This Phase 1, open-label, multicenter study will investigate the safety and tolerability of RO7171009 following single and multiple intravitreal (ITV) administrations in patients with GA secondary to AMD. The study consists of two stages: Single Dose-Escalation (SAD) and Multiple-Dose (MD) stages.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
28
Patients will receive RO7171009 via ITV injection.
California Retina Consultants
Bakersfield, California, United States
Northern California Retina Vitreous Associates
Mountain View, California, United States
Retinal Consultants Med Group
Sacramento, California, United States
Safety and Tolerability of the Study Drug: Rate of Adverse Events
Time frame: Through study completion or early study discontinuation (overall 12-20 weeks)
Serum Concentration of RO7171009
Time frame: Through study completion or early study discontinuation (overall 12-20 weeks)
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California Retina Consultants
Santa Barbara, California, United States
California Retina Consultants - Santa Maria
Santa Maria, California, United States
Retina Consultants of Southern Colorado PC; Clinical Research Department
Colorado Springs, Colorado, United States
Florida Eye Associates
Melbourne, Florida, United States
Retina Specialty Institute
Pensacola, Florida, United States
Georgia Retina PC
Marietta, Georgia, United States
The Retina Institute
St Louis, Missouri, United States
...and 3 more locations