Zimura in Participants With Geographic Atrophy Secondary to Dry Age-Related Macular Degeneration
Geographic Atrophy, Macular Degeneration
About this trial
This is an interventional treatment trial for Geographic Atrophy focused on measuring Geographic Atrophy (GA), Dry age-related macular degeneration, AMD, Zimura, Anti-inflammatory, complement factor C5 inhibitor, ARC1905, avacincaptad pegol
Eligibility Criteria
Inclusion Criteria:
- Subjects of either gender aged ≥ 50 years
- Diagnosis of Non-foveal GA secondary to dry AMD
Exclusion Criteria:
- Evidence of Choroidal Neovascularization (CNV)
- GA secondary to any condition other than AMD
- Any prior treatment for AMD or any prior intravitreal treatment for any indication in either eye, except oral supplements of vitamins and minerals
- Any intraocular surgery or thermal laser within three (3) months of trial entry
- Any prior thermal laser in the macular region, regardless of indication
- Any ocular or periocular infection in the twelve (12) weeks
- Previous therapeutic radiation in the region of the study eye
- Any sign of diabetic retinopathy in either eye
Sites / Locations
- Retina Consultants of Hawaii
- Clinical hospital center Osijek
- Fakultni Nemocnice Brno
- Faculty Hospital Hradec Kralove
- Fakultni nemocnice Olomouc
- Axon Clinical SRO
- East Tallinn Central Hospital
- Dr.Kai Noor Eye Clinic
- Peterfy Korhaz-Rendelointezet Orszagos Traumatologiai Intezet
- Rambam Medical Center
- Hadassah University Hospital
- Meir Medical Center
- Rabin Medical Center
- Kaplan Medical Center
- Tel-Aviv Sourasky Medical Center
- Pauls Stradins Clinical University Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Arm 6
Experimental
Experimental
Sham Comparator
Experimental
Experimental
Sham Comparator
Zimura 1 mg [Part 1]
Zimura 2 mg [Part 1]
Sham [Part 1]
Zimura 2 mg (Zimura 2mg+Sham) [Part 2]
Zimura 4 mg (Zimura 2mg+Zimura 2mg) [Part 2]
Sham (Sham+Sham) [Part 2]
Participants received 1 mg of Zimura in the study eye administered via IVT injection (50 µL) on Day 1 and monthly up to 18 months.
Participants received 2 mg of Zimura in the study eye administered via IVT injection (100 µL) on Day 1 and monthly up to 18 months.
Participants received a Sham injection of an empty, needleless syringe administered in the study eye on Day 1 and monthly up to 18 months.
Participants received 2 mg of Zimura in the study eye administered via IVT injection (100 µL) and a subsequent Sham administration on Day 1 and monthly up to 18 months.
Participants received 4 mg of Zimura in the study eye administered via two consecutive IVT injections (2 x 100 µL) on Day 1 and monthly up to 18 months.
Participants received two consecutive Sham injections of empty, needleless syringes administered in the study eye on Day 1 and monthly up to 18 months.