Clinical Trials Directory

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

TypeNameDescription
DRUGRT001RT001 (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.

Safety Study of Two Repeat Doses of RT001 for the Treatment of Moderate to Severe Lateral Canthal Lines in Adults (NCT01124565) · Clinical Trials Directory