Lateral Canthal Lines Clinical Trial
This study will evaluate the safety and efficacy of BOTOX® (botulinum toxin Type A) compared with placebo in patients with moderate to severe crow's feet lines (lateral canthal lines).
n/a
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
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Completed |
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Completed |
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Phase 2 | |
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Phase 3 | |
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Phase 2 | |
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Phase 2 | |
Completed |
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Phase 2 | |
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Phase 2 | |
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Phase 3 | |
Completed |
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Phase 2 | |
Completed |
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Phase 2 | |
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Phase 3 |