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Emixustat

Alternative Names: emixustat, acu-4429
Latest Update: 2024-05-30
Latest Update Note: Clinical Trial Update

Product Description

Mechanisms of Action: RPE65 Inhibitor

Novel Mechanism: Yes

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: Orphan Drug - Stargardt Disease *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Kubota Vision
Company Location:
Company CEO:
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 3: Geographic Atrophy|Macular Degeneration|Stargardt Disease

Phase 2: Macular Degeneration|Geographic Atrophy|Stargardt Disease|Anetoderma|Diabetic Retinopathy

Phase 1: Healthy Volunteers|Geographic Atrophy|Macular Degeneration

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

The SeaSTAR Study (Safety and efficacy of EmixustAt in STARgardt disease)

P3

Unknown status

Stargardt Disease

2022-11-18

SeaSTAR

P3

Completed

Macular Degeneration|Stargardt Disease

2022-06-13

NCT02753400

P2

Completed

Diabetic Retinopathy

2017-11-01

NCT03033108

P2

Completed

Anetoderma|Stargardt Disease|Macular Degeneration

2017-11-01

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