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NCT04249687 · ClinicalTrials.gov registry record · Phase 3
Treatment of Moderate to Severe Lateral Canthal Lines
A Phase 3 study, sponsored by Galderma R&D.
- Completed
- Registry status
- Phase 3
- Development phase
- 303
- Enrollment target
NCT04249687: Completed Phase 3 study, sponsored by Galderma R&D.
NCT04249687 is a Phase 3 study that has completed, run by Galderma R&D. 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.
The verdict
NCT04249687, a Phase 3 study, has completed, sponsored by Galderma R&D.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 303 participants
- Enrollment target
Study Summary
The objective of the study is to evaluate the efficacy and safety of a single dose of QM1114-DP compared to placebo for the treatment of moderate to severe LCL.
Primary Outcome
The investigator and subject evaluate the subject's LCL severity using a 4-grade scale (0 = none and 3 = severe)
Interventions
- BIOLOGICAL Placebo
- BIOLOGICAL botulinum toxin
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 303 participants |
| Start Date | 2020-02-10 |
| Est. Completion | 2021-02-10 |
| Phase | Phase 3 |
What the finished NCT04249687 record still lists
NCT04249687 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 Placebo is the first listed.
NCT04249687 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT04249687 about?
NCT04249687 is a clinical study titled "Treatment of Moderate to Severe Lateral Canthal Lines". The objective of the study is to evaluate the efficacy and safety of a single dose of QM1114-DP compared to placebo for the treatment of moderate to severe LCL.
What is the current status of trial NCT04249687?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 303 participants. The study started on 2020-02-10. Estimated completion is 2021-02-10.
What interventions are being tested in trial NCT04249687?
The interventions under investigation include: Placebo (BIOLOGICAL), botulinum toxin (BIOLOGICAL).
Who is sponsoring clinical trial NCT04249687?
This trial is sponsored by Galderma R&D, which has 158 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT04249687'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
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