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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

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Trial Profile

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

Status: Active, no longer recruiting
Phase of Trial: Phase II

Latest Information Update: 20 May 2024

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At a glance

  • Drugs AE 001 (Primary)
  • Indications Fuchs' endothelial dystrophy
  • Focus Proof of concept; Therapeutic Use
  • Acronyms PHANTOM
  • Sponsors Santen Inc

Most Recent Events

  • 13 May 2024 Planned End Date changed from 1 Mar 2025 to 30 May 2025.
  • 13 May 2024 Planned primary completion date changed from 1 Mar 2025 to 30 May 2025.
  • 13 May 2024 Status changed from recruiting to active, no longer recruiting.

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