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Clinical Trial Summary

This is a phase 1/2, multicenter, randomized, double-blind, active-controlled and placebo-controlled study to evaluate safety,immunogenicity and efficacy of YY001 for the treatment of moderate to severe glabellar lines in male and female subjects of Chinese origin. The study has been designed to test the safety,efficacy,immunogenicity of YY001,and compare to onabotulinumtoxinA (BOTOX®) and placebo, in improving the appearance of moderate to severe glabellar lines.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Moderate to Severe Glabellar Lines

NCT number NCT05743634
Study type Interventional
Source Chongqing Claruvis Pharmaceutical Co., Ltd.
Contact
Status Completed
Phase Phase 1/Phase 2
Start date March 22, 2022
Completion date February 13, 2023

See also
  Status Clinical Trial Phase
Completed NCT05463965 - A Study to Evaluate the Efficacy and Safety of QM1114-DP for the Treatment of Moderate to Severe Glabellar Lines Phase 3
Completed NCT06151561 - Study of AGN-151586 in Japanese Participants With Moderate to Severe Glabellar Lines Phase 1
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