Strohmaier K, Snyder E, DuBiner H, Adamsons I
Department of Clinical Research, Merck Research Laboratories, West Point, Pennsylvania 19486, USA.
Ophthalmology. 1998 Oct;105(10):1936-44. doi: 10.1016/s0161-6420(98)91045-4.
To evaluate whether a fixed combination of 2% dorzolamide and 0.5% timolol given twice daily showed equivalent efficacy to the concomitant administration of 2% dorzolamide given three times daily and 0.5% timolol given twice daily in patients whose intraocular pressure (IOP) remained elevated during monotherapy with 0.5% timolol twice daily.
Multicenter, parallel, randomized, double-masked clinical trial with an open-label extension.
In the masked phase, 242 patients received either the dorzolamide-timolol combination twice daily and placebo three times daily or dorzolamide three times daily and timolol twice daily for up to 3 months. In the open-label extension, 220 patients received the dorzolamide-timolol combination twice daily for up to 9 months.
The criterion for establishing treatment equivalency was a 95% or greater confidence that the absolute difference in the mean change in IOP from baseline was less than 1.5 mmHg between treatments.
During 3 months of treatment, the dorzolamide-timolol combination reduced IOP relative to the 0.5% timolol baseline by approximately 14% at hour 0 (just before the morning dose), 20% at hour 2, and 15% at hour 8. The IOP-lowering effect of concomitant therapy with dorzolamide and timolol was approximately 16% at hour 0.20% at hour 2, and 17% at hour 8. At hours 0, 2, and 8, there was greater than 97% confidence that the treatments were equivalent. During the open-label extension, the mean IOP reduction ranged from 14% to 15% at hour 0 and from 20% to 21% at hour 2. The treatment groups were generally comparable in terms of adverse events, symptoms, ocular signs, visual acuity, visual fields, physical examination, and laboratory measures.
The IOP-lowering effect of the dorzolamide-timolol combination is comparable to that of dorzolamide three times daily plus timolol twice daily and is maintained for up to 1 year. The dorzolamide-timolol combination provides clinically important reduction in IOP relative to baseline treatment with timolol alone and is generally well-tolerated for up to 1 year.
评估对于每日两次使用0.5%噻吗洛尔单药治疗期间眼压(IOP)仍升高的患者,每日两次给予2%多佐胺和0.5%噻吗洛尔的固定复方制剂,其疗效是否等同于每日三次给予2%多佐胺和每日两次给予0.5%噻吗洛尔的联合用药。
多中心、平行、随机、双盲临床试验,并进行开放标签扩展。
在双盲阶段,242例患者接受每日两次多佐胺 - 噻吗洛尔复方制剂和每日三次安慰剂,或每日三次多佐胺和每日两次噻吗洛尔,治疗长达3个月。在开放标签扩展阶段,220例患者接受每日两次多佐胺 - 噻吗洛尔复方制剂,治疗长达9个月。
确立治疗等效性的标准是,治疗组间眼压从基线变化的均值绝对差异小于1.5 mmHg的置信度达到95%或更高。
在3个月的治疗期间,多佐胺 - 噻吗洛尔复方制剂相对于0.5%噻吗洛尔基线,在0小时(早晨给药前)使眼压降低约14%,2小时时降低20%,8小时时降低15%。多佐胺和噻吗洛尔联合治疗的降眼压效果在0小时约为16%,2小时时为20%,8小时时为17%。在0、2和8小时,治疗等效的置信度大于97%。在开放标签扩展阶段,0小时眼压平均降低幅度为14%至15%,2小时时为20%至21%。治疗组在不良事件、症状、眼部体征、视力、视野、体格检查和实验室指标方面总体相当。
多佐胺 - 噻吗洛尔复方制剂的降眼压效果与每日三次多佐胺加每日两次噻吗洛尔的联合用药相当,且可维持长达1年。相对于单独使用噻吗洛尔的基线治疗,多佐胺 - 噻吗洛尔复方制剂可使眼压在临床上显著降低,并且在长达1年的时间内通常耐受性良好。