首页> 外文期刊>European journal of ophthalmology >Latanoprost 0.005% test formulation is as effective as Xalatan? in patients with ocular hypertension and primary open-angle glaucoma.
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Latanoprost 0.005% test formulation is as effective as Xalatan? in patients with ocular hypertension and primary open-angle glaucoma.

机译:拉坦前列素0.005%测试制剂与Xalatan一样有效吗?高眼压和原发性开角型青光眼的患者。

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摘要

To determine if a test formulation of latanoprost 0.005% (Bausch & Lomb) eyedrops reduced intraocular pressure (IOP) as well as Xalatan? (latanoprost 0.005%) in patients with ocular hypertension (OH) or primary open-angle glaucoma (POAG).This multicenter, randomized, investigator-masked, parallel-group study allocated 266 patients with OH or POAG in a 1:1 ratio to latanoprost or Xalatan administered once daily for 6 weeks. The primary endpoint was the mean change in 8:00 AM IOP of the study eye from baseline to week 6. Secondary endpoints included mean change in 8:00 AM IOP from baseline to week 2, and in 12:00 noon and 4:00 PM IOP from baseline to week 2 and week 6. The safety and tolerability of both drugs were also assessed.Both study groups had comparable demographics and baseline characteristics. The mean (SD) change in 8:00 AM IOP from baseline to week 6 was -7.29 (2.61) and -7.54 (2.80) mmHg with latanoprost and Xalatan, respectively. Latanoprost was found noninferior to Xalatan in the primary analysis (mean [SEM] treatment difference, 0.252 [0.504] mmHg; 95% confidence interval [CI] -0.408, 0.913; p = 0.0001; noninferiority margin, 1.5 mmHg) and met the predefined definition of equivalence to Xalatan (95% CI within [-1.5, 1.5 mmHg] margin). The IOP-lowering effects of latanoprost and Xalatan were comparable at all assessed time points. Both study treatments demonstrated a comparable safety and tolerability profile.Bausch & Lomb latanoprost 0.005% is clinically equivalent to Xalatan for treating OH and POAG as demonstrated through this unique comparative trial.
机译:为了确定0.005%拉坦前列素(Bausch&Lomb)眼药水的测试制剂是否降低了眼内压(IOP)以及Xalatan? (Latanprost 0.005%)用于高眼压(OH)或原发性开角型青光眼(POAG)患者。这项多中心,随机,研究者掩盖的平行分组研究以1:1的比例分配了266例OH或POAG患者拉坦前列素或Xalatan每天给药一次,持续6周。主要终点是研究眼睛从基线到第6周的8:00 AM IOP的平均变化。次要终点包括从基线到第2周的8:00 AM IOP的平均变化,以及中午12:00和4:00。从基线到第2周和第6周的PM IOP也进行了评估。两种药物的安全性和耐受性也进行了评估。两个研究组的人口统计学和基线特征均相当。从基线到第6周上午8:00眼压的平均(SD)变化为拉坦前列素和Xalatan,分别为-7.29(2.61)和-7.54(2.80)mmHg。在初步分析中发现拉坦前列素不次于Xalatan(平均[SEM]治疗差异,0.252 [0.504] mmHg; 95%置信区间[CI] -0.408,0.913; p = 0.0001;非劣效性边界,1.5 mmHg)且符合预定标准定义与Xalatan等效(95%CI在[-1.5,1.5 mmHg]范围内)。在所有评估的时间点,拉坦前列素和Xalatan降低IOP的效果均相当。两种研究方法均显示出可比较的安全性和耐受性。通过这一独特的对比试验证明,Bausch&Lomb latanoprost 0.005%在临床上等同于Xalatan用于治疗OH和POAG。

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