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Active, not recruiting No phase listed Observational

A Study to Learn How Avacincaptad Pegol (Izervay™) is Used in Clinical Practice in People Who Have Geographic Atrophy

ClinicalTrials.gov ID: NCT06779773

Public ClinicalTrials.gov record NCT06779773. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 17, 2026, 9:00 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Non-interventional, Observational Study to Evaluate Treatment Patterns and Safety of Avacincaptad Pegol (ACP/IZERVAY™) in Routine Clinical Practice in Patients With Geographic Atrophy Secondary to Age-related Macular Degeneration

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study is for people who have geographic atrophy due to age-related macular degeneration (AMD). AMD happens when the macula, the light-sensitive layer at the back of the eye called the retina, becomes damaged and causes a person's central vision to worsen. Geographic atrophy is an advanced form of AMD where cells in the retina waste away and die. Over time this can lead to permanent loss of vision. Avacincaptad pegol can help slow down the worsening or progression of geographic atrophy. Avacincaptad pegol is a treatment approved in the US to treat geographic atrophy. This study is about collecting information on how people with geographic atrophy are treated in routine clinical practice. This includes recording any medical problems from avacincaptad pegol. This is known as an observational study. Information will be collected from the peoples' medical records during and after treatment. The people in this study will have geographic atrophy in 1 or both eyes and they and their doctor have decided they will be treated with avacincaptad pegol. The individual's doctor decides on treatment, not the study sponsor (Astellas). People that want to take part in the study will have eye examinations that they would usually have as part of their routine care. People will also be asked to complete surveys about their eye health. These surveys will occur when treatment starts and then every 6 months for the first 2 years. After 2 years the surveys will happen once a year. The people on the study can take part if their doctor provides treatment with avacincaptad pegol and they want to continue with the study. The people on the study can take part for around 5 years.

Study identification

NCT ID
NCT06779773
Recruitment status
Active, not recruiting
Study type
Observational
Phase
Not listed
Enrollment
489 participants

Conditions and interventions

Eligibility (public fields only)

Age range
Not listed
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 22, 2025 (Actual)
Primary completion
Oct 31, 2030 (Estimated)
Completion
Oct 31, 2030 (Estimated)
Last update posted
Sep 22, 2026

2025 – 2030

United States locations

U.S. sites
58
U.S. states
24
U.S. cities
56
Facility City State ZIP Site status
Retinal Consultants of AZ Phoenix Arizona 85053 —
Retina Macula Institute of Arizona Scottsdale Arizona 85255 —
Harvard Eye Associates Laguna Hills California 92653 —
University of California Irvine Medical Center Orange California 92868 —
Retina Consultants of Southern CA Redlands California 92374 —
Retinal Consultants Medical Group Inc Sacramento California 95825 —
Retina Macula Institute Torrance California 90503 —
Rocky Mountain Lions Eye Institute Aurora Colorado 80045 —
Retina Consultants of Southern Colorado Colorado Springs Colorado 80909 —
Colorado Retina Associates, PLLC Lakewood Colorado 80228 —
Coastal Eye Surgeons Greenwich Connecticut 05830 —
Advanced Retina Institute Bonita Springs Florida 34134 —
University of Miami Coral Gables Florida 33146 —
Retina Care Specialists Palm Beach Gardens Florida 33410 —
Eye Physicians of Pinellas PA dba Eye Institute of West Florida Tampa Florida 33606 —
Retina Specialists of Tampa Wesley Chapel Florida 33544 —
Southeast Retina Center, P.C. Augusta Georgia 30909 —
University Retina and Macula Associates, P.C. Oak Forest Illinois 60452 —
Illinois Retina Associates Oak Park Illinois 60304 —
Illinois Eye Center Peoria Illinois 61615 —
Wolfe Eye Clinic West Des Moines Iowa 50266 —
Cumberland Valley Retina Consultants,P.C. Hagerstown Maryland 21740 —
Retina Associates of Michigan Grand Blanc Michigan 48439 —
Retina Consultants of Minnesota PLLC Saint Louis Park Minnesota 55416 —
Mississippi Retina Associates Madison Mississippi 39110 —
Brown Family Retina PLLC Olive Branch Mississippi 38654 —
Deep Blue Retina Clinical Research Southaven Mississippi 38671 —
Sierra Eye Associates Reno Nevada 89502 —
Eye Associates of North Jersey PA Dover New Jersey 07801 —
NJ Retina Edison New Jersey 08820 —
NJ Retina Lakewood New Jersey 08701 —
NJ Retina Toms River New Jersey 08755 —
SightMD Brentwood New York 11717 —
Retina-Vitreous Surgeons of Central NY Liverpool New York 13088 —
NY Retina Ophthalmology PLLC Massapequa New York 11758 —
Retina Associates of New York New York New York 10075 —
Long Island Vitreoretinal Consultants Scarsdale New York 10583 —
Vitreoretinal Consultants Shirley New York 11967 —
North Carolina Retina Associates Wake Forest North Carolina 27587 —
The Ohio State University Columbus Ohio 43221 —
CEI Physicians PSC, LLC dba Dayton Ohio 45459 —
Verum Research, LLC Eugene Oregon 97401 —
Erie Retina Research Erie Pennsylvania 16507 —
Southeastern Retina Associates, P.C. Knoxville Tennessee 37920 —
Southeastern Retina Associates, P.C. Knoxville Tennessee 37923 —
Mid South Retina Associates Memphis Tennessee 38119 —
Tennessee Retina, PC Nashville Tennessee 37203 —
Retina Research Institute of Texas Abilene Texas 79606 —
Retina of North Texas Dallas Texas 75243 —
Valley Retina Institute McAllen Texas 78503 —
Medical Center Ophthalmology Associates San Antonio Texas 78240 —
Retina Associates Of South Texas, Pa San Antonio Texas 78240 —
Retina Associates of Utah, P.C. Murray Utah 84107 —
Salt Lake Retina Salt Lake City Utah 84120 —
The Retina Group of Washington Fairfax Virginia 22031 —
Piedmont Eye Center, Inc. Lynchburg Virginia 24502 —
Virginia Retina Center Warrenton Virginia 20186 —
Retina & Vitreous Consultants of Wisconsin Milwaukee Wisconsin 53226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06779773, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 22, 2026 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06779773 live on ClinicalTrials.gov.

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