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Clinical Trial Summary

This is a parallel, randomized, open-label, controlled study to evaluate the efficacy and safety of oral EG-301 in patients with intermediate non-exudative (dry) age-related macular degeneration (dAMD). Ninety patients will be randomly allocated in a 2:1 ratio to one of two treatment arms for at least 6 months duration. The two treatment arms are: 1. AREDS2 supplements (Control Group, N=30) 2. AREDS2 supplements plus EG-DPMP-01 150 mg daily (Experimental Group, N=60)


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05170048
Study type Interventional
Source Evergreen Therapeutics, Inc.
Contact Xin Du, Ph.D.
Phone 2404064016
Email david.du@egpharm.com
Status Not yet recruiting
Phase Phase 2
Start date September 2024
Completion date September 2025