Clinical Trials Directory

Trials / Completed

CompletedNCT01064518

Efficacy and Safety Study of RT001 for the Treatment of Moderate to Severe Lateral Canthal Lines in Adults

A Phase 2, Double-Blind, Randomized, Parallel-Group, Controlled, Multi-Center Study to Evaluate the Efficacy and Safety of RT001, a Botulinum Toxin Type A Topical Gel, for the Treatment of Moderate to Severe Lateral Canthal Lines in Adults

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
90 (actual)
Sponsor
Revance Therapeutics, Inc. · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to find out if an investigational drug, called RT001 Botulinum Toxin Type A Topical Gel, is safe and useful in minimizing the wrinkles between the eye and hairline called crow's feet, also known as lateral canthal lines.

Detailed description

RT001, a new drug, may be effective for the temporary improvement in the appearance of moderate to severe lateral canthal lines (crow's feet wrinkles) in adults. In this study, researchers want to find out if RT001is more effective than placebo gel by examining the effect on the improvement of crow's feet by both the patient and physician.

Conditions

Interventions

TypeNameDescription
DRUGBotulinum Toxin Type ART001 (Botulinum Toxin Type A Topical Gel, Dose A) applied topically at Baseline (Day 0) to the lateral canthal lines
DRUGPlacebo (Dose B)Placebo (Dose B), applied topically at Baseline (Day 0) to the lateral canthal lines

Timeline

Start date
2010-01-01
Primary completion
2010-07-01
Completion
2010-07-01
First posted
2010-02-08
Last updated
2020-08-28

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01064518. Inclusion in this directory is not an endorsement.