drugset / Trial / NCT05059587

Study to Evaluate the Efficacy and Safety of MBA-P01 in Subjects With Glabellar Lines

NCT05059587

Phase 3 Completed 318 enrolled Medytox Korea
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study is intended to evaluate the efficacy and safety of MBA-P01 compared to BOTOX in treatment of glabellar lines.

Timeline

Start
2021-08-30
Primary completion
2021-12-29
Completion
2022-03-29

Drugs

EvaluationDrugModalityDoseRoute
Comparator Botulinum toxin type A Protein / enzyme biologic Other
Subject MBA-P01 Protein / enzyme biologic Other

Indications

No indication recorded.