Literature DB >> 10665517

Dose-response evaluation of the ocular hypotensive effect of brinzolamide ophthalmic suspension (Azopt). Brinzolamide Dose-Response Study Group.

L H Silver1.   

Abstract

Brinzolamide is a novel carbonic anhydrase inhibitor that elicits an ocular hypotensive effect when instilled topically. A multicenter, double-masked, placebo-controlled, parallel trial was conducted to evaluate the optimal intraocular pressure (IOP)-lowering concentration and ocular tolerability of topically administered brinzolamide (0.3%, 1%, 2%, and 3%) in patients with primary, open-angle glaucoma or ocular hypertension. After a washout phase, patients were administered brinzolamide or placebo twice daily for 2 weeks. The IOP was measured on days 8 and 15 at 8:00 A.M., and then 2, 4, 8, and 12 hours after dosing, and these measurements were compared with IOP values obtained at the corresponding times during an off-therapy diurnal baseline. All concentrations of brinzolamide produced significantly greater (P<0.005) mean percent IOP reductions and mean IOP reductions compared with placebo. Mean percent IOP changes (mean IOP changes) from baseline for brinzolamide 0.3%, 1%, 2%, and 3% were -11.3% (-3.0 mm Hg), -16.1% (-4.3 mm Hg), -16.1% (-4.4 mm Hg), and -15.4% (-4.2 mm Hg), respectively, when pooled over visit and visit time. Comparisons between concentrations demonstrated that the mean percent IOP reduction for brinzolamide 1.0% was significantly greater than that for the 0.3% concentration (P<0.03), with no difference in efficacy between the 1%, 2%, and 3% concentrations. The incidence of adverse events was dose-dependent, and those related to therapy were usually mild and resolved without treatment. Blurred vision, ocular discomfort, and abnormal taste were the most frequently reported adverse events. Based on these findings, the optimal IOP-lowering concentration of brinzolamide was 1%. When administered twice daily, brinzolamide 1% was well tolerated by patients with primary open-angle glaucoma or ocular hypertension.

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Year:  2000        PMID: 10665517     DOI: 10.1016/s0039-6257(99)00110-1

Source DB:  PubMed          Journal:  Surv Ophthalmol        ISSN: 0039-6257            Impact factor:   6.048


  8 in total

Review 1.  Topical drug therapy in glaucoma.

Authors:  Hemma Resch; Gerhard Garhofer
Journal:  Wien Med Wochenschr       Date:  2006-09

Review 2.  Topical carbonic anhydrase inhibitors and glaucoma in 2021: where do we stand?

Authors:  Ari Stoner; Alon Harris; Francesco Oddone; Aditya Belamkar; Alice Chandra Verticchio Vercellin; Joshua Shin; Ingrida Januleviciene; Brent Siesky
Journal:  Br J Ophthalmol       Date:  2021-08-25       Impact factor: 5.908

Review 3.  Brinzolamide : a review of its use in the management of primary open-angle glaucoma and ocular hypertension.

Authors:  Risto S Cvetkovic; Caroline M Perry
Journal:  Drugs Aging       Date:  2003       Impact factor: 3.923

4.  Effects of brinzolamide on rabbit ocular blood flow in vivo and ex vivo.

Authors:  Ya-Ru Dong; Shi-Wei Huang; Ji-Zhe Cui; Takeshi Yoshitomi
Journal:  Int J Ophthalmol       Date:  2018-05-18       Impact factor: 1.779

5.  Design, optimisation and evaluation of in situ gelling nanoemulsion formulations of brinzolamide.

Authors:  Hemant Bhalerao; K B Koteshwara; Sajeev Chandran
Journal:  Drug Deliv Transl Res       Date:  2020-04       Impact factor: 4.617

6.  Brinzolamide ophthalmic suspension: a review of its pharmacology and use in the treatment of open angle glaucoma and ocular hypertension.

Authors:  Michele Iester
Journal:  Clin Ophthalmol       Date:  2008-09

7.  Effects of brinzolamide vs timolol as an adjunctive medication to latanoprost on circadian intraocular pressure control in primary open-angle glaucoma Japanese patients.

Authors:  Makoto Ishikawa; Takeshi Yoshitomi
Journal:  Clin Ophthalmol       Date:  2009-09-07

8.  Efficacy and safety of brinzolamide/timolol fixed combination compared with timolol in Japanese patients with open-angle glaucoma or ocular hypertension.

Authors:  Keiji Yoshikawa; Jun Kozaki; Hidetaka Maeda
Journal:  Clin Ophthalmol       Date:  2014-02-10
  8 in total

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