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 |