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NCT02096081 · ClinicalTrials.gov registry record · Phase 4

The Treatment of Glabellar Frown Lines

A Phase 4 study, sponsored by Merz North America.

Completed
Registry status
Phase 4
Development phase
250
Enrollment target

NCT02096081 is a Phase 4 study that has completed, run by Merz North America. The registered enrollment target is 250 participants.

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The verdict

NCT02096081, a Phase 4 study, has completed, sponsored by Merz North America.

COMPLETED
Registry status
Phase 4
Development phase
250 participants
Enrollment target

Study Summary

The purpose of this study is to show that two FDA-approved botulinum toxin drugs called Xeomin® and Botox® can reduce the severity of vertical lines (wrinkles) that appear between the eyebrows (glabellar frown lines).

Interventions

  • DRUG OnabotulinumtoxinA
  • DRUG IncobotulinumtoxinA

Trial Details

FieldValue
Enrollment Target 250 participants
Start Date 2014-02
Est. Completion 2014-11
Phase Phase 4

Sponsor

Merz North America

35 total trials

What the Registry Record Tells You About NCT02096081

The ClinicalTrials.gov registry entry for NCT02096081 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 250 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Merz North America, which has 35 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which OnabotulinumtoxinA is the first listed.

NCT02096081 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02096081 about?

NCT02096081 is a clinical study titled "The Treatment of Glabellar Frown Lines". The purpose of this study is to show that two FDA-approved botulinum toxin drugs called Xeomin® and Botox® can reduce the severity of vertical lines (wrinkles) that appear between the eyebrows (glabellar frown lines).

What is the current status of trial NCT02096081?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 250 participants. The study started on 2014-02. Estimated completion is 2014-11.

What interventions are being tested in trial NCT02096081?

The interventions under investigation include: OnabotulinumtoxinA (DRUG), IncobotulinumtoxinA (DRUG).

Who is sponsoring clinical trial NCT02096081?

This trial is sponsored by Merz North America, which has 35 total clinical trials registered on ClinicalTrials.gov.

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.