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Brand-name latanoprost

CHU de Quebec-Universite Laval · FDA-approved active Small molecule

Latanoprost is a prostaglandin F analog that binds to the prostaglandin F (FP) receptor to increase uveoscleral outflow of aqueous humor, thereby lowering intraocular pressure.

Latanoprost is a prostaglandin F analog that binds to the prostaglandin F (FP) receptor to increase uveoscleral outflow of aqueous humor, thereby lowering intraocular pressure. Used for Open-angle glaucoma, Ocular hypertension.

At a glance

Generic nameBrand-name latanoprost
Also known asXalatan
SponsorCHU de Quebec-Universite Laval
Drug classProstaglandin F analog
TargetFP prostaglandin receptor
ModalitySmall molecule
Therapeutic areaOphthalmology
PhaseFDA-approved

Mechanism of action

Latanoprost acts as a selective agonist at the FP prostaglandin receptor in the eye. By activating this receptor, it enhances drainage of aqueous humor through the uveoscleral (unconventional) pathway, which is the primary mechanism for reducing intraocular pressure. This reduction in IOP helps prevent or slow progression of glaucomatous damage.

Approved indications

Common side effects

Key clinical trials

Primary sources

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

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