INTRAOCULAR PRESSURE-REDUCING EFFECT OF PHXA41 IN PATIENTS WITH INCREASED EYE PRESSURE - A ONE-MONTH STUDY

Citation
A. Alm et al., INTRAOCULAR PRESSURE-REDUCING EFFECT OF PHXA41 IN PATIENTS WITH INCREASED EYE PRESSURE - A ONE-MONTH STUDY, Ophthalmology, 100(9), 1993, pp. 1312-1317
Citations number
16
Categorie Soggetti
Ophthalmology
Journal title
ISSN journal
01616420
Volume
100
Issue
9
Year of publication
1993
Pages
1312 - 1317
Database
ISI
SICI code
0161-6420(1993)100:9<1312:IPEOPI>2.0.ZU;2-9
Abstract
Purpose: To establish the dose-response relationship for the effect on intraocular pressure (IOP) and side effects during long-term treatmen t of patients with ocular hypertension with the prostaglandin F2alpha (PGF2alpha) analog PhXA41. Methods: A three-center, randomized, double -masked study where IOP, conjunctival hyperemia, and ocular irritation were followed during a 1 -month twice-daily treatment with placebo or 35, 60, or 115 mug/ml PhXA41 in 60 patients with ocular hypertension, primary open-angle glaucoma, or capsular glaucoma. Results: The three concentrations of PhXA41 reduced the average IOP between 31% and 38% during the second day of treatment, with only a weak dose-response rel ationship. The initial effect declined somewhat during the first 2 wee ks of treatment but then remained at the same level for the rest of th e study, with a pressure reduction of approximately 20% for all three concentrations. On the second day of treatment, mild conjunctival hype remia could be observed in most treated patients. Nineteen of 45 PhXA4 1 -treated patients, compared with 2 of 15 placebo-treated patients, r eported to have mild to moderate ocular irritation. These side effects became less pronounced during the study, and at the end there was lit tle difference in the degree of conjunctival hyperemia between placebo - and drug-treated eyes, and no drug-related ocular irritation was rep orted with the two lowest concentrations of PhXA41. Conclusions: It is confirmed that the PGF2alpha analog PhXA41 is a major improvement wit h respect to the effect-side effect relationship and that it may becom e a valuable new agent for the treatment of glaucoma.