ADVM-022 (AAV.7m8-aflibercept) is a gene therapy product developed for the treatment of neovascular (wet) age-related macular degeneration (wet AMD). Wet AMD is a serious condition and the leading cause of blindness in the elderly. The available therapies for treating wet AMD require life-long intravitreal (IVT) injections every 4-12 weeks to maintain efficacy. A one-time IVT administration of ADVM-022 has the potential to treat wet AMD by providing durable expression of therapeutic levels of intraocular anti-VEGF protein (aflibercept) and maintaining the vision of patients. ADVM-022 is designed to reduce the current treatment burden which often results in undertreatment and vision loss in patients with wet AMD receiving anti-VEGF therapy in clinical practice.
This open-label, multicenter, dose-ranging study will evaluate 2 dose levels in up to 30 subjects (15 per dose) with active choroidal neovascularization (CNV) secondary to AMD. Subjects who are under active anti-VEGF treatment and have demonstrated a meaningful response to anti-VEGF therapy will be considered for participation in this study. The primary endpoint for this study is safety and tolerability of ADVM-022. All subjects will continue to be assessed for 104 weeks following treatment with ADVM-022.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
30
ADVM-022 (AAV.7m8-aflibercept) is a recombinant, replication-deficient adeno-associated virus (AAV.7m8) gene therapy vector carrying a coding sequence for aflibercept
Adverum Clinical Site
Bakersfield, California, United States
Adverum Clinical Site
Beverly Hills, California, United States
Adverum Clinical Site
Golden, Colorado, United States
Adverum Clinical Site
Deerfield Beach, Florida, United States
Adverum Clinical Site
Reno, Nevada, United States
Adverum Clinical Site
Philadelphia, Pennsylvania, United States
Adverum Clinical Site
West Columbia, South Carolina, United States
Adverum Clinical Site
Nashville, Tennessee, United States
Adverum Clinical Site
Abilene, Texas, United States
Adverum Clinical Site
Houston, Texas, United States
...and 1 more locations
Type, severity, and incidence of ocular and systemic adverse events (AEs)
Type, severity, and incidence of ocular and systemic adverse events (AEs)
Time frame: 104 weeks
Change in best corrected visual acuity (BCVA)
Change in best corrected visual acuity (BCVA)
Time frame: 104 weeks
Change in central subfield thickness (CST) and macular volume measured by SD-OCT
Change in central subfield thickness (CST) and macular volume measured by SD-OCT
Time frame: 104 weeks
Percentage of subjects requiring anti-VEGF injections over time
Percentage of subjects requiring anti-VEGF injections over time
Time frame: 104 weeks
Mean number of anti-VEGF injections over time
Mean number of anti-VEGF injections over time
Time frame: 104 weeks
Percentage of subjects without intraretinal fluid over time
Percentage of subjects without intraretinal fluid over time
Time frame: 104 weeks
Percentage of subjects without subretinal fluid over time
Percentage of subjects without subretinal fluid over time
Time frame: 104 weeks
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