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Ripasudil

Alternative Names: ripasudil, k-321, k321, k 321, glanatec
Latest Update: 2024-11-05
Latest Update Note: Clinical Trial Update

Product Description

Ripasudil hydrochloride hydrate (Glanatec ophthalmic solution 0.4 %; hereafter referred to as ripasudil) is a small-molecule, Rho-associated kinase inhibitor developed by Kowa Company, Ltd. for the treatment of glaucoma and ocular hypertension.

Mechanisms of Action: ROCK Inhibitor

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Ocular,Ophthalmic

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: India | Japan | Korea | Malaysia | Singapore

Approved Indications: None

Known Adverse Events: None

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

Clinical Description

Map of Global Clinical Trials for Ripasudil

Countries in Clinic: Canada, Denmark, Germany, Puerto Rico, Spain, United Kingdom, United States

Active Clinical Trial Count: 7

Highest Development Phases

Phase 3: Blindness|Capsule Opacification|Cataract|Corneal Dystrophies, Hereditary|Corneal Edema|Corneal Endothelial Cell Loss|Diabetic Retinopathy|Fuchs' Endothelial Dystrophy

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

K-321-301

P3

Unknown Status

Diabetic Retinopathy

2025-08-30

RDMEK-01

P2

Recruiting

Fuchs' Endothelial Dystrophy

2025-02-01

FECD

P3

Recruiting

Corneal Dystrophies, Hereditary|Fuchs' Endothelial Dystrophy

2024-12-01

FECD

P3

Active, not recruiting

Fuchs' Endothelial Dystrophy|Cataract|Corneal Dystrophies, Hereditary

2024-10-01

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