首页> 外文期刊>Journal of glaucoma >Noninferiority of Preservative-free Versus BAK-preserved Latanoprost-timolol Fixed Combination Eye Drops in Patients With Open-angle Glaucoma or Ocular Hypertension
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Noninferiority of Preservative-free Versus BAK-preserved Latanoprost-timolol Fixed Combination Eye Drops in Patients With Open-angle Glaucoma or Ocular Hypertension

机译:无防腐剂的无蛋白与巴氏保存的Latanoprost-timolol固定的组合滴眼液在开口角度青光眼或眼高血压患者中

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Precis: Noninferiority of efficacy was demonstrated for a preservative- free latanoprost-timolol fixed combination compared with a BAK-containing formulation at 84 days after treatment in patients with open-angle glaucoma or ocular hypertension. Purpose: The purpose of this study was to compare the effect on intraocular pressure and safety of preservative-free latanoprosttimolol fixed combination (T2347) to benzalkonium chloride-preserved latanoprost-timolol fixed combination in patients with open-angle glaucoma or ocular hypertension. Methods: Phase III, randomized, parallel-group, investigatormasked study in 10 countries. A total of 242 patients aged 18 years or older with open-angle glaucoma or ocular hypertension in both eyes controlled with a preserved latanoprost-timolol fixed combination (15.7 +/- 2.4 mm Hg overall before inclusion) were randomized at day 0 with no washout period to receive the preservativefree alternative T2347 (N = 127) or remain on the preserved comparator (N= 115) for 84 days. Intraocular pressure changes from day 0 were measured at 9: 00 am (+/- 1 hour) on day 42 and day 84, and noninferiority of T2347 to the preserved comparator was analyzed statistically at day 84. Safety parameters were also reported. Results: The mean change in intraocular pressure from baseline to day 84 was -0.49 +/- 1.80mmHg for preservative-free T2347 and -0.49 +/- 2.25mmHg for the preserved comparator. These results met the noninferiority limits. Similar results were observed at day 42. There was no difference between groups in the incidence of adverse events or ocular signs. The total ocular symptoms score was better for T2347 than BPLT upon instillation at day 84 (45.9%/ 44.3%/9.8% of patients with improvement/no change/worsening vs. 33.6%/47.3%/19.1%; P= 0.021), reflecting improvements in individual symptoms such as irritation/burning/stinging (P< 0.001), and itching (P< 0.01) on day 84. Conclusions: Preservative-free latanoprost-timolol fixed combination T2347 showed noninferior efficacy compared with the preserved comparator and was well tolerated.
机译:PRECIS:与含有开口角度胶质瘤或眼高血压患者治疗后84天的含巴卡的制剂相比,对防腐剂的Latanoprost-timolol固定组合证明了疗效的不可效应。目的:本研究的目的是比较对患有开放角青光眼或眼高血压患者的防腐剂 - 无拉坦替代替代药物固定组合(T2347)对苯并氯化铵保存的Latanoprost-Timolol固定组合的影响。方法:III期,随机,并行组,10个国家的投资研究。在第0天随机化,共有242名18岁或以上的患者(60岁或以上的眼睛,在两只眼睛的眼睛,两只眼睛)的眼睛高血压或眼睛高压患者(总体上总体15.7 +/- 2.4mm Hg)进行随机化。期间接收防腐剂替代T2347(n = 127)或保留在保存的比较器(n = 115)上84天。在第4天(+/- 1小时)在第42天和第84天(+/- 1小时)测量从第0天的眼压变化,在第84天统计学地分析T2347至保存比较器的非流动性。还报告了安全参数。结果:从基线到第84天的眼内压力的平均变化为-0.49 +/- 1.80mmHg,用于保存比较器的无防腐剂T2347和-0.49 +/- 2.25mmHg。这些结果符合不可取的限制。在第42天观察到类似的结果。不良事件发生率或眼征的群体之间没有差异。在第84天滴注时,T2347的总眼症状得分比BPLT更好(45.9%/ 44.3%/ 9.8%的改善患者/没有变化/恶化/恶化/恶化/ 47.3%/ 19.1%; P = 0.021),反映各个症状的改善,如刺激/燃烧/刺痛(p <0.001),并在第84天瘙痒(p <0.01)。结论:无防腐拉扎斯托斯 - 蒂莫尔固定组合T2347与保存的比较器相比显示出不可效力耐受良好的。

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