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Last Updated: March 28, 2024

CLINICAL TRIALS PROFILE FOR XIIDRA


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All Clinical Trials for Xiidra

Trial ID Title Status Sponsor Phase Start Date Summary
NCT03408015 ↗ Effects of Xiidra on Closed Eye Tear Film Leukocytes in Dry Eye Disease Withdrawn Shire Phase 4 2019-01-01 Every night during sleep, there is an accumulation of white blood cells in the closed eye. The closed eye white blood cells are predominantly neutrophils, but there is a small population (3%) of T cells. The effects of these closed eye white blood cells on dry eye disease pathogenesis have yet to be fully elucidated, but preliminary evidence suggests that closed eye neutrophils may have an associated hyperactivity and increased degranulation in dry eye disease that could contribute to epithelial instability. As an anti-T cell therapy, Xiidra offers an opportunity to better understand how the closed eye white blood cells are recruited and activated. This study also seeks to verify the proposed mechanism of action.
NCT03408015 ↗ Effects of Xiidra on Closed Eye Tear Film Leukocytes in Dry Eye Disease Withdrawn University of Alabama at Birmingham Phase 4 2019-01-01 Every night during sleep, there is an accumulation of white blood cells in the closed eye. The closed eye white blood cells are predominantly neutrophils, but there is a small population (3%) of T cells. The effects of these closed eye white blood cells on dry eye disease pathogenesis have yet to be fully elucidated, but preliminary evidence suggests that closed eye neutrophils may have an associated hyperactivity and increased degranulation in dry eye disease that could contribute to epithelial instability. As an anti-T cell therapy, Xiidra offers an opportunity to better understand how the closed eye white blood cells are recruited and activated. This study also seeks to verify the proposed mechanism of action.
NCT03431272 ↗ Use of 5.0% Lifitegrast Ophthalmic Solution for the Treatment of Dry Eye Disease in Contact Lens Wearers Withdrawn Shire Phase 4 2018-11-01 Discomfort with contact lens wear is the biggest reason why people stop wearing contact lenses. The investigators believe that inflammation is one of the causes of discomfort, and by blocking the inflammation using lifitegrast, the investigators may be able to relieve some of that discomfort. This study will enroll 50 subjects with contact lens discomfort and will receive lifitegrast to use over a period of approximately 3 months.
NCT03431272 ↗ Use of 5.0% Lifitegrast Ophthalmic Solution for the Treatment of Dry Eye Disease in Contact Lens Wearers Withdrawn University of Alabama at Birmingham Phase 4 2018-11-01 Discomfort with contact lens wear is the biggest reason why people stop wearing contact lenses. The investigators believe that inflammation is one of the causes of discomfort, and by blocking the inflammation using lifitegrast, the investigators may be able to relieve some of that discomfort. This study will enroll 50 subjects with contact lens discomfort and will receive lifitegrast to use over a period of approximately 3 months.
NCT03952481 ↗ Effect of Lifitegrast 5% on Tear Film Markers Withdrawn Novartis Phase 4 2021-03-01 The purpose of this study is to assess the duration of time (in weeks) for improvement in objective dry eye markers for people who are placed on lifitegrast 0.5% (Xiidra®), an FDA-approved therapy for dry eyes.
NCT03952481 ↗ Effect of Lifitegrast 5% on Tear Film Markers Withdrawn Shire Human Genetic Therapies, Inc. Phase 4 2021-03-01 The purpose of this study is to assess the duration of time (in weeks) for improvement in objective dry eye markers for people who are placed on lifitegrast 0.5% (Xiidra®), an FDA-approved therapy for dry eyes.
NCT03952481 ↗ Effect of Lifitegrast 5% on Tear Film Markers Withdrawn Weill Medical College of Cornell University Phase 4 2021-03-01 The purpose of this study is to assess the duration of time (in weeks) for improvement in objective dry eye markers for people who are placed on lifitegrast 0.5% (Xiidra®), an FDA-approved therapy for dry eyes.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Xiidra

Condition Name

Condition Name for Xiidra
Intervention Trials
Dry Eye 7
Dry Eye Syndromes 3
Keratoconjunctivitis Sicca 1
Ocular Discomfort 1
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Condition MeSH

Condition MeSH for Xiidra
Intervention Trials
Dry Eye Syndromes 12
Keratoconjunctivitis Sicca 10
Eye Diseases 6
Inflammation 2
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Clinical Trial Locations for Xiidra

Trials by Country

Trials by Country for Xiidra
Location Trials
United States 25
Canada 2
United Arab Emirates 1
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Trials by US State

Trials by US State for Xiidra
Location Trials
New York 3
Tennessee 2
Pennsylvania 2
Alabama 2
Missouri 2
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Clinical Trial Progress for Xiidra

Clinical Trial Phase

Clinical Trial Phase for Xiidra
Clinical Trial Phase Trials
Phase 4 10
Phase 2 2
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Clinical Trial Status

Clinical Trial Status for Xiidra
Clinical Trial Phase Trials
Recruiting 6
Withdrawn 3
Active, not recruiting 1
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Clinical Trial Sponsors for Xiidra

Sponsor Name

Sponsor Name for Xiidra
Sponsor Trials
Shire 2
University of Alabama at Birmingham 2
Novartis 2
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Sponsor Type

Sponsor Type for Xiidra
Sponsor Trials
Industry 10
Other 10
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