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4D-150 in Patients With Macular Neovascularization Secondary to Age-Related Macular Degeneration
NCT06864988 · View on ClinicalTrials.gov ↗
Study Summary
A Phase 3, Randomized, Double-Masked, Active-Controlled Trial in Adults with Macular Neovascularization Secondary to Age-Related Macular Degeneration
Conditions Studied
Interventions
- BIOLOGICAL 4D-150 IVT (3E10 vg/eye)
- BIOLOGICAL EYLEA® (aflibercept) Injection 2 mg (0.05mL)
Study Locations (20)
California
- California Retina Consultants — Bakersfield
- Retina Vitreous Associates Medical Group — Beverly Hills
- The Retina Partners — Encino
- Retina Associates of Southern California — Huntington Beach
- Loma Linda University Faculty Medical Clinics — Loma Linda
- Jules Stein Eye Institute — Los Angeles
- Northern California Retina Vitreous Associates — Mountain View
- Gavin Herbert Eye Institute — Orange
- Retina Consultants of San Diego — Poway
- Kaiser Permanente-Riverside Medical Center — Riverside
- Retinal Consultants Medical Group Inc — Sacramento
- Retinal Consultants Medical Group Inc — Sacramento
- Orange County Retina Medical Group — Santa Ana
- California Retina Consultants - Santa Barbara — Santa Barbara
- Bay Area Retina Associates — Walnut Creek
Arizona
- Barnet Dulaney Perkins Eye Center — Phoenix
- Retinal Research Institute, LLC — Scottsdale
Colorado
- University of Colorado, Denver — Aurora
- Retina Consultants of Southern Colorado — Colorado Springs
Arkansas
- Retina Partners of Northwest Arkansas — Springdale
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 480 participants |
| Start Date | 2025-03-03 |
| Est. Completion | 2028-06 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06864988
The ClinicalTrials.gov registry entry for NCT06864988 describes a study currently listed as recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 480 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is 4D Molecular Therapeutics, which has 36 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Macular Neovascularization Secondary to Age-Related Macular Degeneration appearing as the primary indexed condition, and to 2 interventions — of which 4D-150 IVT (3E10 vg/eye) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06864988 reports 20 study locations spanning 4 distinct geographic areas — top geographies include California, Arizona, Colorado. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06864988 about?
NCT06864988 is a clinical study titled "4D-150 in Patients With Macular Neovascularization Secondary to Age-Related Macular Degeneration". A Phase 3, Randomized, Double-Masked, Active-Controlled Trial in Adults with Macular Neovascularization Secondary to Age-Related Macular Degeneration
What is the current status of trial NCT06864988?
This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 480 participants. The study started on 2025-03-03. Estimated completion is 2028-06.
What conditions does trial NCT06864988 study?
This clinical trial studies the following conditions: Macular Neovascularization Secondary to Age-Related Macular Degeneration. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06864988?
The interventions under investigation include: 4D-150 IVT (3E10 vg/eye) (BIOLOGICAL), EYLEA® (aflibercept) Injection 2 mg (0.05mL) (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06864988?
This trial is sponsored by 4D Molecular Therapeutics, which has 36 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06864988 being conducted?
This trial has 20 study locations across Arizona, Arkansas, California, Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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