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Travoprost and Timolol

Afyon Kocatepe University Hospital · FDA-approved active Small molecule

Travoprost is a prostaglandin F analog that increases uveoscleral outflow of aqueous humor, while timolol is a non-selective beta-blocker that decreases aqueous humor production, together reducing intraocular pressure.

Travoprost is a prostaglandin F analog that increases uveoscleral outflow of aqueous humor, while timolol is a non-selective beta-blocker that decreases aqueous humor production, together reducing intraocular pressure. Used for Open-angle glaucoma, Ocular hypertension.

At a glance

Generic nameTravoprost and Timolol
Also known asTravoprost 0.004%/timolol 0.5% fixed combination
SponsorAfyon Kocatepe University Hospital
Drug classProstaglandin analog and beta-blocker combination
TargetFP receptor (travoprost); beta-2 adrenergic receptor (timolol)
ModalitySmall molecule
Therapeutic areaOphthalmology
PhaseFDA-approved

Mechanism of action

Travoprost binds to prostaglandin F (FP) receptors on the ciliary muscle and trabecular meshwork, enhancing drainage of aqueous humor through the uveoscleral pathway. Timolol blocks beta-2 adrenergic receptors in the ciliary body, reducing aqueous humor secretion. The combination provides additive intraocular pressure-lowering effects through complementary mechanisms.

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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