ET-01 in Subjects With Lateral Canthal Lines, LCL-207

Completed · Phase 2

Conditions studied: Lateral Canthal Lines, Crow's Feet

In brief

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

Key facts

Study ID: NCT03655691
Run by: Eirion Therapeutics Inc.
People needed: 79
Starts: 2018-08-16
Expected to finish: 2019-04-11
Last updated by the study team: 2022-04-21

Who can join

Age: 25 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

25 - 65 years of age
minimal to moderate Crow's Feet wrinkles at rest
moderate to severe Crow's Feet wrinkles on contraction
willingness to refrain from any product affecting skin remodeling
female subjects must be not pregnant and non-lactating

You may not qualify if…

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

Where it is running

Baumann Cosmetic & Research Institute — Miami, Florida, United States
Radiant Research, Inc. — Pinellas Park, Florida, United States
Research Institute of the Southeast, LLC — West Palm Beach, Florida, United States
Dermatology NOLA Inc. — Metairie, Louisiana, United States
Westlake Dermatology Clinical Research Center — Austin, Texas, United States
Virginia Clinical Research, Inc. — Norfolk, Virginia, United States

Full record on ClinicalTrials.gov

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