ET-01 in Subjects With Lateral Canthal Lines, LCL-208



Status:Recruiting
Healthy:No
Age Range:25 - 65
Updated:2/17/2019
Start Date:October 16, 2018
End Date:August 2019

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Clinical Trial to Evaluate ET-01 in Subjects With Lateral Canthal Lines

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

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

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
We found this trial at
5
sites
Miami, Florida 33140
Phone: 305-531-5788
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Austin, Texas 78746
Phone: 512-615-3193
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Austin, TX
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Louisville, Kentucky 40202
Phone: 502-434-4181
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Louisville, KY
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Norfolk, Virginia 23507
Phone: 757-625-0151
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Norfolk, VA
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Pinellas Park, Florida 33781
Phone: 513-247-5520
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Pinellas Park, FL
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