Bimatoprost, a synthetic analogue of endogenous prostamides, is in developm
ent as a topical ocular hypotensive agent for the treatment of glaucoma and
ocular hypertension. Prostamides are a newly discovered class of compounds
that have been shown to have potent ocular hypotensive activity in the lab
oratory. Bimatoprost mimics the endogenous prostamides by lowering intraocu
lar pressure (IOP). Bimatoprost provides outstanding control of IOP through
out the day, and a high percentage of patients receiving bimatoprost achiev
e the low target pressures important for clinical success. In controlled cl
inical trials, bimatoprost 0.03% given once daily has displayed efficacy su
perior to timolol 0.5% given twice daily, the current standard for therapy.
Analysis of pooled six month data from two large Phase III trials demonstr
ated that mean IOP was consistently 2 - 3 mmHg lower with bimatoprost q.d.
than with timolol b.i.d. Bimatoprost 0.03% q.d. has also been shown to prov
ide significantly better diurnal IOP control than latanoprost 0.005% q.d.,
probably the most efficacious topical medication currently available. Patie
nts receiving bimatoprost q.d. were more likely than timolol or latanoprost
patients to achieve low target pressures. In all clinical evaluations, bim
atoprost q.d. has been demonstrated to be safe and well-tolerated. Bimatopr
ost will likely be available for clinical use in 2001 and it has great pote
ntial to be superior to all other medications in IOP-lowering efficacy. It
is anticipated that bimatoprost wilt have an important role in therapy for
glaucoma and ocular hypertension.