drugset / Trial / NCT04249687

Treatment of Moderate to Severe Lateral Canthal Lines

NCT04249687

Phase 3 Completed 303 enrolled Galderma R&D
RandomizedParallel-groupQuadruple-blindTreatment

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.

Timeline

Start
2020-02-10
Primary completion
2020-09-25
Completion
2021-02-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Botulinum toxin Protein / enzyme biologic Intramuscular

Indications