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Study identifier: NCT06961370 Synced from ClinicalTrials.gov · August 05, 2026
● Completed

A Study to Investigate Safety, Tolerability, Pharmacokinetics (PK), Pharmacodynamics (PD), and Immunogenicity of RO7669330 in Participants With Geographic Atrophy (GA) Secondary to Age-related Macular Degeneration (AMD)

Condition: Geographic Atrophy · Age-related Macular Degeneration  ·  Sponsor: Hoffmann-La Roche

PhasePhase 1
Planned participants27
Who can joinAll sexes, 55 Years to no upper limit
Healthy volunteersNo

About this study

The main purpose of this study is to assess the ocular and systemic safety and tolerability of RO7669330 in participants with GA secondary to AMD in at least one eye in Part 1, or both eyes in Part 2, after multiple unilateral intravitreal (IVT) doses.

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

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Locations (17)

Associated Retina Consultants - Phoenix - DocTrials - PPDSPhoenix, Arizona, United States
Barnet Dulaney Perkins Eye CenterSun City, Arizona, United States
Retina-Vitreous Associates Medical GroupBeverly Hills, California, United States
Global Research ManagementGlendale, California, United States
Retinal Consultants Medical Group Inc - Parkcenter DriveSacramento, California, United States
Southeast Retina CenterAugusta, Georgia, United States
Cumberland Valley Retina Consultants PCHagerstown, Maryland, United States
Deep Blue Retina Clinical ResearchSouthaven, Mississippi, United States
The Retina InstituteSt Louis, Missouri, United States
Retina NorthwestPortland, Oregon, United States
Erie Retina ResearchErie, Pennsylvania, United States
Charles Retina InstituteGermantown, Tennessee, United States

+ 5 more locations — full list on the registry record.

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