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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03912805
Other study ID # ET-01-LCL-209
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date February 27, 2019
Est. completion date October 4, 2019

Study information

Verified date July 2022
Source Eirion Therapeutics Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study tests an investigational drug formulation called ET-01, botulinum toxin, Type A, topical, in lateral canthal lines (LCL).


Description:

This product is being tested for its ability to reduce lateral canthal lines (LCL), also known as Crow's Feet.


Recruitment information / eligibility

Status Completed
Enrollment 38
Est. completion date October 4, 2019
Est. primary completion date May 6, 2019
Accepts healthy volunteers No
Gender Female
Age group 25 Years to 65 Years
Eligibility Inclusion Criteria: - females 25 - 65 years of age - minimal to moderate Crow's Feet wrinkles at rest - moderate to severe Crow's Feet on contraction - adequate vision to assess facial wrinkles in a mirror - willingness to refrain from products affecting skin remodeling - female subjects must be not pregnant and non-lactating - subjects should be in good general health Exclusion Criteria: - history of adverse reactions to any prior botulinum toxin treatments - history of vaccination or non-response to any prior botulinum toxin treatments - botulinum toxin treatment in the prior 6 months - present or history of neuromuscular disease, eyelid ptosis, muscle weakness, paralysis, or "dry eye" - history of peri-ocular surgery, brow lift or related procedures - procedures affecting the lateral canthal region in the prior 12 months - application of topical prescription medication to the treatment area - female subjects who are pregnant or are nursing a child

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
botulinum toxin, Type A
topical liniment
Vehicle
Vehicle Formulation

Locations

Country Name City State
United States Virginia Clinical Research, Inc. Norfolk Virginia
United States Synexis, Inc. Pinellas Park Florida
United States Yardley Dermatology Associates Yardley Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
Eirion Therapeutics Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Participants With a Response Defined as Change in IGA-C (Investigators Global Assessment) Score by at Least 2 Ordinals From Baseline to Week 4 Investigators Global Assessment of the Crow's Feet Wrinkle Scale where severity is scored between 0-4 (0=absent; 4=severe). Response is defined as change by at least two ordinals from Baseline to Week 4. Week 4
Secondary Total Number of Observations With a Response Defined as Change =2 in IGA-C and SSA-C Score at Any Post Baseline Visit Total number of observations with a change in the Investigators Global Assessment on Contraction, IGA-C, and the Subject Self-Assessment on Contraction, SSA-C, using the Crow's Feet Wrinkle Scale, where severity is scored between 0-4 (0=absent; 4=severe). To count, a "responder" is defined as a change by at least two ordinals in both assessments. The observation period includes all post-baseline visits from Week 1 to Week 26. Week 1, 2, 4, 8,12,18, and 26
Secondary Total Number of Observations With a Response Defined as Change in SSA-C Score = 2 at Any Post Baseline Visit Total number of observations with a change in the Subject Self-Assessment on Contraction, SSA-C, using the Crow's Feet Wrinkle Scale, where severity is scored between 0-4 (0=absent; 4=severe). To count, a "responder" is defined as a change by at least two ordinals in both assessments. The observation period includes all post-baseline visits from Week 1 to Week 26. Week 1, 2, 4, 8,12,18, and 26
See also
  Status Clinical Trial Phase
Completed NCT01951742 - Dose Finding Study In Subjects With Crow's Feet Phase 2
Completed NCT03326856 - ET-01 in Subjects With Lateral Canthal Lines Phase 2
Completed NCT03839693 - ET-01 in Subjects With Lateral Canthal Lines, LCL-208 Phase 2
Completed NCT00888914 - Safety and Efficacy Study of RT001 to Treat Moderate to Severe Lateral Canthal Lines Phase 2
Active, not recruiting NCT06021418 - Efficacy and Safety of DKB-119 in Patients in Crow's Feet N/A
Completed NCT01358695 - Clinical Trial To Evaluate ANT-1207 In Subjects With Crow's Feet Phase 2
Completed NCT01124565 - Safety Study of Two Repeat Doses of RT001 for the Treatment of Moderate to Severe Lateral Canthal Lines in Adults Phase 2
Completed NCT00968825 - Safety and Efficacy Study of RT001 to Treat Moderate to Severe Lateral Canthal Lines Phase 2
Recruiting NCT04818203 - A Study on the Anti-Wrinkle Efficacy Assessment and Safety Evaluation of the Cluster of Autologous Dermal Fibroblast on Bilateral Crow's Feet Phase 1/Phase 2
Active, not recruiting NCT04985916 - ET-01 in Subjects With Lateral Canthal Lines, LCL-210 Phase 2
Completed NCT01064518 - Efficacy and Safety Study of RT001 for the Treatment of Moderate to Severe Lateral Canthal Lines in Adults Phase 2
Completed NCT00968942 - Efficacy and Safety Study of RT001 to Treat Moderate to Severe Lateral Canthal Lines Phase 2
Completed NCT03655691 - ET-01 in Subjects With Lateral Canthal Lines, LCL-207 Phase 2
Completed NCT01124552 - A 4-Arm Efficacy and Safety Study of RT001 for the Treatment of Moderate to Severe Lateral Canthal Lines in Adults Phase 2