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Netarsudil

Alternative Names: netarsudil, rhopressa, ar-13324, ar 13324, ar13324, rocklatan
Latest Update: 2024-11-25
Latest Update Note: Clinical Trial Update

Product Description

Netarsudil ophthalmic is used to treat glaucoma (a condition in which increased pressure in the eye can lead to gradual loss of vision) and ocular hypertension (a condition which causes increased pressure in the eye). Netarsudil is in a class of medications called rho kinase inhibitors. It works by lowering the pressure in the eye by increasing the flow of natural eye fluids out of the eye.

Mechanisms of Action: ROCK Inhibitor

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Topical,Ophthalmic

FDA Designation: None *

Approval Status: Approved

Approved Countries: Austria | Bangladesh | Belgium | Croatia | Czech | Denmark | Estonia | European Medicines Agency | Finland | Germany | Hungary | Iceland | India | Ireland | Italy | Korea | Latvia | Lithuania | Netherlands | Norway | Poland | Portugal | Slovakia | Sweden | United Arab Emirates | United Kingdom | United States

Approved Indications: Hypertension | Glaucoma | Glaucoma, Open-Angle

Known Adverse Events: Hyperemia | Pain Unspecified

Company: Alcon
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Netarsudil

Countries in Clinic: Japan, United States

Active Clinical Trial Count: 3

Highest Development Phases

Phase 3: Glaucoma|Hypertension

Phase 2: Glaucoma, Open-Angle

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

GLR305-E001

P2

Recruiting

Glaucoma, Open-Angle|Hypertension

2025-11-01

jRCT2031210125

P3

Recruiting

Glaucoma

2025-03-31

jRCT2031210122

P3

Completed

Glaucoma|Hypertension

2022-05-02

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