Hofmann H M, Feicht B, Brunner-Ferber E, Lippa E, von Denffer H
Augenklinik und Poliklinik, Klinikum rechts der Isar, Technischen Universität, München, Bundesrepublik Deutschland.
Fortschr Ophthalmol. 1991;88(5):513-4.
A three-dose, randomized, double-blind parallel, placebo-controlled ocular tolerancy study was undertaken in 24 healthy, normal volunteers with two formulations of 2% MK-507 (L-671 152), a novel water-soluble, topical carbonic anhydrase inhibitor. In this study MK-507 was administered to humans for the first time. Subjects received 3 sequential drops of the test drug in one randomly selected eye (at 13:00, 14:00, and 14:10 o'clock): ten received 2% MK-507 formulated with 0.5% hydroxyethylcellulose (HEC); ten, 2% MK-507 with no HEC; two, vehicle with HEC; and two, vehicle without HEC. Local tolerance of 2% MK-507 was good with predominantly mild and transient local symptoms, somewhat fewer for the formulation without HEC. Significant lowering of intraocular pressure (IOP) by up to 7 mmHg was noted when comparing IOP 4 h and 5 h after the first dose with IOP 20 h and 19 h before the first dose in the treated eyes of subjects receiving MK-507. Slightly greater activity was noted when MK-507 was formulated with HEC.
一项三剂量、随机、双盲平行、安慰剂对照的眼部耐受性研究在24名健康的正常志愿者中开展,使用了两种2% MK-507(L-671 152)制剂,这是一种新型水溶性局部碳酸酐酶抑制剂。在本研究中,MK-507首次应用于人体。受试者在一只随机选择的眼睛中依次滴入3滴受试药物(分别于13:00、14:00和14:10):10人接受含0.5%羟乙基纤维素(HEC)的2% MK-507制剂;10人接受不含HEC的2% MK-507制剂;2人接受含HEC的赋形剂;2人接受不含HEC的赋形剂。2% MK-507的局部耐受性良好,主要为轻度和短暂的局部症状,不含HEC的制剂症状略少。在接受MK-507的受试者的受试眼中,将首次给药后4小时和5小时的眼压与首次给药前20小时和19小时的眼压进行比较时,发现眼压显著降低高达7 mmHg。当MK-507与HEC一起配制时,观察到活性略高。