TY - JOUR
T1 - Netarsudil Improves Trabecular Outflow Facility in Patients with Primary Open Angle Glaucoma or Ocular Hypertension
T2 - A Phase 2 Study
AU - Sit, Arthur J.
AU - Gupta, Divakar
AU - Kazemi, Arash
AU - McKee, Hayley
AU - Challa, Pratap
AU - Liu, Katy C.
AU - Lopez, Jae
AU - Kopczynski, Casey
AU - Heah, Theresa
N1 - Funding Information:
ALL AUTHORS HAVE COMPLETED AND SUBMITTED THE ICMJE FORM FOR DISCLOSURE OF POTENTIAL CONFLICTS OF INTEREST. Funding/Support: This work was funded by Aerie Pharmaceuticals, Inc. Durham, NC, which designed and conducted the study including data collection, management, and interpretation, as well as preparation, review, and approval of the manuscript. Financial Disclosures: Arthur J. Sit receives research support from Aerie Pharmaceuticals; and has a personal financial interest in Injectsense; and is a consultant for Aerie Pharmaceuticals, Allergan, Bausch Health, Injectsense, and PolyActiva. Pratap Challa owns stock in Aerie Pharmaceuticals. Theresa Heah is an employee of AsclepiX Therapeutics, and was an employee of Aerie Pharmaceuticals, at the time of the study. Divakar Gupta, Arash Kazemi, and Katy C. Liu have no disclosures to report. Acknowledgements: Medical writing and editorial assistance were provided by BioScience Communications, New York, New York, funded by Aerie Pharmaceuticals, Inc.
Funding Information:
Acknowledgements: Medical writing and editorial assistance were provided by BioScience Communications, New York, New York, funded by Aerie Pharmaceuticals, Inc.
Publisher Copyright:
© 2021 The Authors
PY - 2021/6
Y1 - 2021/6
N2 - Purpose: Intraocular pressure (IOP) reduction is key to controlling primary open angle glaucoma (POAG). Pharmacotherapies for POAG or ocular hypertension (OHT) commonly lower IOP by increasing uveoscleral outflow or decreasing aqueous humor production. Netarsudil (Rhopressa), a Rho kinase inhibitor, reduces IOP by improving trabecular outflow facility, which is reduced in POAG. We investigated the effects of netarsudil on aqueous humor dynamics in patients with POAG or OHT. Design: Double-masked, randomized, vehicle-controlled, Phase 2 trial. Methods: Netarsudil 0.02% was instilled in 1 eye and vehicle into the contralateral eye of 20 patients once daily in the morning for 7 days. The primary endpoint was change in mean diurnal outflow facility on day 8 versus that on day 1 (baseline). Outflow facility was measured by using Schiøtz tonography, IOP by pneumotonometry, and episcleral venous pressure (EVP) by automated venomanometry. Results: Eighteen patients (90%) completed the study. Mean diurnal outflow facility increased 0.039 versus 0.007 µL/min/mm Hg from baseline in the netarsudil- and the vehicle-treated groups, respectively (P < .001 vs. baseline for netarsudil), a treatment difference of 0.03 µL/min/mm Hg (P ≤. 001). Mean diurnal IOP change from baseline at day 8 was −4.52 mm Hg for netarsudil versus −0.98 mm Hg for vehicle, a treatment difference of −3.54 mm Hg (P < .0001). Mean diurnal EVP change from baseline was −0.79 mm Hg in the netarsudil-treated group versus 0.10 mm Hg for vehicle, a treatment difference of −0.89 mm Hg (P < .001). All patients reporting an adverse event reported conjunctival hyperemia of mild or moderate severity. Conclusions: Netarsudil acts on the conventional outflow pathway, both proximal and distal, to significantly reduce IOP in POAG and OHT by improving trabecular outflow facility and decreasing EVP.
AB - Purpose: Intraocular pressure (IOP) reduction is key to controlling primary open angle glaucoma (POAG). Pharmacotherapies for POAG or ocular hypertension (OHT) commonly lower IOP by increasing uveoscleral outflow or decreasing aqueous humor production. Netarsudil (Rhopressa), a Rho kinase inhibitor, reduces IOP by improving trabecular outflow facility, which is reduced in POAG. We investigated the effects of netarsudil on aqueous humor dynamics in patients with POAG or OHT. Design: Double-masked, randomized, vehicle-controlled, Phase 2 trial. Methods: Netarsudil 0.02% was instilled in 1 eye and vehicle into the contralateral eye of 20 patients once daily in the morning for 7 days. The primary endpoint was change in mean diurnal outflow facility on day 8 versus that on day 1 (baseline). Outflow facility was measured by using Schiøtz tonography, IOP by pneumotonometry, and episcleral venous pressure (EVP) by automated venomanometry. Results: Eighteen patients (90%) completed the study. Mean diurnal outflow facility increased 0.039 versus 0.007 µL/min/mm Hg from baseline in the netarsudil- and the vehicle-treated groups, respectively (P < .001 vs. baseline for netarsudil), a treatment difference of 0.03 µL/min/mm Hg (P ≤. 001). Mean diurnal IOP change from baseline at day 8 was −4.52 mm Hg for netarsudil versus −0.98 mm Hg for vehicle, a treatment difference of −3.54 mm Hg (P < .0001). Mean diurnal EVP change from baseline was −0.79 mm Hg in the netarsudil-treated group versus 0.10 mm Hg for vehicle, a treatment difference of −0.89 mm Hg (P < .001). All patients reporting an adverse event reported conjunctival hyperemia of mild or moderate severity. Conclusions: Netarsudil acts on the conventional outflow pathway, both proximal and distal, to significantly reduce IOP in POAG and OHT by improving trabecular outflow facility and decreasing EVP.
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U2 - 10.1016/j.ajo.2021.01.019
DO - 10.1016/j.ajo.2021.01.019
M3 - Article
C2 - 33524367
AN - SCOPUS:85104130402
SN - 0002-9394
VL - 226
SP - 262
EP - 269
JO - American Journal of Ophthalmology
JF - American Journal of Ophthalmology
ER -