Phase 3 Study to Assess Efficacy, Safety & Tolerability of OCU410 For Geographic Atrophy Secondary to Dry AMD
What You Need to Know Before You Apply
What is the purpose of this trial?
This study is a Phase 3 multicenter, randomized, controlled, assessor blinded, adaptive study in which subjects will be randomized in a 2:1(OCU410: control) ratio to treatment arm or control arm
Who Is on the Research Team?
Mohamed Genead, MD
Principal Investigator
Ocugen., Inc.
Jennifer Henrick
Principal Investigator
Ocugen., Inc
Are You a Good Fit for This Trial?
What Are the Treatments Tested in This Trial?
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Active Control
OCU410 Single Sub Retinal Injection, 200 µL, 1×10\^10 vg/eye
Control Arm (Untreated)
Find a Clinic Near You
Who Is Running the Clinical Trial?
Ocugen
Lead Sponsor
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