Macular neovascularization secondary to age-related macular degeneration (nAMD)
Conditions
Interventions
4D-150 IVT (3E10 vg/eye)
- Will be administered as a single dose IVT injection on Day 1
Aflibercept (EYLEA) Injection 2 mg (0.05mL) IVT
- Will be administered as IVT injection at applicable visits
Sponsors
Matsuda Rena
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: - >=50 years of age at time of consent - MNV secondary to nAMD with IVT anti-VEGF treatment history in the study eye, defined as EITHER: 1. Treatment naive, i.e. no prior IVT anti-VEGF therapy OR 2. Previously treated with no more than 4 IVT anti-VEGF injections due to nAMD and received diagnosis of nAMD no more than 6 months prior to the Screening Visit AND documented evidence of anatomical improvement and visual stability/improvement in response to previous IVT anti-VEGF treatment, as determined by the Investigator - Active subfoveal MNV or juxtafoveal/ extrafoveal MNV with a subfoveal component (where activity is defined as evidence of SRF, IRF, subretinal hyperreflective material, or leakage) identified by fluorescein angiography (FA) or spectral domain optical coherence tomography (SD-OCT), in the study eye, at the Screening Visit confirmed by the Reading Center - Demonstrated clinical response to aflibercept and functional stability in the study eye as confirmed by the Reading Center - BCVA between 25 and 78 ETDRS letters, inclusive (20/320-20/32 Snellen equivalent) in the study eye at the Screening Visit - CST less than or equal to 500 microns in the study eye at screening visit, confirmed by the central reading center
Exclusion criteria
Exclusion criteria: Ocular Conditions: - MNV due to causes other than nAMD in either eye (Fibrosis, atrophy, or subretinal hemorrhage in the foveal central subfield (1 mm diameter) - History of retinal detachment in the study eye - History of or presence of active inflammation in either eye - Glaucoma or intraocular hypertension requiring more than 2 topical medications for control Ocular Treatments/Interventions: - Any prior or concomitant treatment for MNV or vitreomacular-interface abnormalities, other than allowed prior IVT anti-VEGF in the study eye Systemic Conditions and Considerations: - Major illness or major surgical procedure in the 28 days prior to the Screening Visit - Uncontrolled blood pressure - Acute coronary syndrome, myocardial infarction or coronary artery revascularization, cerebrovascular accident, transient ischemic attack within 6 months of the Screening Visit - History of autoimmune condition that may predispose to the development of uveitis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Mean change from baseline in BCVA ETDRS letter score at Week 52 | — |
Secondary
| Measure | Time frame |
|---|---|
| - Mean annualized number of aflibercept injections after Week 4 through Weeks 52 and 104 - Incidence and timing of aflibercept injections after Week 4 through Weeks 52 and 104 - Proportion of subjects not requiring aflibercept injections after Week 4 through Weeks 52 and 104 in the 4D-150 arm - Mean change from baseline in CST over time through Weeks 52 and 104 - Mean change from baseline in BCVA ETDRS letter score over time through Weeks 52 and 104 | — |
Countries
Argentina, Australia, Brazil, Bulgaria, Colombia, Czech Republic, France, Germany, Hungary, Israel, Italy, Japan, Latvia, Lithuania, Poland, Portugal, Singapore, Slovakia, South Korea, Spain, United Kingdom, United States
Contacts
Public ContactRena Matsuda
Syneos Health Japan K.K.
Outcome results
None listed