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Clinical trial

A Phase IIa, Randomized, Double-Masked, Placebo-Controlled, Parallel-Group, 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) - PHANTOM Study

NCT05376176 is registered in ClinicalTrials.gov with Santen Inc. as lead sponsor.

NCT NCT05376176
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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase IIa, Randomized, Double-Masked, Placebo-Controlled, Parallel-Group, 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) - PHANTOM Study
Lead sponsor
Santen Inc.
Phase
Phase 2
Overall status
Completed
Start date
May 19, 2022
Completion date
May 26, 2025
Enrollment
86 (actual)
Sites
15

Conditions

As the registry lists them; a condition with its own page is linked.

fuchs endothelial corneal dystrophy