Last reviewed · How we verify

Latanoprost/Timolol

Universiti Kebangsaan Malaysia Medical Centre · FDA-approved active Small molecule

Latanoprost reduces intraocular pressure by increasing uveoscleral outflow of aqueous humor, while timolol decreases aqueous humor production via beta-adrenergic receptor antagonism.

Latanoprost reduces intraocular pressure by increasing uveoscleral outflow of aqueous humor, while timolol decreases aqueous humor production via beta-adrenergic blockade. Used for Open-angle glaucoma, Ocular hypertension.

At a glance

Generic nameLatanoprost/Timolol
SponsorUniversiti Kebangsaan Malaysia Medical Centre
Drug classProstaglandin analog / Beta-blocker combination
TargetProstaglandin F receptor (FP receptor) / Beta-adrenergic receptors (β1, β2)
ModalitySmall molecule
Therapeutic areaOphthalmology
PhaseFDA-approved

Mechanism of action

Latanoprost is a prostaglandin F2α analog that binds to prostaglandin F receptors on the ciliary muscle, facilitating drainage of fluid from the eye through the unconventional uveoscleral pathway. Timolol is a non-selective beta-blocker that reduces aqueous humor secretion by the ciliary body. Together, these complementary mechanisms provide additive intraocular pressure reduction.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape: