Clinical Trials Logo

Clinical Trial Summary

Phase I/II clinical trial will be integrated and conducted. In phase I clinical trial, subjects with moderate to severe glabellar lines at maximum frown are enrolled and safety is assessed after 12 weeks of administration of 20U of ATGC-100. In phase II clinical trial, subjects with moderate to severe glabellar lines at maximum frown are enrolled, and efficacy and safety are assessed by comparing with Botox (Allergan).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Moderate to Severe Glabellar Lines

NCT number NCT03970876
Study type Interventional
Source EuBiologics Co.,Ltd
Contact
Status Completed
Phase Phase 1/Phase 2
Start date April 19, 2019
Completion date December 23, 2019

See also
  Status Clinical Trial Phase
Completed NCT05743634 - A Phase I/II Study of Recombinant Botulinum Toxin Type A for the Treatment of Moderate to Severe Glabellar Lines Phase 1/Phase 2
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