drugset / Trial / NCT07441642

A Study to Investigate Efficacy and Safety of FWY003 Compared With Placebo in Participants With Geographic Atrophy Secondary to Age-related Macular Degeneration

NCT07441642 ↗

Phase 2 Recruiting 272 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupDouble-blindTreatment

Summary

To characterize the dose response relationship of FWY003 in participants with geographic atrophy (GA) secondary to age-related macular degeneration (AMD).

Timeline

Start
2026-03-09
Primary completion
2029-08-21
Completion
2029-08-22

Drugs

EvaluationDrugModalityDoseRoute
Subject FWY003 Unknown — —