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NCT07230834RecruitingPhase 1

Intravitreal (IVT) Pozelimab for Geographic Atrophy (GA) in Adult Participants

A Phase 1 Dose-Escalation and Repeated-Dose Study of the Safety and Tolerability of Intravitreal Pozelimab in Participants With Geographic Atrophy

Source: ClinicalTrials.gov · Last updated 5 Aug 2026

Brief summary (registry, in English)

This study is researching an experimental drug called pozelimab (called "study drug"). The study is focused on people with a condition where certain parts of the eye's retina stop working over time, which can make it harder to see. This is called geographic atrophy (GA). The aim of the study is to see how safe and tolerable the study drug is when used as an injection in the eye. The study is looking at several other research questions, including: * What side effects may happen from taking the study drug * How much study drug is in the blood and the fluid in the eye at different times * Whether the body makes antibodies against the study drug (which could make the drug less effective or could lead to side effects)

Status (registry)
Recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
54 (estimated)
First submitted
13 Nov 2025
Start date
19 Jan 2026
Primary completion date
3 Jul 2028
Lead sponsor
Regeneron Pharmaceuticals
NCT number
NCT07230834
EU CT number
2025-521758-40-00

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 54
  • From 19 Jan 2026 to the primary completion date, 3 Jul 2028
  • 9 sites in 4 countries
  • 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

  • Concurrent eye disease (elevated Intraocular Pressure (IOP) \>25mm Hg, diabetic retinopathy, ocular infections/inflammation)
  • Prior or current intravitreal (IVT) treatment of any kind for any indication in either the study or fellow eye, except complement inhibitor therapy for GA, as long as last dose was ≥3 months prior to screening
  • Any prior systemic treatment for dry AMD, except oral supplements or vitamins
  • History or current use of systemic complement inhibitor therapy
    • Note: Other protocol-defined Inclusion/ Exclusion criteria apply

Other

  • GA (macular atrophy) in either eye due to causes other than dry AMD
  • History or current evidence of macular neovascularization and/or retinal exudation in either eye

Who the study is looking for

  • Study eye with diagnosis of GA of the macula secondary to AMD, as determined by the investigator
  • Study eye with total GA area measuring approximately one disc area or greater in size (2.5 mm\^2 or larger) at screening, as determined by the Central Reading Center (CRC), as described in the protocol
  • Best-Corrected Visual Acuity (BCVA) of 60 letters or worse using the Early Treatment Diabetic Retinopathy Score (ETDRS) charts (Snellen equivalent of \~ ≤20/63) in the study eye at screening and baseline visit

Age in the registry: 50 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (9)

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

SiteCityCountrySite status
Arensia Exploratory Medicine at the Research Institute of Clinical Medicine
Coordinator of this site? Confirm its status
TbilisiGeorgiaRecruiting
Emanuelli Research and Development Center
Coordinator of this site? Confirm its status
AreciboPuerto RicoRecruiting
Arensia Clinics S.R.L.
Coordinator of this site? Confirm its status
BucharestRomaniaRecruiting
Spitalul Clinic Judetean De Urgenta Cluj
Coordinator of this site? Confirm its status
Cluj-NapocaRomaniaRecruiting
Austin Retina Associates
Coordinator of this site? Confirm its status
AustinUnited StatesRecruiting
Retina Foundation of the Southwest
Coordinator of this site? Confirm its status
DallasUnited StatesRecruiting
Ophthalmic Consultants of Boston
Coordinator of this site? Confirm its status
East WeymouthUnited StatesRecruiting
Colorado Retina Associates
Coordinator of this site? Confirm its status
LakewoodUnited StatesRecruiting
Retina Consultants Texas
Coordinator of this site? Confirm its status
The WoodlandsUnited StatesRecruiting

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