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Bimatoprost · Durysta, Latisse

Small molecule · Modulator · developed by Abbvie

Approved FDA, Mar 2001
2 Registered trials

What is Bimatoprost?

Bimatoprost is a synthetic prostaglandin analog with ocular hypotensive activity. It is believed to lower intraocular pressure by increasing aqueous humor outflow through both the trabecular meshwork and uveoscleral routes.

Summary written with AI from the sources listed at the end of this page.

At a glance

Also known as
Durysta, Latisse, Lumigan, Zolymbus, AGN-192024
Drug type
Small molecule
Mechanism
Modulator
Pathways
aqueous humor outflow through trabecular meshwork and uveoscleral routes
Therapy area
Ophthalmology
Developer
Abbvie
In trials of
AMRX
FDA status
Approved as Durysta, Latisse, Lumigan (March 16, 2001), NDA021275 · FDA label
UNII
QXS94885MZ

✅ FDA-approved uses

From the indications section of the FDA label (version of Feb 25, 2026). Read the full label for the exact wording, limitations and safety information.

🧪 Clinical trials

TrialPhaseConditionStatusSponsor
NCT05401357 Phase 3 Glaucoma, Open-Angle Recruiting AMRX
NCT06267274 Phase 1 Open-angle Glaucoma Unknown AMRX

Trials of the companies BioRadar tracks, from ClinicalTrials.gov, most advanced phase first.

Conditions studied

Glaucoma, Open-AngleOcular HypertensionOpen-angle Glaucoma

Sources

Updated Oct 11, 2026.

Data: FDA (Drugs@FDA, Purple Book, DailyMed), NIH (NCI Thesaurus, GSRS, RxNorm), ClinicalTrials.gov • Informational purposes only, not medical or investment advice. • All drugs A–Z

This data is for informational purposes only, not investment advice. BioRadar does not provide buy/sell recommendations. Past performance does not guarantee future results. Always do your own due diligence.