Atlas Trials

A Multicenter Study Assessing the Efficacy and Safety of STN1010904 Ophthalmic Suspension 0.03% and 0.1% Compared With Vehicle in Subjects With Fuchs Endothelial Corneal Dystrophy (FECD)

Clinical trial NCT05376176 · COMPLETED

Trial details

NCT number
NCT05376176
Sponsor
Santen Inc.
Status
COMPLETED
Phase
Phase 2
Study type
INTERVENTIONAL
Fuchs Endothelial Corneal Dystrophy
Start date
2022-05-19
Primary completion
2025-05-26
Enrollment
86

View on ClinicalTrials.gov

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