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COMPLETED Phase 2

A Study Investigating the Efficacy and Safety of Intravitreal Injections of ANX007 in Patients With Geographic Atrophy

NCT04656561 · View on ClinicalTrials.gov ↗

Study Summary

This study is being conducted in participants with geographic atrophy (GA) secondary to age-related macular degeneration (AMD) to determine if intravitreal (IVT) injections of ANX007 reduce GA lesion growth rate. The results will be used to guide further development of ANX007 in participants with geographic atrophy. The total duration of participation is expected to be approximately 19 months.

Conditions Studied

Interventions

  • OTHER Sham comparator
  • DRUG ANX007

Study Locations (20)

California

  • Site 31 — Bakersfield
  • Site 2 — Beverly Hills
  • Site 19 — Mountain View
  • Site 23 — Pasadena
  • Site 37 — Poway
  • Site 17 — Sacramento
  • Site 18 — Santa Ana
  • Site 33 — Walnut Creek

Florida

  • Site 12 — Fort Myers
  • Site 53 — Jacksonville
  • Site 26 — Pensacola
  • Site 16 — Pinellas Park
  • Site 43 — Sarasota
  • Site 28 — St. Petersburg
  • Site 6 — Winter Haven

Arizona

  • Site 5 — Phoenix

Connecticut

  • Site 39 — Waterford

Georgia

  • Site 42 — Augusta

Kentucky

  • Site 11 — Lexington

Maryland

  • Site 1 — Hagerstown

Trial Details

FieldValue
Enrollment Target 270 participants
Start Date 2021-02-26
Est. Completion 2023-09-13
Phase Phase 2

Sponsor

Annexon

35 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04656561

The ClinicalTrials.gov registry entry for NCT04656561 describes a study currently listed as completed. It is categorized as Phase 2, 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 270 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Annexon, which has 35 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 2 interventions — of which Sham comparator 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: NCT04656561 reports 20 study locations spanning 7 distinct geographic areas — top geographies include California, Florida, Arizona. 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 NCT04656561 about?

NCT04656561 is a clinical study titled "A Study Investigating the Efficacy and Safety of Intravitreal Injections of ANX007 in Patients With Geographic Atrophy". This study is being conducted in participants with geographic atrophy (GA) secondary to age-related macular degeneration (AMD) to determine if intravitreal (IVT) injections of ANX007 reduce GA lesion growth rate. The results will be used to guide further development of ANX007 in participants with ge...

What is the current status of trial NCT04656561?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 270 participants. The study started on 2021-02-26. Estimated completion is 2023-09-13.

What conditions does trial NCT04656561 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 NCT04656561?

The interventions under investigation include: Sham comparator (OTHER), ANX007 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04656561?

This trial is sponsored by Annexon, which has 35 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04656561 being conducted?

This trial has 20 study locations across Arizona, California, Connecticut, Florida, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial