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Preservative-free latanoprost

Association for Innovation and Biomedical Research on Light and Image · FDA-approved active Small molecule

Latanoprost is a prostaglandin F analog that binds to prostaglandin F receptors in the eye to increase uveoscleral outflow of aqueous humor, thereby lowering intraocular pressure.

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

At a glance

Generic namePreservative-free latanoprost
Also known asMonoprost
SponsorAssociation for Innovation and Biomedical Research on Light and Image
Drug classProstaglandin F analog
TargetProstaglandin F receptor (FP receptor)
ModalitySmall molecule
Therapeutic areaOphthalmology
PhaseFDA-approved

Mechanism of action

Latanoprost mimics the action of prostaglandin F2α by activating FP receptors on the ciliary muscle bundle and trabecular meshwork. This increases unconventional (uveoscleral) drainage of aqueous humor from the anterior chamber, reducing intraocular pressure. The preservative-free formulation eliminates potential irritation from benzalkonium chloride or other preservatives, improving tolerability in sensitive eyes.

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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