At present, medical therapy is the first line of attack against primar
y open-angle glaucoma. beta-blockers, miotics, sympathomimetics, carbo
nic anhydrase inhibitors, and prostaglandins have been used with varyi
ng degrees of success. The alpha(2)-agonists, clonidine, apraclonidine
, and now brimonidine are powerful inhibitors of aqueous humor product
ion, thereby lowering intraocular pressure (IOP) in these patients. Br
imonidine is emerging as a potential first-line therapy for primary op
en-angle glaucoma, with a peak IOP-lowering efficacy comparable to tha
t of timolol, but without timolol's adverse cardiopulmonary side effec
ts. Brimonidine promises to be an important new drug to help meet the
therapeutic challenges faced by ophthalmologists in treating glaucoma.