Treatment of Moderate to Severe Lateral Canthal Lines and Glabellar Lines Alone or in Combination

Completed · Phase 3 · Has a placebo group

Conditions studied: Glabellar Frown Lines (GL), Lateral Canthal Lines (LCL)

In brief

This study is designed to evaluate the safety and efficacy of a single dose of QM1114-DP for the treatment of moderate to severe LCL and moderate to severe GL, alone or in combination.

Key facts

Study ID
NCT04247074
Run by
Galderma R&D
People needed
413
Starts
2020-02-10
Expected to finish
2021-02-26
Last updated by the study team
2023-09-06

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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