# A 4-Arm Efficacy and Safety Study of RT001 for the Treatment of Moderate to Severe Lateral Canthal Lines in Adults

> **NCT01124552** · PHASE2 · COMPLETED · sponsor: **Revance Therapeutics, Inc.** · enrollment: 180 (actual)

## Conditions studied

- Lateral Canthal Lines
- Crow's Feet
- Facial Wrinkles

## Interventions

- **DRUG:** RT001 Botulinum toxin type A (Dose A)
- **DRUG:** RT001 Botulinum Toxin Type A (Dose B)
- **OTHER:** Vehicle
- **DRUG:** Placebo

## Key facts

- **NCT ID:** NCT01124552
- **Lead sponsor:** Revance Therapeutics, Inc.
- **Sponsor class:** INDUSTRY
- **Phase:** PHASE2
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2010-04
- **Primary completion:** 2010-07
- **Final completion:** 2010-07
- **Target enrollment:** 180 (ACTUAL)
- **Last updated:** 2014-01-30


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01124552

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01124552, "A 4-Arm Efficacy and Safety Study of RT001 for the Treatment of Moderate to Severe Lateral Canthal Lines in Adults". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT01124552. Licensed CC0.

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