drugset / Trial / NCT02292472

Medytoxin® Treatment in Patients With Benign Masseteric Hypertrophy

NCT02292472 ↗

Phase 2 Completed 69 enrolled Medy-Tox
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study design is A Randomized, Double-blind, Multi-center, Phase II Optimal Dose-finding Study to Determine the Safety and Efficacy of Meditoxin® in Subjects in Benign Masseteric Hypertrophy.

Timeline

Start
2014-10-06
Primary completion
2015-05-24
Completion
2015-08-24

Drugs

EvaluationDrugModalityDoseRoute
Subject Botulinum toxin type A Protein / enzyme biologic — Intramuscular