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A Prospective, Multicenter, Open-Label, Observational Phase 4 Study to Evaluate Real-World Safety, Tolerability, and Treatment Patterns of Pegcetacoplan (Syfovre) in Patients With Geographic Atrophy Secondary to Age-Related Macular Degeneration
NCT06161584 · View on ClinicalTrials.gov ↗
Study Summary
A Prospective, Multicenter, Open-Label, Observational Phase 4 Study to Evaluate Real-World Safety, Tolerability, and Treatment Patterns of Pegcetacoplan (Syfovre) in Patients with Geographic Atrophy Secondary to Age-Related Macular Degeneration
Conditions Studied
Interventions
- DRUG Pegcetacoplan
Study Locations (20)
California
- California Retina Consultants (01-026) — Bakersfield
- Retina-Vitreous Associates Medical Group (01-020) — Beverly Hills
- Illinois Retina Associates (01-035) — Fullerton
- Retinal Consultants Medical Group Inc (01-008) — Modesto
- Retina Consultants San Diego Inc. (01-018) — Poway
- California Retina Consultants (01-027) — Santa Barbara
- Bay Area Retina Associates (01-005) — Walnut Creek
Maryland
- The Retina Care Center (01-023) — Baltimore
- Cumberland Valley Retina Consultants, P.C. (01-002) — Hagerstown
- Mid Atlantic Retina Specialist (01-029) — Hagerstown
Georgia
- South East Retina Center, PC (01-030) — Augusta
- Georgia Retina (01-032) — Marietta
New Jersey
- Mid Atlantic Retina Research (01-014) — Cherry Hill
- Mid Atlantic Retina (01-031) — Cherry Hill
New York
- OCLI Research Department (01-007) — Oceanside
- Long Island Vitreoretinal Consultants (01-013) — Westbury
Colorado
- Colorado Retina Associates, PLLC (01-011) — Lakewood
Florida
- Retina Specialty Institute (01-019) — Pensacola
Illinois
- Illinois Retina Associates (01-037) — Oak Park
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 300 participants |
| Start Date | 2023-09-28 |
| Est. Completion | 2027-06 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06161584
The ClinicalTrials.gov registry entry for NCT06161584 describes a study currently listed as active not recruiting. It is categorized as an unspecified phase, 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 300 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Apellis Pharmaceuticals, which has 9 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 Geographic Atrophy appearing as the primary indexed condition, and to 1 intervention — of which Pegcetacoplan 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: NCT06161584 reports 20 study locations spanning 9 distinct geographic areas — top geographies include California, Maryland, Georgia. 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 NCT06161584 about?
NCT06161584 is a clinical study titled "A Prospective, Multicenter, Open-Label, Observational Phase 4 Study to Evaluate Real-World Safety, Tolerability, and Treatment Patterns of Pegcetacoplan (Syfovre) in Patients With Geographic Atrophy Secondary to Age-Related Macular Degeneration". A Prospective, Multicenter, Open-Label, Observational Phase 4 Study to Evaluate Real-World Safety, Tolerability, and Treatment Patterns of Pegcetacoplan (Syfovre) in Patients with Geographic Atrophy Secondary to Age-Related Macular Degeneration
What is the current status of trial NCT06161584?
This trial is currently active not recruiting. The enrollment target is 300 participants. The study started on 2023-09-28. Estimated completion is 2027-06.
What conditions does trial NCT06161584 study?
This clinical trial studies the following conditions: Geographic Atrophy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06161584?
The interventions under investigation include: Pegcetacoplan (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06161584?
This trial is sponsored by Apellis Pharmaceuticals, which has 9 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06161584 being conducted?
This trial has 20 study locations across California, Colorado, Florida, Georgia, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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