4.2 Article

The Effects of Netarsudil Ophthalmic Solution on Aqueous Humor Dynamics in a Randomized Study in Humans

Journal

JOURNAL OF OCULAR PHARMACOLOGY AND THERAPEUTICS
Volume 34, Issue 5, Pages 380-386

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/jop.2017.0138

Keywords

netarsudil; glaucoma; aqueous humor dynamics; outflow

Funding

  1. Aerie Pharmaceuticals, Inc. (Bedminster, NJ)

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Purpose: Netarsudil, an inhibitor of Rho kinase and a norepinephrine transporter, has been shown to lower elevated intraocular pressure (IOP) in controlled studies of patients with open-angle glaucoma and ocular hypertension, and in healthy volunteers. The mechanism of this ocular hypotensive effect in humans is unknown. Methods: The objective of this study was to evaluate the effect of netarsudil 0.02% on aqueous humor dynamics (AHD) parameters. In this double-masked, vehicle-controlled, paired-eye comparison study, 11 healthy volunteers received topical netarsudil ophthalmic solution 0.02% or its vehicle once daily for 7 days (morning dosing). The primary endpoints were the change in AHD parameters, compared between active and vehicle-treated eyes. Results: In netarsudil-treated eyes, diurnal outflow facility increased from 0.270.10L/min/mmHg to 0.33 +/- 0.11L/min/mmHg (+22%; P=0.02) after 7 days of treatment. In placebo-treated eyes, diurnal outflow facility did not significantly change (P=0.94). The difference between netarsudil and placebo eyes in diurnal change of outflow facility was 0.08L/min/mmHg (P<0.001). Diurnal episcleral venous pressure (EVP) in netarsudil-treated eyes decreased from 7.9 +/- 1.2mmHg to 7.2 +/- 1.8 (-10%; P=0.01). Diurnal EVP was not significantly different between netarsudil- and placebo-treated eyes. There was a trend toward decreasing aqueous humor flow rate (-15%; P=0.08). No treatment changes were seen in uveoscleral outflow rate. Conclusions and Relevance: Once-daily dosing of netarsudil ophthalmic solution 0.02% lowered IOP through increasing trabecular outflow facility and reducing EVP. This suggests a combination of mechanisms that affect both the proximal and distal outflow pathways.

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