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Completed Phase 1Phase 2 Interventional

Study of Zifibancimig in Participants With Neovascular Age-related Macular Degeneration

ClinicalTrials.gov ID: NCT04567303

Public ClinicalTrials.gov record NCT04567303. 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 27, 2026, 8:37 PM 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 Three-part, Phase I/II Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Efficacy of Zifibancimig Following Intravitreal Administration of Multiple Ascending Doses and Continuous Delivery From the Port Delivery in Patients With Neovascular Age-related Macular Degeneration

Brief summary

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

This is a first in-human study to investigate the safety, tolerability and efficacy of zifibancimig administered through intravitreal (IVT) injections and via the port delivery (PD) implant in participants with neovascular age-related macular degeneration (nAMD).

Study identification

NCT ID
NCT04567303
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
177 participants

Conditions and interventions

Interventions

Drug · Device

Eligibility (public fields only)

Age range
50 Years and older
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
Oct 28, 2020 (Actual)
Primary completion
Aug 25, 2026 (Actual)
Completion
Aug 25, 2026 (Actual)
Last update posted
Sep 14, 2026

2020 – 2026

United States locations

U.S. sites
36
U.S. states
22
U.S. cities
35
Facility City State ZIP Site status
Barnet Dulaney Perkins Eye Center Mesa Arizona 85206 —
Associated Retina Consultants Phoenix Arizona 85020 —
The Retina Partners Encino California 91436 —
Retinal Consultants Med Group Sacramento California 95841 —
Orange County Retina Med Group Santa Ana California 92705 —
Southwest Retina Consultants Durango Colorado 81303 —
Retina Vitreous Assoc of FL St. Petersburg Florida 33711 —
Southern Vitreoretinal Assoc Tallahassee Florida 32308 —
Southeast Retina Center Augusta Georgia 30909 —
University Retina and Macula Associates, PC Oak Forest Illinois 60452 —
Maine Eye Center Portland Maine 04101 —
Johns Hopkins Med Baltimore Maryland 21287 —
Retina Group of Washington Chevy Chase Maryland 20815 —
Cumberland Valley Retina Consultants Hagerstown Maryland 21740 —
Foundation for Vision Research Grand Rapids Michigan 49546 —
Associated Retinal Consultants Royal Oak Michigan 48073 —
VitreoRetinal Surgery, PLLC. Saint Louis Park Minnesota 55416 —
The Retina Institute St Louis Missouri 63128 —
Sierra Eye Associates Reno Nevada 89502 —
Envision Ocular, LLC Bloomfield New Jersey 07003 —
Retina Vit Surgeons/Central NY Liverpool New York 13088 —
Duke Eye Center Durham North Carolina 27705 —
Graystone Eye Hickory North Carolina 28602 —
OSU Eye Physicians & Surgeons Columbus Ohio 43212 —
Mid Atlantic Retina - Wills Eye Hospital Philadelphia Pennsylvania 19107 —
Carolina Eyecare Physicians Mt. Pleasant South Carolina 29464 —
Charles Retina Institute Germantown Tennessee 38138 —
Southeastern Retina Associates Knoxville Tennessee 37922 —
Tennessee Retina PC. Nashville Tennessee 37203 —
Austin Research Center for Retina Austin Texas 78705 —
Austin Clinical Research LLC Austin Texas 78750 —
Retina Consultants of Texas Bellaire Texas 77401 —
Retina Consultants of Texas Houston Texas 77030 —
Retina Center of Texas Southlake Texas 76092 —
Piedmont Eye Center Lynchburg Virginia 24502 —
Spokane Eye Clinical Research Spokane Washington 99204 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04567303, 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 14, 2026 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04567303 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →