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NCT04259086 · ClinicalTrials.gov registry record · Phase 2

Efficacy and Safety of DaxibotulinumtoxinA (DAXI) for Injection for Treatment of Upper Facial Lines

A Phase 2 study of Upper Facial Lines (Glabellar Lines, Forehead Lines, & Lateral Canthal Lines), sponsored by Revance Therapeutics.

Completed
Registry status
Phase 2
Development phase
48
Enrollment target
8
Study locations

NCT04259086 is a Phase 2 study of Upper Facial Lines (Glabellar Lines, Forehead Lines, & Lateral Canthal Lines) that has completed, run by Revance Therapeutics. The registered enrollment target is 48 participants. The trial reports 8 study locations across 6 states.

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The verdict

NCT04259086, a Phase 2 study of Upper Facial Lines (Glabellar Lines, Forehead Lines, & Lateral Canthal Lines), has completed, sponsored by Revance Therapeutics.

COMPLETED
Registry status
Phase 2
Development phase
48 participants
Enrollment target
8
Study locations

Study Summary

This is a Phase 2, multicenter, open-label, single-arm study to evaluate the efficacy and safety of DaxibotulinumtoxinA for injection (DAXI for injection) in the treatment of Glabellar Lines (GL), Dynamic Forehead Lines (FHL), and Lateral Canthal Lines(LCL)

Interventions

  • DRUG DaxibotulinumtoxinA for injection

Study Locations (8)

California

  • Site 1 - Manhattan Beach
  • Site 3 - San Diego
  • Site 7 - Santa Monica

Florida

  • Site 5 - Coral Gables

Massachusetts

  • Site 2 - Chestnut Hill

New York

  • Site 6 - New York

British Columbia

  • Site 4 - Vancouver

Ontario

  • Site 8 - Toronto

Trial Details

FieldValue
Enrollment Target 48 participants
Start Date 2019-12-06
Est. Completion 2020-11-02
Phase Phase 2

Sponsor

Revance Therapeutics

27 total trials

What the Registry Record Tells You About NCT04259086

The ClinicalTrials.gov registry entry for NCT04259086 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 48 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Revance Therapeutics, which has 27 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Upper Facial Lines (Glabellar Lines, Forehead Lines, & Lateral Canthal Lines) appearing as the primary indexed condition, and to 1 intervention - of which DaxibotulinumtoxinA for injection is the first listed.

NCT04259086 reports 8 study locations spanning 6 distinct geographic areas - top geographies include California, Florida, Massachusetts.

Frequently Asked Questions

What is clinical trial NCT04259086 about?

NCT04259086 is a clinical study titled "Efficacy and Safety of DaxibotulinumtoxinA (DAXI) for Injection for Treatment of Upper Facial Lines". This is a Phase 2, multicenter, open-label, single-arm study to evaluate the efficacy and safety of DaxibotulinumtoxinA for injection (DAXI for injection) in the treatment of Glabellar Lines (GL), Dynamic Forehead Lines (FHL), and Lateral Canthal Lines(LCL)

What is the current status of trial NCT04259086?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 48 participants. The study started on 2019-12-06. Estimated completion is 2020-11-02.

What conditions does trial NCT04259086 study?

This clinical trial studies the following conditions: Upper Facial Lines (Glabellar Lines, Forehead Lines, & Lateral Canthal Lines).

What interventions are being tested in trial NCT04259086?

The interventions under investigation include: DaxibotulinumtoxinA for injection (DRUG).

Who is sponsoring clinical trial NCT04259086?

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

Where is trial NCT04259086 being conducted?

This trial has 8 study locations across California, Florida, Massachusetts, New York, British Columbia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.