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Thursday, September 24, 2015

FDA to Review New Glaucoma Drop Vesneo

When prostaglandin analogue eye drops for glaucoma became available mainstream in the 1990s, they revolutionized glaucoma management and became the first line treatment for most patients. Now Valeant/Bausch and Lomb has submitted a new classification of glaucoma drop treatment to the FDA for fast-track approval: Vesneo, a combination drop of the proven prostaglandin analogue class with the first ever utilization of topical nitric oxide for additional pressure lowering effect.

How aqueous humor travels through the anterior chamber via

Research has proven the effectiveness of nitric oxide in lowering intraocular pressure (IOP) in multiple animal and human studies.  Nitric oxide is a known vasodilator, which can help reduce IOP by decreasing episcleral venous pressure that creates hemodynamic resistance against the flow of aqueous out of the eye. Nitric oxide has an additional benefit of increasing outflow of the aqueous humor through the trabecular meshwork and Schlemm's canal, two of the more prominent drainage structures of the anterior chamber. Prostaglandin analogue category drugs also increase aqueous outflow and drainage, primarily through the uveoscleral pathway (which includes flow across the ciliary muscle and choroid). Theoretically a combination of nitric oxide and prostaglandin analogue medication would cause an additive effect of increased outflow.  Studies suggest that as much as 75% of the aqueous humor outflow occurs through the trabecular meshwork through Schlemm's canal, while the remaining 25% is from other tissue.  That means our most effective glaucoma drop therapy on the market currently (prostaglandin analogues) targets that 25% of outflow, while if we could target trabecular meshwork outflow (like nitric oxide appears to do in studies) we'd be influencing a much larger area of impact.  

No news yet on how much IOP lowering effect we should see from the addition of nitric oxide, but Valeant has targeted a summer 2016 date for FDA testing approval and results should be available at this time.  

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