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Randomized, Double-blind, Active-controlled, Multicenter, Phase I/III Clinical Trial to Evaluate the Safety and Efficacy of Botulax® as Compared to Botox® in Subject With Moderate to Severe Crow's Feet Lines
To determine the efficacy and safety of Botulax® in treatment of crow's feet line
1. Allocation: Randomized 2. Masking: Double Blind
Age
19 - 65 years
Sex
ALL
Healthy Volunteers
Yes
Hugel
Seoul, South Korea
Start Date
January 17, 2018
Primary Completion Date
December 13, 2018
Completion Date
June 7, 2019
Last Updated
April 15, 2022
240
ACTUAL participants
Botulinum toxin type A
DRUG
Botulinum toxin type A
DRUG
Lead Sponsor
Hugel
NCT06402058
NCT01797081
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT02176356