Trials / Completed
CompletedNCT01124565
Safety Study of Two Repeat Doses of RT001 for the Treatment of Moderate to Severe Lateral Canthal Lines in Adults
A Phase 2, Open-Label, Repeat Dose, Multi-Center Study to Evaluate the Safety of RT001 Topical Gel for the Treatment of Moderate to Severe Lateral Canthal Lines in Adults
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 40 (actual)
- Sponsor
- Revance Therapeutics, Inc. · Industry
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Accepted
Summary
This study's objective is to evaluate if RT001 is safe and well-tolerated following two (2) sequential applications.
Detailed description
Revance is conducting this Phase 2 clinical study to establish the safety of two (2) sequential doses of RT001 Topical Gel at Baseline (Day 0) and Week 4 for the treatment of moderate to severe LCLs at rest.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | RT001 | RT001 (Botulinum Toxin Type A Topical Gel, Dose A) at Baseline (Day 0) and Week 4 to the lateral canthal areas |
Timeline
- Start date
- 2010-05-01
- Primary completion
- 2010-07-01
- Completion
- 2010-07-01
- First posted
- 2010-05-17
- Last updated
- 2014-01-17
Locations
3 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT01124565. Inclusion in this directory is not an endorsement.