Last updated on June 2019

A Study Assessing the Safety Tolerability and Efficacy of RO7171009 in Participants With Geographic Atrophy Secondary to Age-Related Macular Degeneration (AMD)


Brief description of study

This study will evaluate the safety, tolerability, and efficacy of intravitreal injections of RO7171009 administered every 4 weeks (Q4W) or every 8 weeks (Q8W) for approximately 76 weeks in participants with geographic atrophy (GA) secondary to age-related macular degeneration (AMD) compared with sham control.

Clinical Study Identifier: NCT03972709

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Reno, NV United States
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Bloomfield, NJ United States
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Teaneck, NJ United States
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Toms River, NJ United States
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Hauppauge, NY United States
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Rockville Centre, NY United States
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Slingerlands, NY United States
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Winston-Salem, NC United States
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Cincinnati, OH United States
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Cleveland, OH United States
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Recruitment Status: Open


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