drugset / Trial / NCT03837561

The Efficacy and Safety of CUNOX® in Patients With Moderate to Severe Glabellar Lines

NCT03837561

Phase 3 Completed 136 enrolled Medy-Tox
RandomizedParallel-groupQuadruple-blindTreatment

Summary

To Confirm the non-inferiority of CUNOX® to BOTOX® in the glabellar line improvement of moderate to severe glabellar lines.

Timeline

Start
2018-12-13
Primary completion
2019-03-12
Completion
2019-06-03

Drugs

EvaluationDrugModalityDoseRoute
Comparator Botulinum toxin type A Protein / enzyme biologic 20 iu
Subject Cunox Unknown 20 iu

Indications

No indication recorded.