regions with DAXI for injection.
This description comes directly from the study's public registry record.
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| Revance | Nashville, Tennessee, United States | — |
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Source record: clinicaltrials.gov/study/NCT06411002