Expired Study
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Norfolk, Virginia 23502


Purpose:

The purpose of this study is to evaluate the safety and efficacy of ocular iontophoresis with dexamethasone phosphate ophthalmic solution EGP-437 using the EyeGate® II Drug Delivery System (EGDS) compared to prednisolone acetate ophthalmic suspension (1%) in patients with non-infectious anterior segment uveitis.


Study summary:

This will be a Phase 3, randomized, double-masked, parallel arm, positive-controlled non-inferiority study, in which up to 250 subjects (approximately 125 subjects per treatment arm) will be enrolled at up to 60 clinical sites. Patients with non-infectious anterior segment uveitis who are interested in participating in the study will be provided an informed consent form prior to screening. Screening/Baseline procedures which include BCVA, slit lamp examination, fundus exam, IOP by tonometry will be used to determine eligibility.


Criteria:

Inclusion Criteria: 1. Age 12 to 85 years with a diagnosis of non-infectious anterior segment uveitis defined as an AC cell count of ≥ 11 cells 2. Receive, understand, and sign a copy of the written informed consent form 3. Be able to return for all study visits and willing to comply with all study-related instructions Exclusion Criteria:


NCT ID:

NCT02517619


Primary Contact:

Principal Investigator
John D. Sheppard, M.D.
Study Principal Investigator


Backup Contact:

N/A


Location Contact:

Norfolk, Virginia 23502
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 18, 2019

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