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travoprost 0.004% (drug)

University Hospital, Basel, Switzerland · FDA-approved active Small molecule

travoprost 0.004% (drug) is a Prostaglandin F analog Small molecule drug developed by University Hospital, Basel, Switzerland. It is currently FDA-approved for Open-angle glaucoma, Ocular hypertension.

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

Travoprost 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 nametravoprost 0.004% (drug)
SponsorUniversity Hospital, Basel, Switzerland
Drug classProstaglandin F analog
TargetProstaglandin F receptor (FP receptor)
ModalitySmall molecule
Therapeutic areaOphthalmology
PhaseFDA-approved

Mechanism of action

Travoprost 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 uveoscleral (unconventional) pathway, leading to decreased intraocular pressure. The drug is selective for the FP receptor and does not significantly activate other prostaglandin receptors.

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

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Frequently asked questions about travoprost 0.004% (drug)

What is travoprost 0.004% (drug)?

travoprost 0.004% (drug) is a Prostaglandin F analog drug developed by University Hospital, Basel, Switzerland, indicated for Open-angle glaucoma, Ocular hypertension.

How does travoprost 0.004% (drug) work?

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

What is travoprost 0.004% (drug) used for?

travoprost 0.004% (drug) is indicated for Open-angle glaucoma, Ocular hypertension.

Who makes travoprost 0.004% (drug)?

travoprost 0.004% (drug) is developed and marketed by University Hospital, Basel, Switzerland (see full University Hospital, Basel, Switzerland pipeline at /company/university-hospital-basel-switzerland).

What drug class is travoprost 0.004% (drug) in?

travoprost 0.004% (drug) belongs to the Prostaglandin F analog class. See all Prostaglandin F analog drugs at /class/prostaglandin-f-analog.

What development phase is travoprost 0.004% (drug) in?

travoprost 0.004% (drug) is FDA-approved (marketed).

What are the side effects of travoprost 0.004% (drug)?

Common side effects of travoprost 0.004% (drug) include Conjunctival hyperemia, Iris pigmentation increase, Eyelash growth (hypertrichosis), Eye irritation/discomfort, Periocular skin pigmentation.

What does travoprost 0.004% (drug) target?

travoprost 0.004% (drug) targets Prostaglandin F receptor (FP receptor) and is a Prostaglandin F analog.

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