Cs. Foster et al., EFFICACY AND SAFETY OF RIMEXOLONE 1-PERCENT OPHTHALMIC SUSPENSION VS 1-PERCENT PREDNISOLONE ACETATE IN THE TREATMENT OF UVEITIS, American journal of ophthalmology, 122(2), 1996, pp. 171-182
PURPOSE: Two multicenter studies compared the efficacy and safety of r
imexolone 1% ophthalmic suspension (Vexol 1%, Alcon) and 1% prednisolo
ne acetate (Pred Forte, Allergan). METHODS: Patients with acute uveiti
s, recurrent iridocyclitis, or chronic uveitis treatable by topical co
rticosteroid were enrolled, Treatment regimen was one or two drops eve
ry hour during Week 1, every two hours during Week 2, four times a day
during Week 3, and once a day for the last three days, Efficacy and s
afety were determined on Days 3, 4, 7 to 10, 14, 21, and 28, A poststu
dy evaluation was conducted 36 to 72 hours after treatment was stopped
. RESULTS: When anterior chamber cell and flare were measured, rimexol
one 1% was found to be as effective as 1% prednisolone. The largest di
fference observed between treatments was 0.5 score unit, not clinicall
y significant, There were no statistically significant differences in
cell scores in either study (P > .05), No statistically significant di
fferences in flare scores were found except at Day 28 in Study One (P
= .04). Also, prednisolone was found to be more likely than rimexolone
to cause a clinically significant increase (10 mm Hg or more) in intr
aocular pressure (1.7 times more likely in Study One, eight times more
likely in Study Two). CONCLUSION: Rimexolone 1% ophthalmic suspension
is safe and effective for the treatment of uveitis.