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. 2014:8:149-56.
doi: 10.2147/OPTH.S55456. Epub 2013 Dec 28.

Phase III safety and efficacy study of long-term brinzolamide/timolol fixed combination in Japanese patients with open-angle glaucoma or ocular hypertension

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Phase III safety and efficacy study of long-term brinzolamide/timolol fixed combination in Japanese patients with open-angle glaucoma or ocular hypertension

Masayuki Nakajima et al. Clin Ophthalmol. 2014.

Abstract

Background: The purpose of this study was to evaluate the safety and efficacy of a long-term, twice-daily brinzolamide 1%/timolol 0.5% fixed combination ophthalmic suspension (BRINZ/TIM-FC) in Japanese patients with open-angle glaucoma (primary open-angle, normal-tension, exfoliation, or pigmentary) or ocular hypertension.

Methods: This was a prospective, nonrandomized, multicenter, open-label, Phase III study of Japanese patients aged ≥20 years with diagnoses of open-angle glaucoma or ocular hypertension. Patients were treated with topical BRINZ/TIM-FC twice daily for 52 weeks. The primary endpoint was mean reduction from baseline in intraocular pressure. Data were analyzed using repeated-measures analysis of variance and t-tests. Adverse events and ophthalmic, physiologic, and laboratory parameters were measured throughout the study as safety endpoints. A total of 126 patients (mean ± SD age, 63±12 years) were enrolled, and 125 received BRINZ/TIM-FC.

Results: Mean intraocular pressure was significantly reduced from baseline at weeks 4 through 52, with changes ranging from -4.1 mmHg to -5.7 mmHg (P<0.0001, all time points). Adverse events related to BRINZ/TIM-FC treatment were observed in 22% of patients. No substantial changes from baseline were observed in ophthalmic, physiologic, or laboratory variables.

Conclusion: Long-term, twice-daily BRINZ/TIM-FC therapy produced and maintained significant intraocular pressure reductions and was generally well tolerated in Japanese patients with open-angle glaucoma or ocular hypertension.

Keywords: Japan; clinical trial; intraocular pressure; long-term safety.

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Figures

Figure 1
Figure 1
Mean IOP reduction from baseline at 9 am (preinstillation) and 11 am (2 hours post instillation) with BRINZ/TIM-FC. Data points represent the mean ± standard deviation; n=125 at baseline and 11 am time points; n=118 at week 26 and week 52 9 am time points. Abbreviations: BRINZ/TIM-FC, brinzolamide 1%/timolol 0.5% fixed combination; IOP, intraocular pressure; W, week.
Figure 2
Figure 2
Mean IOP over time from baseline to week 52 with BRINZ/TIM-FC. Data points represent mean ± standard deviation; n=125 at baseline and 11 am time points; n=118 at week 26 and week 52 9 am time points. Abbreviations: BRINZ/TIM-FC, brinzolamide 1%/timolol 0.5% fixed combination; IOP, intraocular pressure; W, week.

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