Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

A Proof-of-Concept Study of Faricimab (RO6867461) in Participants With Choroidal Neovascularization (CNV) Secondary to Age-Related Macular Degeneration (AMD)

ClinicalTrials.gov ID: NCT02484690

Public ClinicalTrials.gov record NCT02484690. 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 21, 2026, 6:22 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 Multiple-Center, Multiple-Dose and Regimen, Randomized, Active Comparator Controlled, Double-Masked, Parallel Group, 36 Week Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Efficacy of RO6867461 Administered Intravitreally in Patients With Choroidal Neovascularization Secondary to Age-Related Macular Degeneration

Brief summary

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

This multiple-center, multiple-dose and regimen, randomized, double-masked active comparator-controlled, double-masked, five parallel group, 36-week study will evaluate the efficacy, safety, tolerability, and pharmacokinetics of faricimab (RO6867461) in participants with choroidal neovascularization (CNV) secondary to age-related macular degeneration (AMD). The study was designed to allow the evaluation of RO6867461 in a treatment-naive population (comparison of Arms A, B, C, and D) and an anti-VEGF-incomplete responder population that met a predefined criterion at Week 12 (comparison between Arms A and E). Only one eye per participant was chosen as the study eye.

Study identification

NCT ID
NCT02484690
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
273 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
Aug 11, 2015 (Actual)
Primary completion
Sep 26, 2017 (Actual)
Completion
Sep 26, 2017 (Actual)
Last update posted
Nov 12, 2020

2015 – 2017

United States locations

U.S. sites
52
U.S. states
24
U.S. cities
49
Facility City State ZIP Site status
Associated Retina Consultants Phoenix Arizona 85020 —
Retinal Consultants of Arizona Phoenix Arizona 85053 —
California Retina Consultants Bakersfield California 93309 —
Retina-Vitreous Associates Medical Group Beverly Hills California 90211 —
The Retina Partners Encino California 91436 —
Retina Consultants, San Diego Poway California 92064 —
Orange County Retina Med Group Santa Ana California 92705 —
Bay Area Retina Associates Walnut Creek California 94598 —
American Institute of Research Whittier California 90603 —
Retina Consultants of Southern Colorado Springs Colorado 80909 —
Colorado Retina Associates, PC Golden Colorado 80401 —
New England Retina Associates Hamden Connecticut 06518 —
Retina Health Center Fort Myers Florida 33907 —
National Ophthalmic Research Institute Fort Myers Florida 33912 —
Florida Eye Associates Melbourne Florida 32901 —
Central Florida Retina Orlando Florida 32806 —
Retina Care Specialists Palm Beach Gardens Florida 33410 —
Retina Vitreous Assoc of FL St. Petersburg Florida 33711 —
Southern Vitreoretinal Assoc Tallahassee Florida 32308 —
Southeast Retina Center Augusta Georgia 30909 —
Georgia Retina PC Marietta Georgia 30060 —
Midwest Eye Institute Northside Indianapolis Indiana 46290 —
Paducah Retinal Center Paducah Kentucky 42001 —
Retina Group of Washington Chevy Chase Maryland 20815 —
National Retina Institute Towson Maryland 21204 —
Vitreo-Retinal Associates, PC Worcester Massachusetts 01605 —
Vitreoretinal Surgery Edina Minnesota 55435 —
Retina Associates of NJ Toms River New Jersey 08755 —
Eye Associates of New Mexico Albuquerque New Mexico 87102 —
Long Is. Vitreoretinal Consult Great Neck New York 11021 —
Opthalmic Consultants of LI Lynbrook New York 11563 —
Retina Assoc of Western NY Rochester New York 14620 —
The Retina Consultants Slingerlands New York 12159 —
Western Carolina Retinal Associate PA Asheville North Carolina 28803 —
Char Eye Ear &Throat Assoc Charlotte North Carolina 28210 —
OSU Eye Physicians & Surgeons Columbus Ohio 43212 —
Oregon Retina, LLP Eugene Oregon 97401 —
Oregon Retina institute Medford Oregon 97504 —
Retina Northwest Portland Oregon 97221 —
Mid Atlantic Retina Philadelphia Pennsylvania 19107 —
Palmetto Retina Center West Columbia South Carolina 29169 —
Southeastern Retina Associates Chattanooga Chattanooga Tennessee 37421 —
Charles Retina Institute Germantown Tennessee 38138 —
Tennessee Retina PC. Nashville Tennessee 37203 —
W Texas Retina Consultants PA Abilene Texas 79606 —
Austin Retina Associates Austin Texas 78705 —
Retina Research Center Austin Texas 78705 —
Retina Consultants of Houston Houston Texas 77030 —
Strategic Clinical Research Group, LLC Willow Park Texas 76087 —
Retina Associates of Utah Salt Lake City Utah 84107 —
Univ of Virginia Ophthalmology Charlottesville Virginia 22903 —
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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02484690, 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 Nov 12, 2020 · Synced Oct 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02484690 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →