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 | |
|---|---|---|---|
| Completed |
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Safety and Effectiveness of BOTOX® for Lateral Canthal Lines With or Without Simultaneous Glabellar Lines in Korea
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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 3 | |
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N/A | |
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Phase 2 | |
| Completed |
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Phase 3 | |
| Completed |
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Phase 2 | |
| Completed |
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Phase 2 | |
| Completed |
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Phase 2 | |
| Completed |
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|
Phase 2 | |
| Completed |
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|
Phase 2 | |
| Completed |
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|
Phase 2 | |
| Completed |
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Efficacy and Safety of Increasing Doses of DaxibotulinumtoxinA for Injection (DAXI for Injection) in the Treatment of Moderate or Severe Lateral Canthal Lines
|
Phase 2 | |
| Completed |
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Safety and Efficacy Study of RT001 to Treat Moderate to Severe Lateral Canthal Lines
|
Phase 2 | |
| Completed |
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Long-term Treatment of Moderate to Severe Glabellar Lines and Lateral Canthal Lines
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Phase 3 | |
| Completed |
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Phase 2 | |
| Completed |
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Safety and Efficacy Study of RT001 to Treat Moderate to Severe Lateral Canthal Lines
|
Phase 2 | |
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|
Phase 3 |