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Preservative-Free Tafluprost

Merck Sharp & Dohme LLC · Phase 3 active Small molecule

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

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

At a glance

Generic namePreservative-Free Tafluprost
Also known asMK2452
SponsorMerck Sharp & Dohme LLC
Drug classProstaglandin F analog
TargetProstaglandin F receptor (FP receptor)
ModalitySmall molecule
Therapeutic areaOphthalmology
PhasePhase 3

Mechanism of action

Tafluprost mimics the action of prostaglandin F by activating FP receptors on the ciliary muscle bundle and trabecular meshwork. This activation enhances drainage of aqueous humor through the unconventional (uveoscleral) pathway, leading to decreased intraocular pressure. The preservative-free formulation aims to reduce ocular surface irritation and improve tolerability in patients requiring chronic topical therapy.

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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