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Last Updated: October 17, 2019

DrugPatentWatch Database Preview

CLINICAL TRIALS PROFILE FOR TAFLUPROST

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Clinical Trials for Tafluprost

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00596791 Ocular Signs and Symptoms in Glaucoma Patients Switched From Latanoprost 0.005% to Preservative Free Tafluprost Eye Drops Completed Santen Oy Phase 3 2008-01-01 The purpose of this study is to investigate if changes in ocular signs and symptoms occur in patients with ocular hypertension or glaucoma when they switch from latanoprost 0.005% (Xalatan) to preservative free Tafluprost eye drops.
NCT00918346 Pharmacodynamics of Tafluprost 0.0015% Eye Drops: a Comparison Between the Preserved and Unpreserved Formulation Completed Santen Oy Phase 3 2005-09-01 The objective of this study is to investigate the pharmacodynamics (as expressed in intraocular pressure [IOP]) of two formulations of tafluprost 0.0015% eyedrops (preserved and unpreserved) in patients with open-angle glaucoma or ocular hypertension. The primary aim of this study is to show that IOP reduction between the two formulations is equivalent at the end of the 4 week treatment period.
NCT00966940 Efficacy and Safety of Travoprost 0.004% Versus Tafluprost 0.0015% in Patients With Primary Open-angle Glaucoma or Ocular Hypertension Completed Alcon Research Phase 4 2009-09-01 The purpose of this study is to assess the safety and efficacy of Travoprost 0.004% and Tafluprost 0.0015% in patients with primary open angle glaucoma or ocular hypertension when both medications are administered in the evening.
NCT01026831 Preservative-Free MK2452 (Tafluprost) for Open-Angle Glaucoma/Ocular Hypertension (MK2452-001)(COMPLETED) Completed Merck Sharp & Dohme Corp. Phase 3 2010-01-01 This study was to compare the safety and efficacy of the preservative-free formulation of 0.0015% MK2452 (tafluprost) and preservative-free 0.5% timolol maleate in patients with open-angle glaucoma and ocular hypertension. This study was to demonstrate that the preservative-free formulation of 0.0015% tafluprost is non-inferior to preservative-free 0.5% timolol maleate.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Tafluprost

Condition Name

Condition Name for Tafluprost
Intervention Trials
Ocular Hypertension 16
Glaucoma 8
Open-Angle Glaucoma 7
Primary Open Angle Glaucoma 2
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Condition MeSH

Condition MeSH for Tafluprost
Intervention Trials
Glaucoma 22
Ocular Hypertension 18
Glaucoma, Open-Angle 15
Hypertension 14
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Clinical Trial Locations for Tafluprost

Trials by Country

Trials by Country for Tafluprost
Location Trials
United States 8
Finland 5
Italy 3
Austria 3
Greece 2
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Trials by US State

Trials by US State for Tafluprost
Location Trials
California 2
New York 1
Georgia 1
Florida 1
Pennsylvania 1
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Clinical Trial Progress for Tafluprost

Clinical Trial Phase

Clinical Trial Phase for Tafluprost
Clinical Trial Phase Trials
Phase 4 10
Phase 3 10
Phase 1/Phase 2 1
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Clinical Trial Status

Clinical Trial Status for Tafluprost
Clinical Trial Phase Trials
Completed 18
Recruiting 3
Unknown status 2
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Clinical Trial Sponsors for Tafluprost

Sponsor Name

Sponsor Name for Tafluprost
Sponsor Trials
Santen Oy 8
Aristotle University Of Thessaloniki 3
Santen Pharmaceutical Co., Ltd. 2
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Sponsor Type

Sponsor Type for Tafluprost
Sponsor Trials
Industry 17
Other 12
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Serving leading biopharmaceutical companies globally:

Moodys
Colorcon
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AstraZeneca
Medtronic

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