A Study Using Intravitreal Injections of a Small Interfering RNA in Patients With Age-Related Macular Degeneration
NCT00395057 · Status: TERMINATED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 138
Last updated 2015-09-07
Summary
This is a 24-month study to evaluate multiple doses of AGN211745 (previously known as Sirna-027) in treatment of subfoveal choroidal neovascularization associated with age-related macular degeneration
Conditions
- Choroid Neovascularization
- Age-Related Macular Degeneration
Interventions
- DRUG
-
AGN 211745
AGN 211745 Solution 1000µg injection at Day 1, Month 1, Month 2
- DRUG
-
AGN 211745
AGN 211745 Solution 300µg injections, Day 1, Month 1, Month 2
- DRUG
-
AGN 211745
AGN 211745 Solution 100µg injections, Day 1, Month 1, Month 2
- DRUG
-
Ranibizumab 500µg
Ranibizumab 500µg injections at Day 1, Month 1, Month 2
Sponsors & Collaborators
-
Allergan
lead INDUSTRY
Principal Investigators
-
Medical Director · Allergan
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 50 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2007-01-31
- Primary Completion
- 2008-10-31
- Completion
- 2009-02-28
Countries
- United States
- Australia
- Philippines
Study Locations
More Related Trials
-
Efficacy and Safety of Two Treatment Regimens of 0.5 mg Ranibizumab Intravitreal Injections Guided by Functional and/or Anatomical Criteria, in Patients With Neovascular Age-related Macular Degeneration
NCT01780935 ·Status: COMPLETED ·Phase: PHASE3
-
Intravitreal Aflibercept in Neovascular AMD With Limited Response to Ranibizumab
NCT02309281 ·Status: COMPLETED ·Phase: PHASE4
-
Ranibizumab for Treating Submacular Vascularized Pigment Epithelial Detachments
NCT00749021 ·Status: COMPLETED ·Phase: PHASE1
-
Comparison of Treatment Regimens Using Ranibizumab: Intensive (Resolution of Intra- and Sub-retinal Fluid) vs Relaxed (Resolution of Intra-retinal Fluid and/or Sub-retinal Fluid >200µm at the Foveal Centre)
NCT01972789 ·Status: COMPLETED ·Phase: PHASE4
-
Study To Determine Safety/Efficacy of Lucentis For Treatment Of Retinal Angiomatous Proliferation Secondary To Age Related Macular Degeneration
NCT00395707 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Prophylactic Ranibizumab for Exudative Age-related Macular Degeneration
NCT02140151 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Study of the Efficacy and Safety of the Ranibizumab Port Delivery System for Sustained Delivery of Ranibizumab in Patients With Subfoveal Neovascular Age-Related Macular Degeneration
NCT02510794 ·Status: COMPLETED ·Phase: PHASE2
-
Study for Recalcitrant Age Related Macular Degeneration
NCT01543568 ·Status: COMPLETED ·Phase: PHASE4
-
A Study of rhuFab V2 (Ranibizumab) in Subjects With Subfoveal Choroidal Neovascularization Secondary to Age-Related Macular Degeneration (AMD)
NCT00090623 ·Status: COMPLETED ·Phase: PHASE3
-
A Proof-of-Concept Study of Faricimab (RO6867461) in Participants With Choroidal Neovascularization (CNV) Secondary to Age-Related Macular Degeneration (AMD)
NCT02484690 ·Status: COMPLETED ·Phase: PHASE2
-
A Phase III Study to Evaluate the Port Delivery System With Ranibizumab Compared With Monthly Ranibizumab Injections in Participants With Wet Age-Related Macular Degeneration
NCT03677934 ·Status: COMPLETED ·Phase: PHASE3
-
Ranibizumab Therapy for Choroidal Neovascularization (CNV) Asociated With Angioid Streaks
NCT01015495 ·Status: WITHDRAWN ·Phase: PHASE1/PHASE2
-
Intravitreal Ranibizumab in Exudative Age-related Macular Degeneration With Posterior Vitreomacular Adhesion
NCT01291121 ·Status: COMPLETED ·Phase: NA
-
A Clinical Effectiveness Study Examining the Efficacy and Safety of ONS-5010 in Subjects With Neovascular Age-related Macular Degeneration (AMD)
NCT03844074 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Evaluate rhuFab V2 in Subjects With Minimally Classic or Occult Subfoveal Neovascular Macular Degeneration
NCT00056836 ·Status: COMPLETED ·Phase: PHASE3
-
A Study of Ranibizumab Administered Monthly or on an As-needed Basis in Patients With Subfoveal Neovascular Age-related Macular Degeneration (HARBOR)
NCT00891735 ·Status: COMPLETED ·Phase: PHASE3
-
Assess the Efficacy/Safety of Intravitreal Ranibizumab in Patients With Vision Loss Due to Choroidal Neovascularization.
NCT01840410 ·Status: COMPLETED ·Phase: PHASE3
-
LHA510 Proof-of-Concept Study as a Maintenance Therapy for Patients With Wet Age-Related Macular Degeneration
NCT02355028 ·Status: COMPLETED ·Phase: PHASE2
-
A Clinical Effectiveness Study Examining the Efficacy and Safety of ONS-5010 in Subjects With Neovascular Age-related Macular Degeneration (AMD)
NCT03834753 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy and Safety of Ranibizumab in Patients With Visual Impairment Due to Choroidal Neovascularization Secondary to Pathologic Myopia
NCT01217944 ·Status: COMPLETED ·Phase: PHASE3
-
Intraocular Cytokines in Non-responders to Ranibizumab Treatment for Neovascular AMD
NCT02218177 ·Status: COMPLETED
-
Ranibizumab and Reduced Fluence PDT for AMD
NCT00527475 ·Status: COMPLETED ·Phase: PHASE2
-
Enhancing the Lucentis (Ranibizumab) Management of Choroidal Neovascular Membranes With Hyperspectral Imaging
NCT03105609 ·Status: TERMINATED
-
EXTEND III - Efficacy and Safety of Ranibizumab in Patients With Subfoveal Choroidal Neovascularization (CNV) Secondary to Age-related Macular Degeneration (AMD)
NCT00470678 ·Status: COMPLETED ·Phase: PHASE3
-
An Extension Study to Evaluate the Safety and Tolerability of Ranibizumab in Subjects With Choroidal Neovascularization Secondary to AMD or Macular Edema Secondary to RVO
NCT00379795 ·Status: COMPLETED ·Phase: NA