Intraocular Pressure-lowering Efficacy of Brinzolamide When Added to Travoprost/Timolol Fixed Combination as Adjunctive Therapy

被引:13
|
作者
Goldberg, Ivan [2 ]
Crowston, Jonathan G. [3 ]
Jasek, Mark C. [4 ]
Stewart, Jeanette A. [1 ]
Stewart, William C. [1 ]
机构
[1] PRN Pharmaceut Res Network LLC, Charleston, SC 29406 USA
[2] Sydney Eye Hosp, Glaucoma Serv, Sydney, NSW, Australia
[3] Univ Melbourne, Ctr Eye Res Australia Fdn, Melbourne, Vic, Australia
[4] Alcon Labs Inc, Ft Worth, TX 76101 USA
关键词
brinzolamide; travoprost/timolol fixed combination; intraocular pressure; adjunctive therapy; ocular hypertension; primary open-angle glaucoma; OPEN-ANGLE GLAUCOMA; OCULAR HYPERTENSION; TOPICAL BRINZOLAMIDE; TIMOLOL MALEATE; UNITED-STATES; LATANOPROST; SAFETY; DORZOLAMIDE; 1-PERCENT; 0.004-PERCENT;
D O I
10.1097/IJG.0b013e3181fc8142
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: To compare the efficacy of brinzolamide versus placebo when added to travoprost/timolol fixed combination (TTFC) in uncontrolled patients. Patients and Methods: This was a prospective, double-masked, randomized, placebo-controlled, parallel comparison of ocular hypertensive or primary open-angle glaucoma patients. Patients treated with a prostaglandin-based mono or adjunctive therapy were changed to TTFC qam (every day dosing) for 4 weeks. Patients with an intraocular pressure (IOP) of 19 to 32 mm Hg at 08:00 hours underwent additional measurements at 12:00 and 16:00 hours. Patients were then randomized to either placebo or brinzolamide given twice daily in addition to TTFC. At week 12, patients had their IOP measurements repeated. Results: The per protocol dataset consisting of 78 placebo and 75 brinzolamide-treated patients decreased mean diurnal IOP (mm Hg) as well as IOP at all 3 individual time points (P <= 0.005). Brinzolamide reduced the mean diurnal IOP from 20.3 +/- 2.0 to 17.5 +/- 2.6, whereas placebo reduced IOP from 20.9 +/- 2.7 to 19.4 +/- 3.8. The mean diurnal IOP was reduced from baseline and for the 08:00 and 16:00 hours time points in the brinzolamide group compared with placebo (P <= 0.014). There were 30 adverse events with placebo and 24 with brinzolamide (intent-to-treat). There was no statistical difference for the side-effect profile observed between the treatment groups (P = 0.47). Conclusions: This study suggests that brinzolamide may be safely added to TTFC therapy to provide further significant reduction in IOP patients with ocular hypertensive or primary open-angle glaucoma.
引用
收藏
页码:55 / 59
页数:5
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