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NCT04225260 · ClinicalTrials.gov registry record · Phase 3

Long-term Treatment of Moderate to Severe Glabellar Lines and Lateral Canthal Lines

A Phase 3 study, sponsored by Galderma R&D.

Completed
Registry status
Phase 3
Development phase
902
Enrollment target

NCT04225260: Completed Phase 3 study, sponsored by Galderma R&D.

NCT04225260 is a Phase 3 study that has completed, run by Galderma R&D. The registered enrollment target is 902 participants, above the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (17% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04225260, a Phase 3 study, has completed, sponsored by Galderma R&D.

COMPLETED
Registry status
Phase 3
Development phase
902 participants
Enrollment target

Study Summary

This is a phase 3, multicenter, open-label study to evaluate the safety of QM1114-DP for the long term treatment of moderate to severe Glabellar (Frown) Lines (GL) and Lateral Canthal Lines (Crow's Feet and LCL).

Primary Outcome

4-point scale

Interventions

  • BIOLOGICAL botulinum toxin neuromodulator

Trial Details

FieldValue
Enrollment Target 902 participants
Start Date 2020-01-27
Est. Completion 2021-05-21
Phase Phase 3
Galderma R&D

158 total trials

What the finished NCT04225260 record still lists

NCT04225260 is an interventional study that assigns participants to a tested intervention. The registered 902 participants enrollment target is mid-sized for trials with a published cap, above the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (17% higher).

The record links to 0 conditions, and to 1 intervention - of which botulinum toxin neuromodulator is the first listed.

NCT04225260 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04225260 about?

NCT04225260 is a clinical study titled "Long-term Treatment of Moderate to Severe Glabellar Lines and Lateral Canthal Lines". This is a phase 3, multicenter, open-label study to evaluate the safety of QM1114-DP for the long term treatment of moderate to severe Glabellar (Frown) Lines (GL) and Lateral Canthal Lines (Crow's Feet and LCL).

What is the current status of trial NCT04225260?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 902 participants. The study started on 2020-01-27. Estimated completion is 2021-05-21.

What interventions are being tested in trial NCT04225260?

The interventions under investigation include: botulinum toxin neuromodulator (BIOLOGICAL).

Who is sponsoring clinical trial NCT04225260?

This trial is sponsored by Galderma R&D, which has 158 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04225260's enrollment target sits among peer trials

902 349th of 2000 higher than 1,652 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

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Source: ClinicalTrials.gov NCT04225260, the US trial registry maintained by the National Library of Medicine. NCT04225260 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.