drugset / Trial / NCT04281095

A Comparative Study of Botulinum Neurotoxin Type A in Treatment of Moderate to Severe Glabellar Frown Lines

NCT04281095

Phase 1/2 Completed 60 enrolled ATGC Co., Ltd.
RandomizedParallel-groupDouble-blindTreatment

Summary

Efficacy and safety of the investigational product, ATGC-110, was evaluated in comparison with Botox for a total of 12 weeks after the administration in treatment of glabellar frown lines.

Timeline

Start
2019-11-01
Primary completion
2020-04-30
Completion
2020-04-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Botulinum toxin type A Protein / enzyme biologic 20 iu Intramuscular

Indications

No indication recorded.