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Active, not recruiting Phase 4 Interventional

Fluocinolone Acetonide Intravitreal Implant 0.18 mg in the Treatment of Chronic Non-Infectious Posterior Segment Uveitis

ClinicalTrials.gov ID: NCT05322070

Public ClinicalTrials.gov record NCT05322070. 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, 4:54 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

Phase 4 Study of YUTIQ® (Fluocinolone Acetonide Intravitreal Implant) 0.18 mg in the Treatment of Chronic Non-Infectious Posterior Segment Uveitis (Intraocular Inflammation Study)

Study identification

NCT ID
NCT05322070
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 4
Lead sponsor
Alimera Sciences
Industry
Enrollment
125 participants

Conditions and interventions

Interventions

  • Fluocinolone Acetonide Intravitreal Implant 0.18 mg Drug

Drug

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
Jun 5, 2022
Primary completion
Oct 31, 2025
Completion
Oct 31, 2025
Last update posted
Aug 5, 2024

2022 – 2025

United States locations

U.S. sites
23
U.S. states
14
U.S. cities
23
Facility City State ZIP Site status
Retina Consultants of Orange County Fullerton California 92835
Macula and Retina Institute Glendale California 91203
California Eye Specialists Medical Group Pasadena California 91107
Retinal Consultants Medical Group Sacramento California 95825
Retina Associates of Colorado Lakewood Colorado 80228
Advanced Research Coral Springs Florida 33067
Retina Specialists of Tampa Wesley Chapel Florida 33544
Marietta Eye Clinic Marietta Georgia 30060
Retinal Vitreal Consultants Ltd. Chicago Illinois 60616
Illinois Retina Associates, S.C. Oak Park Illinois 60304
Cumberland Valley Retina Consultants Hagerstown Maryland 21740
Opthalmic Consultants of Boston Boston Massachusetts 02114
Massachusets Eye Research and Surgery Institution Waltham Massachusetts 02451
Foundation for Vision Research Grand Rapids Michigan 49546
Midwest Vision Research Foundation at Pepose Vision Institute Chesterfield Missouri 63017
Retina Consultants Fargo North Dakota 58104
Retina Vitreous Associates Toledo Ohio 43623
Erie Retina Research, LLC Erie Pennsylvania 16507
Tennessee Retina Nashville Tennessee 37203
Retina Consultants of Texas Bellaire Texas 77401
Retina Consultants of Texas Katy Texas 77494
Valley Retina Institute, PA McAllen Texas 78503
Medical Center Opthalmology Associates San Antonio Texas 78240

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 NCT05322070, 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 Aug 5, 2024 · Synced Jul 22, 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 protocol, eligibility criteria, and contact information for NCT05322070 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →