drugset / Trial / NCT04143815

Clinical Trial to Evaluate the Efficacy and Safety of MBA-P01 in Treatment of Glabellar Lines

NCT04143815

Phase 2 Completed 200 enrolled Medy-Tox
RandomizedParallel-groupDouble-blindTreatment

Summary

This study will determine the effect of MBA-P01 in subjects with glabellar lines at a range of doses compared with placebo. This study includes two treatment period; 1) Dose-ranging period, Day0 to 16weeks and 2) Open-label extension period, 16 weeks to 52.

Timeline

Start
2019-05-20
Primary completion
2020-09-01
Completion
2020-09-01

Drugs

EvaluationDrugModalityDoseRoute
Subject MBA-P01 Protein / enzyme biologic 10 iu Intramuscular
Subject MBA-P01 Protein / enzyme biologic 20 iu Intramuscular
Subject MBA-P01 Protein / enzyme biologic 30 iu Intramuscular

Indications

No indication recorded.