Angioid Streaks
Conditions
Keywords
angioid streaks, CNV, intra vitreal ranibizumab
Brief summary
The purpose of this study is to determine whether injections of ranibizumab into the eye are safe and well tolerated when given to subjects in multiple doses.
Detailed description
Choroidal neovascularization is a hallmark of angioid streaks, and presumably VEGF-driven. Ranibizumab has been shown to be effective in CNV secondary to age-related macular degeneration. Therefore, we hypothesize that ranibizumab may be efficacious in the treatment of CNV secondary to angioid streaks
Interventions
DRUGranibizumab
0.5 mg dose of ranibizumab. Treatment will be given at baseline, month 1, and month 2, and then monthly until OCT shows absence of subretinal fluid and FA shows absence of leakage
Sponsors
Genentech, Inc.
University of Illinois at Chicago
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* Ability to provide written informed consent and comply with study assessments for the full duration of the study * Age \> 18 years * Angioid streaks * Subfoveal CNV of recent onset with the following characteristics * Absence of subfoveal fibrosis * Fibrosis less than 25% of the lesion * Presence of blood, subretinal fluid, and/or lipid * New onset symptoms within 12 weeks * Visual acuity 20/40 to 20/800 on an ETDRS chart
Exclusion criteria
* Prior treatment of subfoveal CNV in the study eye * Age-related macular degeneration * Uncontrolled glaucoma * High myopia (\> -10.00 D spherical equivalent) * Prior retinal detachment * Media opacity preventing adequate view of the retina * Planned cataract surgery in the next 3 months * Current chemotherapy for cancer * Immunocompromised state * Pregnancy (positive pregnancy test) or lactation * Premenopausal women not using adequate contraception. * Any other condition that the investigator believes would pose a significant hazard to the subject if the investigational therapy were initiated * Participation in another simultaneous medical investigation or trial * History of any previous treatment for angioid streaks
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome measures for safety and tolerability are the following: • Incidence and severity of ocular adverse events, as identified by eye examination (including visual acuity testing) | Month 12 |
Secondary
| Measure | Time frame |
|---|---|
| Proportion of patients that lose fewer than 15 letters from baseline at months 6 and 12 as assessed by the number of letters read correctly on the ETDRS eye chart at a starting test distance of 4 meters at months 6 and 12 | Month 6 and 12 |
Outcome results
None listed