Expired Study
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Coral Gables, Florida 33146


Purpose:

This is a safety and efficacy study of botulinum toxin type A in subjects with lateral canthal lines.


Criteria:

Inclusion Criteria: - In good general health - Moderate to severe lateral canthal lines when evaluated at rest based on the investigator's global assessment - Moderate to severe lateral canthal lines when evaluated at rest based on the patient assessment of severity Exclusion Criteria: - Any neurological condition that may place the subject at increased risk with exposure to botulinum toxin type A such as amyotrophic lateral sclerosis and motor neuropathy, Lambert-Eaton syndrome, and myasthenia gravis - Muscle weakness or paralysis, particularly in the area receiving study treatment - Active skin disease or irritation or disrupted barrier at the treatment area - Active eye disease or irritation - Eyelid ptosis, excessive dermatochalasis, deep dermal scarring, or inability to substantially effect the LCL to be treated by manually spreading the skin apart - Use of topical prescription retinoid product(s) in the lateral canthal areas during the 3 months prior to Screening - Undergone any procedures that may affect the lateral canthal region during the 12 months prior to Screening - Treatment with botulinum toxin type A in the lateral canthal areas in the 6 months prior to Screening or 3 months anywhere else in the body


NCT ID:

NCT02580370


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Coral Gables, Florida 33146
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 18, 2019

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