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NCT01776606 · ClinicalTrials.gov registry record · Phase 3

Efficacy and Safety Study of Botulinum Toxin Type A for Moderate to Severe Crow's Feet Lines

A Phase 3 study of Skin Aging, sponsored by Revance Therapeutics.

Completed
Registry status
Phase 3
Development phase
247
Enrollment target
1
Study location

NCT01776606: Completed Phase 3 study of Skin Aging, sponsored by Revance Therapeutics.

NCT01776606 is a Phase 3 study of Skin Aging that has completed, run by Revance Therapeutics. The registered enrollment target is 247 participants, above the 48-participant average among 9 other Skin Aging trials with a reported enrollment target (415% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01776606, a Phase 3 study of Skin Aging, has completed, sponsored by Revance Therapeutics.

COMPLETED
Registry status
Phase 3
Development phase
247 participants
Enrollment target
1
Study location

Study Summary

This study will evaluate the efficacy and safety of botulinum toxin type A compared to placebo control for the treatment of moderate to severe crow's feet lines.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG Botulinum Toxin Type A

Study Locations (1)

Florida

  • Dermatology Research Institute - Coral Gables

Trial Details

FieldValue
Enrollment Target 247 participants
Start Date 2012-12
Est. Completion 2013-05
Phase Phase 3
Revance Therapeutics

27 total trials

What the finished NCT01776606 record still lists

NCT01776606 is an interventional study that assigns participants to a tested intervention. The registered 247 participants enrollment target is mid-sized for trials with a published cap, above the 48-participant average among 9 other Skin Aging trials with a reported enrollment target (415% higher).

The record links to 1 condition, with Skin Aging appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT01776606 reports a single indexed study location in Florida.

Frequently Asked Questions

What is clinical trial NCT01776606 about?

NCT01776606 is a clinical study titled "Efficacy and Safety Study of Botulinum Toxin Type A for Moderate to Severe Crow's Feet Lines". This study will evaluate the efficacy and safety of botulinum toxin type A compared to placebo control for the treatment of moderate to severe crow's feet lines.

What is the current status of trial NCT01776606?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 247 participants. The study started on 2012-12. Estimated completion is 2013-05.

What conditions does trial NCT01776606 study?

This clinical trial studies the following conditions: Skin Aging.

What interventions are being tested in trial NCT01776606?

The interventions under investigation include: Placebo (DRUG), Botulinum Toxin Type A (DRUG).

Who is sponsoring clinical trial NCT01776606?

This trial is sponsored by Revance Therapeutics, which has 27 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01776606 being conducted?

This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Skin Aging

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT01776606's enrollment target sits among peer trials

247 1st of 9 higher than 9 of 9 other Skin Aging trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Skin Aging trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01776606, the US trial registry maintained by the National Library of Medicine. NCT01776606 (mid enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.