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Active, not recruiting Phase 2 Interventional

A Study to Test Whether BI 771716 Helps People With an Advanced Form of Age-related Macular Degeneration (AMD) Called Geographic Atrophy

ClinicalTrials.gov ID: NCT06722157

Public ClinicalTrials.gov record NCT06722157. 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 18, 2026, 5:09 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

Randomized, Double-masked, Active-controlled, Multicenter Study to Evaluate Efficacy and Safety of Two Regimens of Intravitreal BI 771716 Against Pegcetacoplan in Participants With Geographic Atrophy Secondary to Age-related Macular Degeneration VERDANT Trial

Brief summary

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

This study is open to people 50 years or older with an eye condition called geographic atrophy. The purpose of this study is to compare a medicine called BI 771716 with a medicine called pegcetacoplan. BI 771716 is being developed to treat people with geographic atrophy. Pegcetacoplan is a medicine already used to treat people with geographic atrophy. In this study, participants receive either BI 771716 or pegcetacoplan as injections in the eye. Participants are in the study for a little longer than a year and visit the study site every 4 weeks. At the visits, the study doctor checks the eyes of the participants. The results are compared between the groups of participants to see whether the treatment works. The study doctor also regularly checks participants' health and takes note of any unwanted effects.

Study identification

NCT ID
NCT06722157
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
202 participants

Conditions and interventions

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
Jan 6, 2025 (Actual)
Primary completion
Oct 28, 2026 (Estimated)
Completion
Oct 28, 2026 (Estimated)
Last update posted
May 14, 2026

2025 – 2026

United States locations

U.S. sites
46
U.S. states
24
U.S. cities
45
Facility City State ZIP Site status
Associated Retina Consultants Gilbert Arizona 85297 —
Associated Retina Consultants, Ltd. Phoenix Arizona 85020 —
Phoenix Retina Associates Phoenix Arizona 85050 —
Retina Macula Institute of Arizona Scottsdale Arizona 85255 —
Global Research Management Glendale California 91204 —
Retina Associates of Southern California Huntington Beach California 92647 —
Retinal Consultants Medical Group, Inc Modesto California 95356 —
Eye Research Foundation Newport Beach California 92663 —
Retina Consultants of San Diego Poway California 92064 —
Retinal Consultants Medical Group Sacramento California 95825 —
Bay Area Retina Associates - Walnut Creek Walnut Creek California 94598 —
Colorado Retina Associates Lakewood Colorado 80228 —
Connecticut Eye Consultants, PC Danbury Connecticut 06810 —
Retina Group of New England, PC Waterford Connecticut 06385 —
Rand Eye Institute Deerfield Beach Florida 33064 —
Retina Group of Florida Fort Lauderdale Florida 33308 —
Eye Associates of Pinellas Pinellas Park Florida 33782 —
Retina Vitreous Associates of Florida St. Petersburg Florida 33711 —
Southeast Retina Center, PC Augusta Georgia 30909 —
University Retina and Macula Associates Lemont Illinois 60439 —
Illinois Retina Associates - Oak Park Oak Park Illinois 60304 —
Butchertown Clinical Trials Louisville Kentucky 40206 —
Mid Atlantic Retina Specialists Hagerstown Maryland 21740 —
Ophthalmic Consultants of Boston Boston Massachusetts 02114 —
Retina Consultants of Minnesota Edina Minnesota 55435 —
Mississippi Retina Associates Madison Mississippi 39110 —
University of Missouri Health System Columbia Missouri 65212 —
Envision Ocular, LLC Bloomfield New Jersey 07003 —
Eye Associates of New Mexico Albuquerque New Mexico 87109 —
Long Island Vitreoretinal Consultants - Westbury Westbury New York 11590 —
Verum Research, LLC Eugene Oregon 97401 —
Mid Atlantic Retina - Bethlehem Bethlehem Pennsylvania 18017 —
Charleston Neuroscience Institute - Charleston Charleston South Carolina 29414 —
Tennessee Retina Nashville Tennessee 37203 —
Austin Clinical Research, LLC Austin Texas 78750 —
Retina Consultants of Texas-Beaumont-70319 Beaumont Texas 77707 —
Retina Consultants of Texas-Bellaire-67493 Bellaire Texas 77401 —
Retina Foundation of the Southwest Dallas Texas 75231 —
Retina Consultants of Texas - Katy Katy Texas 77494 —
Red River Research Partners, LLC Plano Texas 75024 —
Retinal Consultants of San Antonio San Antonio Texas 78240 —
Retina Consultants of Texas - Schertz Schertz Texas 78154 —
Retina Consultants of Texas-The Woodlands-67575 The Woodlands Texas 77384 —
Retina Associates of Utah Salt Lake City Utah 84107 —
Piedmont Eye Center Lynchburg Virginia 24502 —
Spokane Eye Clinic 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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06722157, 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 May 14, 2026 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06722157 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →