A prospective, randomized, single-masked study evaluating the ocular efficacy and safety of two doses of the EYP-1901 intravitreal insert compared to aflibercept
A study to evaluate Efficacy and Safety of two doses of EYP-1901 in subjects with DME
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
27
Intravitreal Injection
Intravitreal Injection
EyePoint Investigative Site
Phoenix, Arizona, United States
EyePoint Investigative Site
Lemont, Illinois, United States
EyePoint Investigative Site
Hagerstown, Maryland, United States
EyePoint Investigative Site
Reno, Nevada, United States
Time to first supplemental aflibercept injection following EYP-1901 dose at Baseline vs Aflibercept
Timing of supplemental injection
Time frame: Week 24
Change in best corrected visual acuity (BCVA)
Changes in BCVA
Time frame: Week 24
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EyePoint Investigative Site
Erie, Pennsylvania, United States
EyePoint Investigative Site
Lynchburg, Virginia, United States