Lateral Canthal Lines
Conditions
Keywords
Lateral Canthal Lines, Crow's Feet, Facial Wrinkles
Brief summary
The purpose of this study is to evaluate the safety and efficacy of RT001 to treat moderate to severe lateral canthal lines in adults and duration of effect.
Detailed description
This is a double-blind, randomized, parallel-group, controlled, dose-ranging, multi-center study to evaluate the safety and efficacy of RT001 compared to placebo applied as a single, bilateral application in at least 180 subjects with moderate to severe LCLs. Subjects will be randomized within each site to 1 of 3 treatment groups in a 1:1:1 ratio. The safety and efficacy of two different doses of RT001, compared to placebo, will be evaluated. At least 180 adult volunteers who have provided informed consent and have met the study eligibility criteria will be enrolled. Subjects will be enrolled in two (2) sequential cohorts. Cohort 1 will consist of 72 subjects; 24 subjects per treatment group. Cohort 2 will consist of 108 subjects; 36 subjects per treatment group. In order to confirm the safety of the test articles, Cohort 2 will not be enrolled until all Cohort 1 subjects have reached Day 14 or later with no Study Pause Criteria being observed.
Interventions
DRUGRT001
Dose A RT001
OTHERPlacebo
Dose C Placebo
Sponsors
Revance Therapeutics, Inc.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
30 Years to 60 Years
Healthy volunteers
Yes
Inclusion criteria
* Female or male, 30 to 60 years of age * Bilateral lateral canthal lines rated as moderate or severe * Willing to refrain from receiving facial fillers, laser treatments, use of any product that affects skin remodeling or a product that may cause an active dermal response in the treatment area beginning at Screening and through End of Study * Women of childbearing potential must be practicing and willing to continue to use an effective method of birth control during the course of the study
Exclusion criteria
* Muscle weakness or paralysis in the area receiving study treatment -Active skin disease or irritation at the treatment areas * Undergone any procedures that may affect the lateral canthal region during the past 12 months prior to Screening * Use of a topical steroid on either of the treatment areas or use of medications that suppress the immune system 30 days prior to Screening and continuing through End of Study (Day 28) * Any abnormality on the electrocardiogram (ECG) at Screening or any history of clinically significant arrhythmia, unstable angina, myocardial infarction or congestive heart failure. * Previous treatment with Botulinum Toxin Type A in the face area
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The number of subjects classified as exhibiting improvement via the Investigator Global Assessment at Rest from Baseline (Day 0) to Day 28 | Day 28 |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of treatment-emergent adverse events | Day 28 |
Countries
United States
Outcome results
None listed