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Clinical Trial Summary

This is a phase 3, multicenter, randomized, double-blind, active-controlled and placebo-controlled study to evaluate the efficacy and safety of 50 units (U) of QM1114-DP for the treatment of moderate to severe GL in male and female subjects of Chinese origin. The study has been designed to test the superiority of QM1114-DP compared to placebo, and the non-inferior efficacy of QM1114-DP compared to onabotulinumtoxinA (BOTOX®), in improving the appearance of moderate to severe GL.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Moderate to Severe Glabellar Lines

NCT number NCT05463965
Study type Interventional
Source Galderma R&D
Contact
Status Completed
Phase Phase 3
Start date July 29, 2022
Completion date June 15, 2023

See also
  Status Clinical Trial Phase
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Completed NCT02353871 - Efficacy and Safety of Clostridium Botulinum Toxin Type A to Improve Appearance of Moderate to Severe Glabellar Lines Phase 3
Recruiting NCT06199336 - A Phase I/II, Randomized, Double-blind, Placebo, and Active Controlled Clinical Study to Evaluate the Safety, Tolerability, Immunogenicity, and Preliminary Efficacy of JHM03 in Subjects With Moderate to Severe Glabellar Lines Phase 1/Phase 2
Completed NCT06354127 - DWP450 for Treating Moderate to Severe Glabellar Lines Phase 3
Completed NCT03970876 - Safety and Efficacy Study of ATGC-100 for the Treatment of Moderate to Severe Glabellar Lines in Adult Subjects Phase 1/Phase 2