Status:
COMPLETED
The Efficacy and Safety Study of Protoxin Versus Botox® in Subjects With Moderate to Severe Glabellar Lines
Lead Sponsor:
Protox Inc.
Conditions:
Glabellar Frown Lines
Eligibility:
All Genders
19-65 years
Phase:
PHASE3
Brief Summary
This study will be conducted in Phase Ⅲ clinical trials. In Phase Ⅲ, subjects with moderate to severe glabellar lines are enrolled and those who are judged to be eligible for this study will be inject...
Eligibility Criteria
Inclusion
- Inclusion Criteria:
- Men and women aged between 19 to 65 years old
- Subjects attaining ≥grade 2 (moderate) in the investigator's rating of the severity of glabella lines at maximum frown
- Those who understand and comply with clinical trial procedures and visit schedules
- Subjects who voluntarily decides to participate and signs the consent form after hearing the explanation of this clinical trial.
- Exclusion Criteria
- Those with or accompanied by the following diseases at the time of screening
- Subjects with Neuromuscular Junction Disorder that may affect neuromuscular action
- Subjects with previous history of weakness or paralysis in the forehead area
- Subjects with infection, skin disorders, or scars at the glabellar region
- Subjects with wrinkles that physically prevent wrinkles from spreading, such as when wrinkles are not spread out by hand
- Subjects who is administering a drug with muscle relaxation within four weeks of screening.
- Subjects who have taken Aspirin and NSAIDs within 7 days prior to administration of the investigational drug
- Subjects with surgical history who may affect wrinkles around the forehead or glabellar region
- Subjects who have planned facial cosmetic procedure during the clinical trial
- Subjects who have been administered similar drugs within 12 weeks (Botulinum toxin type A) or within 16 weeks (Botulinum toxin type B) before screening
- Subjects who are expected to administer botulinum toxin preparations other than Investigational product during the clinical trial period
- Subjects with allergy or hypersensitivity to the botulinum toxin or their components
- A history of drug or alcohol abuse
- Anxiety disorders or other significant mental disorders based on the judgment of an investigator
- Fertile women and men who have plans to conceive during pregnancy, breastfeeding and clinical trials or who do not agree to appropriate contraception
- Pregnant or lactating women
- Subjects with severe comorbidities or acute diseases that does not suitable for participation in clinical trials
- Those who participated in other clinical trials/clinical medical device trials within 30 days prior to screening and who received Investigational product/medical devices/procedures, or those who had less than 5 times the half-life of the Investigational product
- Subjects who are not eligible for this study based on the judgment of an investigator
Exclusion
Key Trial Info
Start Date :
March 6 2023
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 6 2023
Estimated Enrollment :
269 Patients enrolled
Trial Details
Trial ID
NCT05364580
Start Date
March 6 2023
End Date
October 6 2023
Last Update
November 18 2023
Active Locations (5)
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1
Kyung Hee University Hospital
Seoul, Dongdaemun-gu, South Korea
2
Chung-Ang University Hospital
Seoul, Gwangjin-gu, South Korea
3
Konkuk University Hospital
Seoul, Gwangjin-gu, South Korea
4
Nowon Eulji Medical Center
Seoul, Nowon-gu, South Korea