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Last Updated: December 22, 2024

CLINICAL TRIALS PROFILE FOR SKLICE


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All Clinical Trials for sklice

Trial ID Title Status Sponsor Phase Start Date Summary
NCT03257943 ↗ A Bioequivalence Study, Comparing Two Formulations of Ivermectin Lotion, 0.5% Completed Taro Pharmaceuticals USA Phase 1 2017-03-20 A Multi-Center, Double-Blind, Randomized, Placebo controlled, Parallel-group study, comparing Ivermectin Lotion, 0.5%
NCT03301649 ↗ Clinical Endpoint Study of Ivermectin 0.5% Lotion Completed Teva Pharmaceuticals USA Phase 3 2017-10-07 This clinical study is designed to evaluate the clinical (therapeutic) effect of a generic ivermectin lotion 0.5% (Actavis Laboratories UT, Inc.) relative to that of the Food and Drug Administration (FDA) Reference Listed Drug (RLD) SKLICEĀ® (ivermectin) lotion, 0.5% (Arbor Pharmaceuticals, LLC) in participants with active head lice infestation. Additionally, both the test and reference (that is; the RLD) treatments were tested for superiority to a placebo.
NCT03301649 ↗ Clinical Endpoint Study of Ivermectin 0.5% Lotion Completed Actavis Inc. Phase 3 2017-10-07 This clinical study is designed to evaluate the clinical (therapeutic) effect of a generic ivermectin lotion 0.5% (Actavis Laboratories UT, Inc.) relative to that of the Food and Drug Administration (FDA) Reference Listed Drug (RLD) SKLICEĀ® (ivermectin) lotion, 0.5% (Arbor Pharmaceuticals, LLC) in participants with active head lice infestation. Additionally, both the test and reference (that is; the RLD) treatments were tested for superiority to a placebo.
NCT03337490 ↗ A Clinical Endpoint Bioequivalence Study to Assess Efficacy and Safety of Ivermectin 0.5% Lotion in the Treatment of Head Lice Completed bioRASI, LLC Phase 3 2017-10-02 This is a phase 3 randomized, multi-center, double-blind, placebo controlled, parallel group design study.
NCT03337490 ↗ A Clinical Endpoint Bioequivalence Study to Assess Efficacy and Safety of Ivermectin 0.5% Lotion in the Treatment of Head Lice Completed Mayne Pharma International Pty Ltd Phase 3 2017-10-02 This is a phase 3 randomized, multi-center, double-blind, placebo controlled, parallel group design study.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for sklice

Condition Name

Condition Name for sklice
Intervention Trials
Head Lice 2
SARS-CoV 2 1
Anatomic Stage IV Breast Cancer AJCC v8 1
COVID-19 1
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Condition MeSH

Condition MeSH for sklice
Intervention Trials
Lice Infestations 3
COVID-19 1
Triple Negative Breast Neoplasms 1
Breast Neoplasms 1
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Clinical Trial Locations for sklice

Trials by Country

Trials by Country for sklice
Location Trials
United States 8
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Trials by US State

Trials by US State for sklice
Location Trials
California 2
Florida 2
Maryland 1
Washington 1
Tennessee 1
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Clinical Trial Progress for sklice

Clinical Trial Phase

Clinical Trial Phase for sklice
Clinical Trial Phase Trials
Phase 3 2
Phase 2 2
Phase 1 1
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Clinical Trial Status

Clinical Trial Status for sklice
Clinical Trial Phase Trials
Completed 3
Withdrawn 1
Not yet recruiting 1
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Clinical Trial Sponsors for sklice

Sponsor Name

Sponsor Name for sklice
Sponsor Trials
bioRASI, LLC 2
Taro Pharmaceuticals USA 1
Teva Pharmaceuticals USA 1
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Sponsor Type

Sponsor Type for sklice
Sponsor Trials
Industry 6
Other 2
NIH 1
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