ABSTRACT
Introduction: Glaucoma is a collection of optic neuropathies consisting of retinal ganglion cell death and corresponding visual field loss. Glaucoma is the leading cause of irreversible vision loss worldwide and is forecasted to precipitously increase in prevalence in the coming decades. Current treatment options aim to lower intraocular pressure (IOP) via topical or oral therapy, laser treatment to the trabecular meshwork or ciliary body, and incisional surgery. Despite increasing use of trabecular laser therapy, topical therapy remains first-line in the treatment of most forms of glaucoma.
Areas covered: Novel glaucoma therapies are a long-standing focus of investigational study. More than two decades have passed since the last United States Food and Drug Administration (FDA) approval of a topical glaucoma drug. Here, the authors review established topical glaucoma drops as well as those currently in FDA phase 2 and 3 clinical trial, nearing clinical use.
Expert opinion: Current investigational glaucoma drugs lower IOP, mainly through enhanced trabecular meshwork outflow. Although few emerging therapies show evidence of retinal ganglion cell and optic nerve neuroprotection in animal models, emerging drugs are focused on lowering IOP, similar to established medicines.
Article highlights
Glaucoma is the most common cause of irreversible vision loss worldwide and is expected to increase in prevalence in the coming decades
Topical therapy of glaucoma is first-line for treatment in most patients
Two decades have passed since the FDA last approved a topical drug for the treatment of glaucoma
Current investigational drugs in phase 2 or phase 3 FDA study show effective intraocular pressure lowering through pathways different than current drugs- namely enhanced trabecular meshwork outflow.
As emerging drugs are still focused on intraocular pressure control, a paradigm shift in the treatment of glaucoma has not yet been realized.
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Declaration of interest
TS Vajaranant has received grants from the NIH, Allergan, Aerie Pharmaceuticals and Bausch & Lomb. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed