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Completed Phase 3 Interventional

A Study to Investigate Vamikibart in Participants With Uveitic Macular Edema

ClinicalTrials.gov ID: NCT05642312

Public ClinicalTrials.gov record NCT05642312. 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 30, 2026, 2:10 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 Phase III, Multicenter, Randomized, Double-Masked, Sham-Controlled Study to Investigate the Efficacy, Safety, Pharmacokinetics and Pharmacodynamics of Vamikibart Administered Intravitreally in Patients With Uveitic Macular Edema

Brief summary

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

This study will assess the efficacy and safety of vamikibart in participants with uveitic macular edema.

Study identification

NCT ID
NCT05642312
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
245 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 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 9, 2023 (Actual)
Primary completion
Dec 9, 2024 (Actual)
Completion
Jul 9, 2025 (Actual)
Last update posted
Nov 21, 2025

2023 – 2025

United States locations

U.S. sites
16
U.S. states
14
U.S. cities
16
Facility City State ZIP Site status
Kaiser Permanente Southern California Los Angeles California 90027 —
Colorado Retina Associates, PC Lakewood Colorado 80228 —
Retina Vitreous Associates of Florida St. Petersburg Florida 33711-1141 —
Cumberland Valley Retina PC Hagerstown Maryland 21740 —
VitreoRetinal Surgery, PLLC. Minneapolis Minnesota 55435 —
Truhlsen Eye Institute Omaha Nebraska 68106-5540 —
Envision Ocular, LLC Bloomfield New Jersey 07003 —
Wake Forest Baptist Health Eye Centre Winston-Salem North Carolina 27157 —
University Hospitals Cleveland Medical Center Cleveland Ohio 44106 —
The Ohio State University Investigational Drug Services Columbus Ohio 43212 —
Oregon Health & Science Uni Portland Oregon 97239 —
Erie Retina Research Erie Pennsylvania 16507-1429 —
Palmetto Retina Center West Columbia South Carolina 29169 —
Tennessee Retina PC Nashville Tennessee 37203 —
Austin Clinical Research LLC Austin Texas 78750 —
Texas Retina Associates Dallas Texas 75231 —

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 61 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05642312, 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 21, 2025 · Synced Oct 30, 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 NCT05642312 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →