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COMPLETED Phase 2

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

NCT04259086 · View on ClinicalTrials.gov ↗

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

9 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04259086

The ClinicalTrials.gov registry entry for NCT04259086 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. 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 9 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT04259086 reports 8 study locations spanning 6 distinct geographic areas — top geographies include California, Florida, Massachusetts. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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). These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04259086?

The interventions under investigation include: DaxibotulinumtoxinA for injection (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04259086?

This trial is sponsored by Revance Therapeutics, which has 9 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

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