Study to Assess Safety and Tolerability of Multiple Doses of EO2002

Recruiting Phase 1 Interventional Study
Corneal Edema Corneal Endothelial Dystrophy Endothelial Dysfunction Fuchs Dystrophy Fuchs' Endothelial Dystrophy Bullous Keratopathy Pseudophakic Bullous Keratopathy Corneal Edema Pseudophakic
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 1
Study type
Interventional
Purpose
Treatment
Participants needed
12 (estimated)
Sponsor
Asociación para Evitar la Ceguera en México · Other
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About This Trial

The goal of this clinical study is to assess the safety of multiple intracameral injections of EO2002 with and without topical Ripasudil.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: All ocular criteria apply to the study eye unless otherwise noted. 1. Age ≥ 18 years. 2. Subject is phakic or pseudophakic with a posterior chamber intraocular lens (lens in the bag or sulcus). 3. Symptomatic corneal edema associated with endothelial dysfunction which may be se…
Contacts

Yara Luna

55 39 53 12 25

reclutamiento.proyectos@apec.com.mx

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