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Last Updated: August 8, 2020

DrugPatentWatch Database Preview

CLINICAL TRIALS PROFILE FOR LOTEPREDNOL ETABONATE

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All Clinical Trials for Loteprednol Etabonate

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00366691 Comparison of Acular LS With Lotemax to Prevent Inflammation After Cataract Surgery and Intraocular Lens Implantation Completed Medical University of South Carolina Phase 4 2006-02-01 The purpose of this study is to compare the effectiveness of Acular LS® and Lotemax® in the prevention of inflammation in the eye after cataract surgery. Acular LS is made by Allergan, Inc. It is a nonsteroidal anti-inflammatory drug (NSAID) and is approved by the Food and Drug Administration (FDA) for use following cataract surgery. Lotemax is made by Bausch & Lomb. It is a steroid and is also approved by the FDA for use following cataract surgery.
NCT00420628 Pediatric Zylet Safety and Efficacy Study Completed Bausch & Lomb Incorporated Phase 4 2006-11-01 A multicenter study to evaluate the safety and efficacy of Zylet compared to vehicle in children aged 0-6 for the management of lid inflammation (chalazion/hordeolum)
NCT00447577 Zylet vs TobraDex in Blepharokeratoconjunctivitis Completed Bausch & Lomb Incorporated Phase 4 2007-01-01 The objective of this study is to evaluate the safety and efficacy of Zylet vs. Tobradex in the treatment of ocular inflammation associated with blepharokeratoconjunctivitis
NCT00560638 Loteprednol Etabonate Opthalmic Suspension for the Treatment of Dry Eye Completed Bausch & Lomb Incorporated Phase 2 2005-11-01 This was a single-center, randomized, double-masked, placebo-controlled, parallel-group, 4-visit, CAE (Controlled Adverse Environment) study lasting approximately 4 weeks. Subjects were randomized to receive loteprednol etabonate ophthalmic suspension, 0.5% or placebo (vehicle of loteprednol etabonate ophthalmic suspension, 0.5%) and instructed to dose bilaterally either TID or QID according to randomization.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Loteprednol Etabonate

Condition Name

Condition Name for Loteprednol Etabonate
Intervention Trials
Inflammation 5
Pain 4
Cataract 4
Keratoconjunctivitis Sicca 3
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Condition MeSH

Condition MeSH for Loteprednol Etabonate
Intervention Trials
Inflammation 13
Cataract 9
Conjunctivitis 8
Keratoconjunctivitis Sicca 7
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Clinical Trial Locations for Loteprednol Etabonate

Trials by Country

Trials by Country for Loteprednol Etabonate
Location Trials
United States 123
Singapore 2
Korea, Republic of 2
Israel 1
Brazil 1
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Trials by US State

Trials by US State for Loteprednol Etabonate
Location Trials
California 11
New York 11
Missouri 7
Massachusetts 7
Ohio 6
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Clinical Trial Progress for Loteprednol Etabonate

Clinical Trial Phase

Clinical Trial Phase for Loteprednol Etabonate
Clinical Trial Phase Trials
Phase 4 14
Phase 3 14
Phase 2 4
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Clinical Trial Status

Clinical Trial Status for Loteprednol Etabonate
Clinical Trial Phase Trials
Completed 30
Recruiting 6
Unknown status 4
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Clinical Trial Sponsors for Loteprednol Etabonate

Sponsor Name

Sponsor Name for Loteprednol Etabonate
Sponsor Trials
Bausch & Lomb Incorporated 20
Kala Pharmaceuticals, Inc. 7
Zhongshan Ophthalmic Center, Sun Yat-sen University 1
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Sponsor Type

Sponsor Type for Loteprednol Etabonate
Sponsor Trials
Industry 31
Other 17
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