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Study identifier: NCT07441642 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Geographic Atrophy Secondary to Age-related Macular Degeneration  ·  Sponsor: Novartis Pharmaceuticals

PhasePhase 2
Planned participants272
Who can joinAll sexes, 50 Years to no upper limit
Healthy volunteersNo

About this study

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

This description comes directly from the study's public registry record.

Talk to the study team

Novartis Pharmaceuticals  ·  1-888-669-6682  ·  novartis.email@novartis.com

Novartis Pharmaceuticals  ·  +41613241111

Always discuss trial participation with your own doctor first.

Locations (51)

Salehi Retina InstituteHuntington Beach, California, United StatesRecruiting
Retinal Consultants Medical Group IncSacramento, California, United StatesRecruiting
California Retina ConsultantsSanta Barbara, California, United StatesRecruiting
Advanced Research LLCBoynton Beach, Florida, United StatesRecruiting
Advanced Research LLCDeerfield Beach, Florida, United StatesRecruiting
Retina Vitreous Associates of FloridaSt. Petersburg, Florida, United StatesRecruiting
Opthamalic Consultants of BostonBoston, Massachusetts, United StatesRecruiting
NJ RetinaToms River, New Jersey, United StatesRecruiting
New York Eye and Ear Infirmary of Mount SinaiNew York, New York, United StatesRecruiting
Columbia University Medical CenterNew York, New York, United StatesRecruiting
Erie Retina Research LLCErie, Pennsylvania, United StatesRecruiting
Mid Atlantic RetinaPhiladelphia, Pennsylvania, United StatesRecruiting

+ 39 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07441642