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J GlaucomaSeptember 20160 citations

Efficacy of Topically Administered Rho-Kinase Inhibitor AR-12286 in Patients With Exfoliation Syndrome and Ocular Hypertension or Glaucoma.

Skaat Alon, Jasien Jessica V, Ritch Robert


AI Summary

AR-12286 eye drops significantly lowered intraocular pressure in exfoliation glaucoma patients, offering a promising new treatment option for this challenging condition.

Abstract

Purpose

To evaluate the efficacy of rho-associated protein kinase inhibitor, AR-12286 topical solution, for its effect in eyes with exfoliation syndrome (XFS) and ocular hypertension (OHT) or exfoliative glaucoma (XFG) and examine any lasting effect on intraocular pressure (IOP) after discontinuation.

Methods

Prospective, double-masked, randomized, interventional study. Patients with XFS and OHT or XFG were enrolled. The study eyes were treated once daily with AR-12286, randomized to 0.5% or 0.7% for 24 weeks. Visits included baseline, 1, 4, and 12 weeks after drug initiation; at 12 weeks AR-12286 was discontinued for 1 week and was resumed at week 13. At the week 24 visit, AR-12286 was discontinued, and a final reexamination was performed at week 25.

Results

Ten patients were treated. Mean baseline IOP was 25±2.4 mm Hg, mean IOP was reduced to 19.1±2.3 mm Hg at 1 week (P<0.001), 17.5±3.6 mm Hg at 4 weeks (P<0.001), and 17.4±3.6 mm Hg at 12 weeks (P<0.001), yielding an average IOP reduction of 23.6%, 30%, and 30.4%, respectively. At the week 13 visit, 1 week after the drug was discontinued, mean IOP increased to 21.6±5.4 mm Hg (P=0.06 compared with baseline visit). At week 24, the mean IOP was 21.8±7.8 mm Hg (P=0.2, and AR-12286 was discontinued). At week 25, the mean IOP was 21.3±5.3 mm Hg (P=0.06).

Conclusions

AR-12286 was well tolerated and provided statistically significant reduction in IOP in patients with XFS and OHT or XFG. This drug may represent an additional therapeutic paradigm for the treatment of XFG.


MeSH Terms

Administration, TopicalAgedAged, 80 and overAntihypertensive AgentsDose-Response Relationship, DrugDouble-Blind MethodExfoliation SyndromeFemaleFollow-Up StudiesGlaucomaHumansIntraocular PressureIsoquinolinesMaleMiddle AgedOcular HypertensionOphthalmic SolutionsProspective StudiesTreatment Outcomerho-Associated Kinases

Key Concepts5

Topically administered Rho-kinase inhibitor AR-12286 reduced mean intraocular pressure (IOP) from a baseline of 25±2.4 mm Hg to 19.1±2.3 mm Hg at 1 week (P<0.001) in 10 patients with exfoliation syndrome and ocular hypertension or exfoliative glaucoma.

TreatmentRCTProspective, double-masked, randomized, interventional studyn=10 patientsCh16Ch29

Topically administered Rho-kinase inhibitor AR-12286 reduced mean intraocular pressure (IOP) from a baseline of 25±2.4 mm Hg to 17.5±3.6 mm Hg at 4 weeks (P<0.001) in 10 patients with exfoliation syndrome and ocular hypertension or exfoliative glaucoma.

TreatmentRCTProspective, double-masked, randomized, interventional studyn=10 patientsCh16Ch29

Topically administered Rho-kinase inhibitor AR-12286 reduced mean intraocular pressure (IOP) from a baseline of 25±2.4 mm Hg to 17.4±3.6 mm Hg at 12 weeks (P<0.001) in 10 patients with exfoliation syndrome and ocular hypertension or exfoliative glaucoma.

TreatmentRCTProspective, double-masked, randomized, interventional studyn=10 patientsCh16Ch29

The average intraocular pressure (IOP) reduction with topically administered Rho-kinase inhibitor AR-12286 was 23.6% at 1 week, 30% at 4 weeks, and 30.4% at 12 weeks in 10 patients with exfoliation syndrome and ocular hypertension or exfoliative glaucoma.

TreatmentRCTProspective, double-masked, randomized, interventional studyn=10 patientsCh16Ch29

After discontinuation of topically administered Rho-kinase inhibitor AR-12286 at week 12, the mean intraocular pressure (IOP) increased to 21.6±5.4 mm Hg at week 13 (1 week after discontinuation, P=0.06 compared with baseline visit) in 10 patients with exfoliation syndrome and ocular hypertension or exfoliative glaucoma.

TreatmentRCTProspective, double-masked, randomized, interventional studyn=10 patientsCh16Ch29

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