Recruiting

Avacincaptad Pegol in Geographic Atrophy from Age-related Macular Degeneration

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What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Eye Diseases+2

+ Macular Degeneration

+ Retinal Degeneration

+7 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: January 2025
See protocol details

Summary

Principal SponsorAstellas Pharma Global Development, Inc.
Study ContactAstellas Pharma Global Development, Inc.
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: January 22, 2025

Actual date on which the first participant was enrolled.

This study focuses on individuals with a condition called geographic atrophy, which is a severe form of age-related macular degeneration (AMD). AMD affects the macula, the part of the retina responsible for clear central vision, leading to vision deterioration. Geographic atrophy involves the gradual loss of cells in the retina, potentially resulting in permanent vision loss. The study aims to better understand how avacincaptad pegol, a treatment approved in the U.S. to slow the progression of this condition, is used in real-world clinical settings. By gathering information on treatment patterns and any medical issues related to avacincaptad pegol, researchers hope to improve care for individuals with this challenging eye condition. Participants in the study will receive their usual eye examinations as part of routine care, and their doctors will prescribe avacincaptad pegol if they deem it appropriate. This is an observational study, meaning it collects data without influencing treatment decisions. Information about the frequency and dosage of avacincaptad pegol injections, as well as the duration and reasons for stopping treatment, will be gathered from medical records. Participants will also complete surveys about their eye health when they start the treatment and periodically for up to five years. These surveys will help track any changes in their condition and the impact of the treatment over time.

Official TitleA 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
NCT06779773
Principal SponsorAstellas Pharma Global Development, Inc.
Study ContactAstellas Pharma Global Development, Inc.
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

1000 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Eye DiseasesMacular DegenerationRetinal DegenerationRetinal DiseasesGeographic Atrophy

Criteria

3 inclusion criteria required to participate
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).

4 exclusion criteria prevent from participating
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 at enrollment/baseline visit, Hypersensitive to ACP or to any ingredient in the formulation

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

Patients who have received ACP in the study eye. Note: Patients who have received or are receiving ACP in the fellow eye 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.

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 60 locations

Recruiting

Phoenix Retina Clinical Trials, LLC

Phoenix, United StatesOpen Phoenix Retina Clinical Trials, LLC in Google Maps
Recruiting

Retinal Consultants of AZ

Phoenix, United States
Recruiting

Retina Macula Institute of Arizona

Scottsdale, United States
Recruiting

The Retina Partners

Encino, United States
Recruiting
60 Study Centers