Brolucizumab 6 mg Drug Product Intended for Commercialization
A 24-Week, Double-Masked, Multicenter, Two-Arm Extension Study to Collect Safety and Efficacy Data on Brolucizumab 6 mg Drug Product Intended for Commercialization in Patients with Neovascular Age-Related Macular Degeneration who have Completed the Crth258a2301 Study
PI: William R. Freeman, M.D.
Efficacy of Zimura™ in Subjects with Geographic Atrophy (GA)
A Phase 2B Randomized, Double-Masked, Controlled Trial to Assess the Safety and Efficacy of Zimura™ (Anti-Complement Factor 5 Aptamer) in Subjects with Geographic Atrophy (GA) Secondary to Dry Age-Related Macular Degeneration
PI: William R. Freeman, M.D.
Intravitreal Opt-302 in Combination with Ranibizumab, Compared with Ranibizumab Alone
A Dose-Ranging Study of Intravitreal Opt-302 in Combination with Ranibizumab, Compared with Ranibizumab Alone, in Participants with Neovascular Age-Related Macular Degeneration (Wet AM.D.)
PI: Daniel L. Chao, M.D., Ph.D.
KESTREL
A Two-Year, Three-Arm, Randomized, Double-Masked, Multicenter, Phase III Study Assessing the Efficacy and Safety of Brolucizumab versus Aflibercept in Adult Patients with Visual Impairment due to Diabetic Macular Edema (KESTREL)
Nudleman Eric, M.D., Ph.D.
Lampalizumab Administered Intravitreally
A Phase III, Multicenter, Randomized, Double-Masked, Sham-Controlled Study to Assess the Efficacy and Safety of Lampalizumab Administered Intravitreally to Patients with Geographic Atrophy Secondary to Age-Related Macular Degeneration
PI: Henry Ferreyra M.D.
Lampalizumab in Patients with Geographic Atrophy Secondary
A Multicenter, Open-Label Extension Study to Evaluate the Long-Term Safety and Tolerability of Lampalizumab in Patients with Geographic Atrophy Secondary to Age-Related Macular Degeneration who have Completed a Roche-Sponsored Study
PI: Henry Ferreyra, M.D.
OAKS
A Phase 3, Multicenter, Randomized, Double-Masked, Sham-Controlled Study to Compare the Efficacy and Safety of Intravitreal APL-2 Therapy with Sham Injections in Patients with Geographic Atrophy 2nd to Age-Related Macular Degeneration (OAKS)
Chao Daniel L., M.D., Ph.D.
PANDA
A Multicenter, Double-Masked, Randomized, Dose-Ranging Trial to Evaluate the Efficacy and Safety of Conbercept Intravitreal Injection in Subjects with Neovascular Age-related Macular Degeneration (PANDA)
Chao Daniel L., M.D., Ph.D.
PORTAL
A Multicenter, Open-Label Extension Study to Evaluate the Long-Term Safety and Tolerability of the Port Delivery System with Ranibizumab in Patients with Neovascular Age-related Macular Degeneration (PORTAL)
Freeman William R., M.D.
RHINE
A Phase 3, Multicenter, Randomized, Double-Masked, Active Comparator-Controlled Study to Evaluate the Efficacy and Safety of RO6867461 in Patients with Diabetic Macular Edema (RHINE)
Chao Daniel L., M.D., Ph.D.
Rth258 Versus Aflibercept
A Two-Year, Randomized, Double-Masked, Multicenter, Three-Arm Study Comparing the Efficacy and Safety of Rth258 Versus Aflibercept in Subjects with Neovascular Age-Related Macular Degeneration
PI: William R. Freeman, M.D.
Sub-I: Eric Nudleman, M.D., Ph.D., Daniel L. Chao, M.D., Ph.D.
SAPPHIRE
Suprachoroidal Injection of Triamcinolone Acetonide with IVT Aflibercept in Subjects with Macular Edema Following Rvo (SAPPHIRE)
Chao Daniel L., M.D., Ph.D.
Suprachoroidal Cls-Ta
A Randomized, Masked, Controlled Trial to Study the Safety and Efficacy of Suprachoroidal Cls-Ta in Conjunction with Intravitreal Aflibercept in Subjects with Central Retinal Vein Occlusion
PI: Daniel L. Chao, M.D., Ph.D.
Sub-I: Eric Nudleman, M.D., Ph.D., William R. Freeman, M.D.
TENAYA
A Phase 3, Multicenter, Randomized, Double-Masked, Active Comparator-Controlled Study to Evaluate the Efficacy and Safety of FARICIMAB in Patients with Age-Related Macular Degeneration (TENAYA)