Intravitreal Aflibercept Injections In The Treatment Of Pattern Dystrophy
NCT01965041 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL
Last updated 2014-12-31
Summary
Adult-onset vitelliform detachments associated with pattern dystrophy is a genetic disorder that carries visual implications that most commonly affect the macula (area in the eye near the retina that is essential for sharp central vision). Adult onset vitelliform detachments have an accumulation of material on the outer retina. Over time, the abnormal accumulation of this material can damage cells that are critical for clear central vision. As a result, people with this disorder often lose their central vision, and their eyesight may become blurry or distorted.
Conditions
- Pattern Dystrophy of Macula
Interventions
- DRUG
-
2.0 mg intravitreal aflibercept injection is formulated as a sterile liquid to a final concentration of 40 mg/mL aflibercept in 5% sucrose, 10 mM sodium phosphate pH 6.3, 0.03% polysorbate 20, and 40 mM NaClvs. placebo
Sponsors & Collaborators
-
Northwell Health
collaborator OTHER -
Manhattan Eye, Ear & Throat Hospital
lead OTHER
Principal Investigators
-
Lawrence A. Yannuzzi, M.D. · Northshore Long Island Jewish Healthcare Systems
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 50 Years
- Max Age
- 90 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2013-10-31
- Primary Completion
- 2014-11-30
- Completion
- 2014-11-30
Countries
- United States
Study Locations
More Related Trials
-
A Study to Learn How Well Aflibercept Injected Into the Eye Works and How Safe it is When Given in Customized Treatment Intervals in Patients With an Eye Disease Called Neovascular Age-related Macular Degeneration After Start of Treatment
NCT05473715 ·Status: TERMINATED ·Phase: PHASE4
-
Aflibercept Injection Into the Vitreous Body of the Eye: Study to Learn More About Patient Relevant Outcomes, Real World Treatment Patterns and How Well the Treatment Works for Patients Suffering From Abnormal Growth of New Blood Vessels Under the Retina.
NCT03714308 ·Status: COMPLETED
-
Intense Treatment Regimen With Intravitreal Aflibercept Injection
NCT03594461 ·Status: UNKNOWN ·Phase: PHASE1/PHASE2
-
A Study to Learn How Well a Higher Amount of Aflibercept Given as an Injection Into the Eye Works and How Safe it is in People With Reduced Vision Due to Swelling in the Macula, Central Part of the Retina Caused by a Blocked Vein in the Retina (Macula Edema Secondary to Retinal Vein Occlusion)
NCT05850520 ·Status: COMPLETED ·Phase: PHASE3
-
Short-term Clinical Effects of Intravitreal Aflibercept Injection 2.0mg as a Predictor of Long-term Results
NCT01657669 ·Status: UNKNOWN ·Phase: PHASE4
-
Study of the Effects of High Dose Aflibercept Injected Into the Eye of Patients With an Age-related Disorder That Causes Loss of Vision Due to Growth of Abnormal Blood Vessels at the Back of the Eye
NCT04423718 ·Status: COMPLETED ·Phase: PHASE3
-
Study of the Efficacy and Safety of Intravitreal (IVT) Aflibercept for the Improvement of Moderately Severe to Severe Nonproliferative Diabetic Retinopathy (NPDR)
NCT02718326 ·Status: COMPLETED ·Phase: PHASE3
-
Intravitreal Aflibercept Injection for Symptomatic Macular Edema From Retinal Artery Macroaneurysms
NCT02403128 ·Status: UNKNOWN ·Phase: PHASE1
-
Evaluation of the Retina in Patients With Non-proliferative Diabetic Retinopathy After Aflibercept Injection in the Eye
NCT04702048 ·Status: WITHDRAWN ·Phase: PHASE4
-
EYE001 to Treat Retinal Tumors in Patients With Von Hippel-Lindau Syndrome
NCT00056199 ·Status: COMPLETED ·Phase: PHASE1
-
Intravitreal Aflibercept for Submacular Hemorrhage
NCT03169660 ·Status: COMPLETED ·Phase: PHASE4
-
Plasma Levels of Vascular Endothelial Growth Factor Before and After Intravitreal Injection of Aflibercept
NCT02125864 ·Status: COMPLETED ·Phase: PHASE4
-
SAD of IVT VP-001 in PRPF31 Mutation-Associated Retinal Dystrophy Subjects
NCT05902962 ·Status: COMPLETED ·Phase: PHASE1
-
A Study in Subjects With Retinal Detachment
NCT00210067 ·Status: COMPLETED ·Phase: PHASE1
-
Safety, Tolerability, and Efficacy of Aflibercept in Patients With Neovascular Age-Related Macular Degeneration
NCT04126317 ·Status: COMPLETED ·Phase: PHASE2
-
Aflibercept 8 mg for nAMD: Early Anatomical and Functional Changes
NCT07074054 ·Status: COMPLETED
-
Two-week Retreatment Interval Study for Treated Age-related Macular Degeneration Refractory to Monthly Aflibercept
NCT03468296 ·Status: UNKNOWN ·Phase: PHASE4
-
Repeated Eye Injections of Aflibercept for Treatment of Wet Age Related Macular Degeneration
NCT01773954 ·Status: COMPLETED ·Phase: NA
-
Effect Aflibercept on Ocular Perfusion
NCT03804099 ·Status: COMPLETED ·Phase: PHASE4
-
Study of MP0112 Intravitreal Injection in Patients With Wet Age Related Macular Degeneration
NCT01086761 ·Status: TERMINATED ·Phase: PHASE1
-
An Observational Study to Investigate the Use of Aflibercept 8 mg to Treat Adult Patients With Neovascular Age-Related Macular Degeneration (nAMD) and Diabetic Macular Edema (DME) in a Real-World Setting
NCT06398080 ·Status: WITHDRAWN
-
Maximum Treatment Interval With Aflibercept T&E
NCT05342857 ·Status: UNKNOWN
-
Study of Intravitreal Aflibercept Injection for Persistent CRVO-associated Macular Edema Despite Prior Anti-VEGF Therapy
NCT01857544 ·Status: UNKNOWN ·Phase: PHASE4
-
A Study Testing if Medicine Can Make Pigment Epithelium Detachments Regress and Stabilize the Vision in Eyes
NCT01746875 ·Status: TERMINATED ·Phase: NA
-
Prospective Observational Study to Assess Effectiveness of Intravitreal Aflibercept in Patients With Wet Macular Degeneration in Greece
NCT02821247 ·Status: COMPLETED