Trial Profile

A Phase 2, Parallel, Randomized, Open-label, Controlled Study of EG-301 150 mg Daily in Patients With Nonfocal Geographic Atrophy Secondary to Dry-AMD

Status: Not yet recruiting

Phase of Trial: Phase II

Latest Information Update: 08 Jan 2026

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At a glance

Drugs EG 301 (Primary) ; Ascorbic acid/betacarotene/copper(II) oxide/tocopherol/zinc oxide
Indications Dry macular degeneration
Focus Adverse reactions; Therapeutic Use
Sponsors Evergreen Therapeutics

Most Recent Events

08 Dec 2025 Planned End Date changed from 1 Jun 2026 to 1 Jun 2028.
08 Dec 2025 Planned primary completion date changed from 1 Jun 2026 to 1 Jun 2028.
08 Dec 2025 Planned initiation date changed from 1 Jun 2025 to 1 Jun 2026.

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