Overview
This study is A Randomized, Double-blind, Placebo-controlled, Multi-center Phase II Optimal Dose-finding Study to Evaluate the Safety and Efficacy of Botulax in Subjects with Benign Masseteric Hypertrophy
Description
A Randomized, Double-blind, Placebo-controlled, Multi-center Phase Optimal Dose-finding Study to Evaluate the Safety and Efficacy of Botulax in Subjects with Benign Masseteric Hypertrophy
Eligibility
Inclusion Criteria:
- Male and Female adults aged 19 or older.
- Sighting, facilitation measurement are judged by the investigator to be the ratio of Benign Masseteric Hypertrophy.
- Subject who understand and willing to perform with the procedures and visiting schedules of clinical trial.
- Subject who voluntarily agree to participate in this clinical trial.
Exclusion Criteria:
- Subject who is clinically significant facial asymmetry in visual measurement by the investigator.
- Fertile women and men who have plans to conceive during pregnancy, breastfeeding and clinical trials or who do not agree to appropriate contraception.
- Subject who is deemed unable to participate in a clinical trial under the judgement of a Investigator.