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Completed Phase 3 Interventional Results available

Safety and Efficacy of an Injectable Fluocinolone Acetonide Intravitreal Insert

ClinicalTrials.gov ID: NCT01694186

Public ClinicalTrials.gov record NCT01694186. 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, 5:55 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, Multi-National, Multi-Center, Randomized, Masked, Controlled, Safety and Efficacy Study of a Fluocinolone Acetonide Intravitreal Insert in Subjects With Chronic Non-Infectious Uveitis Affecting the Posterior Segment of the Eye

Study identification

NCT ID
NCT01694186
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
EyePoint Pharmaceuticals, Inc.
Industry
Enrollment
129 participants

Conditions and interventions

Interventions

  • FAI insert Drug
  • Sham injection 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
Aug 1, 2013
Primary completion
Mar 25, 2018
Completion
Mar 25, 2018
Last update posted
Apr 1, 2021

2013 – 2018

United States locations

U.S. sites
16
U.S. states
12
U.S. cities
16
Facility City State ZIP Site status
Retina Vitreaous Associates Beverly Hills California 90211
Retinal Consultants Medical Group, Inc Sacramento California 95819
Retina Macula Institute Torrance California 90503
Retina Consultants of Southern Colorado Colorado Springs Colorado 80909
Northwestern University Chicago Illinois 60611
Ophthalmology & Visual Sciences Lexington Kentucky 40508
Ocular Immunology and Uveitis Foundation Cambridge Massachusetts 02142
University of Nebraska Medical Center Omaha Nebraska 68198
Retina Consultants Slingerlands New York 12159
Duke University Eye Center Durham North Carolina 27710
Cleveland Clinic Cleveland Ohio 44195
OHSU Casey Eye Institute Portland Oregon 97239
Charleston Neuroscience Institute Ladson South Carolina 29456
Texas Retina Associates Arlington Texas 76012
Retina Consultants of Houston Houston Texas 77030
Foresight Studies, LLC 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.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 18 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01694186, 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 Apr 1, 2021 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01694186 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →