2004TherapyRequires access

An update on bimatoprost (Lumigan®) in glaucoma therapy

Robert J. Noecker, Melissa Earl

Open publisher page 2 citations

Abstract

The prostamide bimatoprost (Lumigan®, Allergan Inc.) has been proven highly effective as monotherapy, adjunctive, and replacement therapy for lowering intraocular pressure (IOP) and providing good diurnal control of IOP in patients with open-angle glaucoma and ocular hypertension. Target pressure results from large, randomized, multicenter clinical trials comparing bimatoprost with timolol, latanoprost (Xalatan®, Pharmacia & Upjohn), travoprost (Travatan®, Alcon laboratories), fixed combination timolol/dorzolamide (Cosopt®, Merck Inc.) or latanoprost and timolol gel have been analyzed. In each of the analyses, patients were more likely to achieve low target pressures with bimatoprost than with the other medications. Patients on bimatoprost therapy achieve low IOP levels that are maintained throughout the day and night, and long-term trials have shown that the efficacy of bimatoprost is sustained. Bimatoprost has been proven to be safe and well tolerated in postmarketing surveillance and, as a once-daily d...

About this research paper

What this paper is about

The prostamide bimatoprost (Lumigan®, Allergan Inc.) has been proven highly effective as monotherapy, adjunctive, and replacement therapy for lowering intraocular pressure (IOP) and providing good diurnal control of IOP in patients with open-angle glaucoma and ocular hypertension. Target pressure results from large, randomized, multicenter clinical trials comparing bimatoprost with timolol, latanoprost (Xalatan®, Pharmacia & Upjohn), travoprost (Travatan®, Alcon laboratories), fixed combination timolol/dorzolamide (Cosopt®, Merck Inc.) or latanoprost and timolol gel have been analyzed. In each of the analyses, patients were more likely to achieve low target pressures with bimatoprost than with the other medications. Patients on bimatoprost therapy achieve low IOP levels that are maintained throughout the day and night, and long-term trials have shown that the efficacy of bimatoprost is sustained. Bimatoprost has been proven to be safe and well tolerated in postmarketing surveillance and, as a once-daily d...

Why it matters

OpenAlex reports 2 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

The prostamide bimatoprost (Lumigan®, Allergan Inc.) has been proven highly effective as monotherapy, adjunctive, and replacement therapy for lowering intraocular pressure (IOP) and providing good diurnal control of IOP in patients with open-angle glaucoma and ocular hypertension. Target pressure results from large, randomized, multicenter clinical trials comparing bimatoprost with timolol, latanoprost (Xalatan®, Pharmacia & Upjohn), travoprost (Travatan®, Alcon laboratories), fixed combination timolol/dorzolamide (Cosopt®, Merck Inc.) or latanoprost and timolol gel have been analyzed. In each of the analyses, patients were more likely to achieve low target pressures with bimatoprost than with the other medications. Patients on bimatoprost therapy achieve low IOP levels that are maintained throughout the day and night, and long-term trials have shown that the efficacy of bimatoprost is sustained. Bimatoprost has been proven to be safe and well tolerated in postmarketing surveillance and, as a once-daily d...

Key concepts: Bimatoprost, Latanoprost, Travoprost, Dorzolamide, Medicine, Timolol, Ophthalmology, Intraocular pressure

Related papers

Back to paper searchBrowse research topicsOriginal source
An update on bimatoprost (Lumigan®) in glaucoma therapy — Research Paper | ScholarLens