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NCT06779773Active, not recruiting

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

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

Source: ClinicalTrials.gov · Last updated 27 Oct 2026

Brief summary (registry, in English)

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.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
488 (actual)
First submitted
16 Dec 2024
Start date
22 Jan 2025
Primary completion date
31 Oct 2030
Lead sponsor
Astellas Pharma Global Development, Inc.
NCT number
NCT06779773

What you commit to

  • Study type: Observational
  • Participants enrolled: 488
  • From 22 Jan 2025 to the primary completion date, 31 Oct 2030
  • 57 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients who have any contraindication or are not eligible for treatment with ACP, including the following:
    • Active ocular or peri-ocular infection in either eye
    • Active, suspected intraocular inflammation in either eye
    • Hypersensitive to ACP or to any ingredient in the formulation
  • Patients who have received ACP in the eye being considered for enrollment. Note: Patients who have received or are receiving ACP in the fellow eye at baseline are eligible to be included in the study.
  • Patients who have received any intravitreal complement inhibitor other than ACP in either eye. Note: Patients who have received an intravitreal complement inhibitor other than ACP in either eye and have completed the 90-day washout period are eligible to be included in the study.

Other

  • Patients currently participating in an investigational program with interventions outside of routine clinical practice.

Who the study is looking for

  • Patients with geographic atrophy (GA) secondary to age-related macular degeneration (AMD) in 1 or both eyes
  • Patient with a decision to treat with intravitreal avacincaptad pegol (ACP) prior to enrollment
  • Patient willingness to complete the patient reported outcome (PRO).

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (57)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Retina Research Institute of Texas
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AbileneUnited StatesUnknown status
Southeast Retina Center, P.C.
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AugustaUnited StatesUnknown status
Rocky Mountain Lions Eye Institute
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AuroraUnited StatesUnknown status
Advanced Retina Institute
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Bonita SpringsUnited StatesUnknown status
SightMD
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BrentwoodUnited StatesUnknown status
Retina Consultants of Southern Colorado
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Colorado SpringsUnited StatesUnknown status
The Ohio State University
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ColumbusUnited StatesUnknown status
University of Miami
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Coral GablesUnited StatesUnknown status
Retina of North Texas
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DallasUnited StatesUnknown status
CEI Physicians PSC, LLC dba
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DaytonUnited StatesUnknown status
Eye Associates of North Jersey PA
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DoverUnited StatesUnknown status
NJ Retina
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EdisonUnited StatesUnknown status
Erie Retina Research
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ErieUnited StatesUnknown status
Verum Research, LLC
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EugeneUnited StatesUnknown status
The Retina Group of Washington
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FairfaxUnited StatesUnknown status
Retina Associates of Michigan
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Grand BlancUnited StatesUnknown status
Coastal Eye Surgeons
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GreenwichUnited StatesUnknown status
Cumberland Valley Retina Consultants,P.C.
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HagerstownUnited StatesUnknown status
Southeastern Retina Associates, P.C.
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KnoxvilleUnited StatesUnknown status
Harvard Eye Associates
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Laguna HillsUnited StatesUnknown status
NJ Retina
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LakewoodUnited StatesUnknown status
Colorado Retina Associates, PLLC
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LakewoodUnited StatesUnknown status
Retina-Vitreous Surgeons of Central NY
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LiverpoolUnited StatesUnknown status
Piedmont Eye Center, Inc.
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LynchburgUnited StatesUnknown status
Mississippi Retina Associates
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MadisonUnited StatesUnknown status
NY Retina Ophthalmology PLLC
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MassapequaUnited StatesUnknown status
Valley Retina Institute
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McAllenUnited StatesUnknown status
Mid South Retina Associates
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MemphisUnited StatesUnknown status
Retina & Vitreous Consultants of Wisconsin
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MilwaukeeUnited StatesUnknown status
Retina Associates of Utah, P.C.
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MurrayUnited StatesUnknown status
Tennessee Retina, PC
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NashvilleUnited StatesUnknown status
Retina Associates of New York
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New YorkUnited StatesUnknown status
University Retina and Macula Associates, P.C.
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Oak ForestUnited StatesUnknown status
Illinois Retina Associates
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Oak ParkUnited StatesUnknown status
Brown Family Retina PLLC
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Olive BranchUnited StatesUnknown status
University of California Irvine Medical Center
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OrangeUnited StatesUnknown status
Retina Care Specialists
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Palm Beach GardensUnited StatesUnknown status
Illinois Eye Center
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PeoriaUnited StatesUnknown status
Retinal Consultants of AZ
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PhoenixUnited StatesUnknown status
Retina Consultants of Southern CA
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RedlandsUnited StatesUnknown status
Sierra Eye Associates
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RenoUnited StatesUnknown status
Retinal Consultants Medical Group, Inc.
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SacramentoUnited StatesUnknown status
Retina Consultants of Minnesota PLLC
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Saint Louis ParkUnited StatesUnknown status
Salt Lake Retina
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Salt Lake CityUnited StatesUnknown status
Retina Associates of South Texas PA
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San AntonioUnited StatesUnknown status
Medical Center Ophthalmology Associates
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San AntonioUnited StatesUnknown status
Long Island Vitreoretinal Consultants
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ScarsdaleUnited StatesUnknown status
Retina Macula Institute of Arizona
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ScottsdaleUnited StatesUnknown status
Vitreoretinal Consultants
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ShirleyUnited StatesUnknown status
Deep Blue Retina Clinical Research
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SouthavenUnited StatesUnknown status
Eye Physicians of Pinellas PA dba Eye Institute of West Florida
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TampaUnited StatesUnknown status
NJ Retina
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Toms RiverUnited StatesUnknown status
Retina Macula Institute
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TorranceUnited StatesUnknown status
North Carolina Retina Associates
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Wake ForestUnited StatesUnknown status
Virginia Retina Center
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WarrentonUnited StatesUnknown status
Retina Specialists of Tampa
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Wesley ChapelUnited StatesUnknown status
Wolfe Eye Clinic
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West Des MoinesUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.