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Novel ocular antihypertensive compounds in clinical trials

INTRODUCTION: Glaucoma is a multifactorial disease characterized by progressive optic nerve injury and visual field defects. Elevated intraocular pressure (IOP) is the most widely recognized risk factor for the onset and progression of open-angle glaucoma, and IOP-lowering medications comprise the p...

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Autores principales: Chen, June, Runyan, Stephen A, Robinson, Michael R
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3104796/
https://www.ncbi.nlm.nih.gov/pubmed/21629573
http://dx.doi.org/10.2147/OPTH.S15971
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author Chen, June
Runyan, Stephen A
Robinson, Michael R
author_facet Chen, June
Runyan, Stephen A
Robinson, Michael R
author_sort Chen, June
collection PubMed
description INTRODUCTION: Glaucoma is a multifactorial disease characterized by progressive optic nerve injury and visual field defects. Elevated intraocular pressure (IOP) is the most widely recognized risk factor for the onset and progression of open-angle glaucoma, and IOP-lowering medications comprise the primary treatment strategy. IOP elevation in glaucoma is associated with diminished or obstructed aqueous humor outflow. Pharmacotherapy reduces IOP by suppressing aqueous inflow and/or increasing aqueous outflow. PURPOSE: This review focuses on novel non-FDA approved ocular antihypertensive compounds being investigated for IOP reduction in ocular hypertensive and glaucoma patients in active clinical trials within approximately the past 2 years. METHODS: The mode of IOP reduction, pharmacology, efficacy, and safety of these new agents were assessed. Relevant drug efficacy and safety trials were identified from searches of various scientific literature databases and clinical trial registries. Compounds with no specified drug class, insufficient background information, reformulations, and fixed-combinations of marketed drugs were not considered. RESULTS: The investigational agents identified comprise those that act on the same targets of established drug classes approved by the FDA (ie, prostaglandin analogs and β-adrenergic blockers) as well as agents belonging to novel drug classes with unique mechanisms of action. Novel targets and compounds evaluated in clinical trials include an actin polymerization inhibitor (ie, latrunculin), Rho-associated protein kinase inhibitors, adenosine receptor analogs, an angiotensin II type 1 receptor antagonist, cannabinoid receptor agonists, and a serotonin receptor antagonist. CONCLUSION: The clinical value of novel compounds for the treatment of glaucoma will depend ultimately on demonstrating favorable efficacy and benefit-to-risk ratios relative to currently approved prostaglandin analogs and β-blockers and/or having complementary modes of action.
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spelling pubmed-31047962011-05-31 Novel ocular antihypertensive compounds in clinical trials Chen, June Runyan, Stephen A Robinson, Michael R Clin Ophthalmol Review INTRODUCTION: Glaucoma is a multifactorial disease characterized by progressive optic nerve injury and visual field defects. Elevated intraocular pressure (IOP) is the most widely recognized risk factor for the onset and progression of open-angle glaucoma, and IOP-lowering medications comprise the primary treatment strategy. IOP elevation in glaucoma is associated with diminished or obstructed aqueous humor outflow. Pharmacotherapy reduces IOP by suppressing aqueous inflow and/or increasing aqueous outflow. PURPOSE: This review focuses on novel non-FDA approved ocular antihypertensive compounds being investigated for IOP reduction in ocular hypertensive and glaucoma patients in active clinical trials within approximately the past 2 years. METHODS: The mode of IOP reduction, pharmacology, efficacy, and safety of these new agents were assessed. Relevant drug efficacy and safety trials were identified from searches of various scientific literature databases and clinical trial registries. Compounds with no specified drug class, insufficient background information, reformulations, and fixed-combinations of marketed drugs were not considered. RESULTS: The investigational agents identified comprise those that act on the same targets of established drug classes approved by the FDA (ie, prostaglandin analogs and β-adrenergic blockers) as well as agents belonging to novel drug classes with unique mechanisms of action. Novel targets and compounds evaluated in clinical trials include an actin polymerization inhibitor (ie, latrunculin), Rho-associated protein kinase inhibitors, adenosine receptor analogs, an angiotensin II type 1 receptor antagonist, cannabinoid receptor agonists, and a serotonin receptor antagonist. CONCLUSION: The clinical value of novel compounds for the treatment of glaucoma will depend ultimately on demonstrating favorable efficacy and benefit-to-risk ratios relative to currently approved prostaglandin analogs and β-blockers and/or having complementary modes of action. Dove Medical Press 2011 2011-05-20 /pmc/articles/PMC3104796/ /pubmed/21629573 http://dx.doi.org/10.2147/OPTH.S15971 Text en © 2011 Chen et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Review
Chen, June
Runyan, Stephen A
Robinson, Michael R
Novel ocular antihypertensive compounds in clinical trials
title Novel ocular antihypertensive compounds in clinical trials
title_full Novel ocular antihypertensive compounds in clinical trials
title_fullStr Novel ocular antihypertensive compounds in clinical trials
title_full_unstemmed Novel ocular antihypertensive compounds in clinical trials
title_short Novel ocular antihypertensive compounds in clinical trials
title_sort novel ocular antihypertensive compounds in clinical trials
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3104796/
https://www.ncbi.nlm.nih.gov/pubmed/21629573
http://dx.doi.org/10.2147/OPTH.S15971
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