Latanoprostene bunod ophthalmic solution 0.024% in the treatment of open-angle glaucoma: design, development, and place in therapy

Victoria M Addis, Eydie Miller-Ellis Division of Glaucoma, Scheie Eye Institute, University of Pennsylvania, Philadelphia, PA, USAAbstract: Latanoprostene bunod (LBN) 0.024%, a modified prostaglandin analog, was approved on November 2, 2017, for the reduction of IOP in patients with open-angle glauc...

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Autores principales: Addis VM, Miller-Ellis E
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Lenguaje:EN
Publicado: Dove Medical Press 2018
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Acceso en línea:https://doaj.org/article/c9383bc0ee124c8e94cd9995197c5860
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spelling oai:doaj.org-article:c9383bc0ee124c8e94cd9995197c58602021-12-02T02:47:49ZLatanoprostene bunod ophthalmic solution 0.024% in the treatment of open-angle glaucoma: design, development, and place in therapy1177-5483https://doaj.org/article/c9383bc0ee124c8e94cd9995197c58602018-12-01T00:00:00Zhttps://www.dovepress.com/latanoprostene-bunod-ophthalmic-solution-0024-in-the-treatment-of-open-peer-reviewed-article-OPTHhttps://doaj.org/toc/1177-5483Victoria M Addis, Eydie Miller-Ellis Division of Glaucoma, Scheie Eye Institute, University of Pennsylvania, Philadelphia, PA, USAAbstract: Latanoprostene bunod (LBN) 0.024%, a modified prostaglandin analog, was approved on November 2, 2017, for the reduction of IOP in patients with open-angle glaucoma (OAG) or ocular hypertension (OHT). LBN works by combining the IOP-lowering effects of the prostaglandin analogs (through the uveoscleral pathway) with nitric oxide-induced relaxation of the trabecular meshwork and Schlemm’s canal. Nitric oxide-induced relaxation of the trabecular meshwork and Schlemm’s canal leads to increased outflow through the trabecular meshwork and thus lowering of IOP. LBN has now been shown in multiple clinical studies to be effective and safe. In this article, we summarize the clinical trials that led to LBN’s approval as well as the comparative studies that have been done to evaluate the efficacy of this drug as compared to other US Food and Drug Administration (FDA)-approved therapies for OAG and OHT. We then review the side effects of treatment that were seen in each of these studies. Finally, we will attempt to discuss the place of this drug in therapy for patients with OAG. Keywords: latanoprostene bunod, open-angle glaucoma, ocular hypertension, modified prostaglandin analog, nitric oxide, treatment-associated adverse eventAddis VMMiller-Ellis EDove Medical PressarticleLatanoprostene bunodopen angle glaucomaocular hypertensionmodified prostaglandin analognitric oxidetreatment-associated adverse eventOphthalmologyRE1-994ENClinical Ophthalmology, Vol Volume 12, Pp 2649-2657 (2018)
institution DOAJ
collection DOAJ
language EN
topic Latanoprostene bunod
open angle glaucoma
ocular hypertension
modified prostaglandin analog
nitric oxide
treatment-associated adverse event
Ophthalmology
RE1-994
spellingShingle Latanoprostene bunod
open angle glaucoma
ocular hypertension
modified prostaglandin analog
nitric oxide
treatment-associated adverse event
Ophthalmology
RE1-994
Addis VM
Miller-Ellis E
Latanoprostene bunod ophthalmic solution 0.024% in the treatment of open-angle glaucoma: design, development, and place in therapy
description Victoria M Addis, Eydie Miller-Ellis Division of Glaucoma, Scheie Eye Institute, University of Pennsylvania, Philadelphia, PA, USAAbstract: Latanoprostene bunod (LBN) 0.024%, a modified prostaglandin analog, was approved on November 2, 2017, for the reduction of IOP in patients with open-angle glaucoma (OAG) or ocular hypertension (OHT). LBN works by combining the IOP-lowering effects of the prostaglandin analogs (through the uveoscleral pathway) with nitric oxide-induced relaxation of the trabecular meshwork and Schlemm’s canal. Nitric oxide-induced relaxation of the trabecular meshwork and Schlemm’s canal leads to increased outflow through the trabecular meshwork and thus lowering of IOP. LBN has now been shown in multiple clinical studies to be effective and safe. In this article, we summarize the clinical trials that led to LBN’s approval as well as the comparative studies that have been done to evaluate the efficacy of this drug as compared to other US Food and Drug Administration (FDA)-approved therapies for OAG and OHT. We then review the side effects of treatment that were seen in each of these studies. Finally, we will attempt to discuss the place of this drug in therapy for patients with OAG. Keywords: latanoprostene bunod, open-angle glaucoma, ocular hypertension, modified prostaglandin analog, nitric oxide, treatment-associated adverse event
format article
author Addis VM
Miller-Ellis E
author_facet Addis VM
Miller-Ellis E
author_sort Addis VM
title Latanoprostene bunod ophthalmic solution 0.024% in the treatment of open-angle glaucoma: design, development, and place in therapy
title_short Latanoprostene bunod ophthalmic solution 0.024% in the treatment of open-angle glaucoma: design, development, and place in therapy
title_full Latanoprostene bunod ophthalmic solution 0.024% in the treatment of open-angle glaucoma: design, development, and place in therapy
title_fullStr Latanoprostene bunod ophthalmic solution 0.024% in the treatment of open-angle glaucoma: design, development, and place in therapy
title_full_unstemmed Latanoprostene bunod ophthalmic solution 0.024% in the treatment of open-angle glaucoma: design, development, and place in therapy
title_sort latanoprostene bunod ophthalmic solution 0.024% in the treatment of open-angle glaucoma: design, development, and place in therapy
publisher Dove Medical Press
publishDate 2018
url https://doaj.org/article/c9383bc0ee124c8e94cd9995197c5860
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AT millerellise latanoprostenebunodophthalmicsolution0024inthetreatmentofopenangleglaucomadesigndevelopmentandplaceintherapy
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