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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 Jul 22, 2026, 12:23 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

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

  • Vamikibart Drug
  • Sham Other

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 8, 2023
Primary completion
Dec 8, 2024
Completion
Jul 8, 2025
Last update posted
Nov 20, 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 20, 2025 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05642312 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →