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Bimatoprost Implant: First Approval

Bimatoprost implant (Durysta™), developed by Allergan, is a sustained-release drug delivery system containing bimatoprost, a prostaglandin analogue with ocular hypotensive activity. The implant, administered intracamerally, involves the use of a biodegradable, solid polymer drug delivery system for...

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Detalles Bibliográficos
Autor principal: Shirley, Matt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7303088/
https://www.ncbi.nlm.nih.gov/pubmed/32447639
http://dx.doi.org/10.1007/s40266-020-00769-8
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author Shirley, Matt
author_facet Shirley, Matt
author_sort Shirley, Matt
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description Bimatoprost implant (Durysta™), developed by Allergan, is a sustained-release drug delivery system containing bimatoprost, a prostaglandin analogue with ocular hypotensive activity. The implant, administered intracamerally, involves the use of a biodegradable, solid polymer drug delivery system for slow, sustained drug release, designed to lower intraocular pressure (IOP) over a 4- to 6-months period. In March 2020, bimatoprost implant received its first approval, in the USA, for use to reduce IOP in patients with open angle glaucoma (OAG) or ocular hypertension (OHT). Allergan’s clinical development programme for bimatoprost implant is ongoing. This article summarizes the milestones in the development of bimatoprost implant leading to this first approval for use in the reduction of IOP in patients with OAG or OHT.
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spelling pubmed-73030882020-06-22 Bimatoprost Implant: First Approval Shirley, Matt Drugs Aging AdisInsight Report Bimatoprost implant (Durysta™), developed by Allergan, is a sustained-release drug delivery system containing bimatoprost, a prostaglandin analogue with ocular hypotensive activity. The implant, administered intracamerally, involves the use of a biodegradable, solid polymer drug delivery system for slow, sustained drug release, designed to lower intraocular pressure (IOP) over a 4- to 6-months period. In March 2020, bimatoprost implant received its first approval, in the USA, for use to reduce IOP in patients with open angle glaucoma (OAG) or ocular hypertension (OHT). Allergan’s clinical development programme for bimatoprost implant is ongoing. This article summarizes the milestones in the development of bimatoprost implant leading to this first approval for use in the reduction of IOP in patients with OAG or OHT. Springer International Publishing 2020-05-23 2020 /pmc/articles/PMC7303088/ /pubmed/32447639 http://dx.doi.org/10.1007/s40266-020-00769-8 Text en © The Author(s) 2020, corrected publication 2020 Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle AdisInsight Report
Shirley, Matt
Bimatoprost Implant: First Approval
title Bimatoprost Implant: First Approval
title_full Bimatoprost Implant: First Approval
title_fullStr Bimatoprost Implant: First Approval
title_full_unstemmed Bimatoprost Implant: First Approval
title_short Bimatoprost Implant: First Approval
title_sort bimatoprost implant: first approval
topic AdisInsight Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7303088/
https://www.ncbi.nlm.nih.gov/pubmed/32447639
http://dx.doi.org/10.1007/s40266-020-00769-8
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