Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT03014622 · ClinicalTrials.gov registry record · Phase 3

Efficacy and Safety of DaxibotulinumtoxinA for Injection to Treat Moderate to Severe Glabellar Lines

A Phase 3 study, sponsored by Revance Therapeutics.

Completed
Registry status
Phase 3
Development phase
303
Enrollment target

NCT03014622: Completed Phase 3 study, sponsored by Revance Therapeutics.

NCT03014622 is a Phase 3 study that has completed, run by Revance Therapeutics. The registered enrollment target is 303 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (61% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03014622, a Phase 3 study, has completed, sponsored by Revance Therapeutics.

COMPLETED
Registry status
Phase 3
Development phase
303 participants
Enrollment target

Study Summary

This is a safety and efficacy study of DaxibotulinumtoxinA for Injection to treat moderate to severe frown lines.

Primary Outcome

Percentage of subjects who achieve at least a 2-point improvement from baseline and a score of 0 or 1 (i.e., none or mild wrinkles in severity) on both Investigator and Subject Frown Wrinkle Severity (FWS) assessments

Interventions

  • BIOLOGICAL Botulinum Toxins, Type A
  • BIOLOGICAL Placebos

Trial Details

FieldValue
Enrollment Target 303 participants
Start Date 2016-12-08
Est. Completion 2017-11-14
Phase Phase 3
Revance Therapeutics

27 total trials

What the finished NCT03014622 record still lists

NCT03014622 is an interventional study that assigns participants to a tested intervention. The registered 303 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (61% lower).

The record links to 0 conditions, and to 2 interventions - of which Botulinum Toxins, Type A is the first listed.

NCT03014622 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03014622 about?

NCT03014622 is a clinical study titled "Efficacy and Safety of DaxibotulinumtoxinA for Injection to Treat Moderate to Severe Glabellar Lines". This is a safety and efficacy study of DaxibotulinumtoxinA for Injection to treat moderate to severe frown lines.

What is the current status of trial NCT03014622?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 303 participants. The study started on 2016-12-08. Estimated completion is 2017-11-14.

What interventions are being tested in trial NCT03014622?

The interventions under investigation include: Botulinum Toxins, Type A (BIOLOGICAL), Placebos (BIOLOGICAL).

Who is sponsoring clinical trial NCT03014622?

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

How this trial's enrollment target compares

Where NCT03014622's enrollment target sits among peer trials

303 1119th of 2000 higher than 882 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT05508971 · 303 participants · NA

    Treatment of Obstructive Sleep Apnea With Personalized Surgery in Children With Down Syndrome (TOPS-DS)

  • NCT04750616 · 304 participants · Phase 2

    NAD+ Augmentation in Cardiac Surgery Associated Myocardial Injury Trial

  • NCT04994717 · 304 participants · Phase 3

    Study Comparing Blinatumomab Alternating With Low-intensity Chemotherapy Versus Standard of Care Chemotherapy for Older Adults With Newly Diagnosed Philadelphia-negative B-cell Precursor Acute Lymphoblastic Leukemia

  • NCT06036147 · 304 participants · NA

    Concussion Health Improvement Program

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT03014622, the US trial registry maintained by the National Library of Medicine. NCT03014622 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.