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Clinical trialNCT01694186CompletedPhase 3Interventional

Safety and Efficacy of an Injectable Fluocinolone Acetonide Intravitreal Insert

SponsorEyePoint Pharmaceuticals, Inc.Enrollment129Non-Infectious Uveitis
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

A study to evaluate the safety and efficacy of an FAI insert for the management of subjects with non-infectious uveitis affecting the posterior segment of the eye.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

34 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Germany
  • Augenarzte Am St. Franziskus Hospital

    Münster, Germany

  • Universitatsklinikum Tubingen

    Tübingen, Germany

Hungary
  • Bajcsy-Zsilinszky Kórház És Rendelőintézet

    Budapest, Hungary

India
  • L. V. Prasad Eye Institute - Hospital

    Hyderabad, Andhra Pradesh, India

  • L.V. Prasad Eye Institute

    Patia, Bhubaneshwar, India

  • C.H Nagri Municipal Eye Hospital

    Ahmedabad, Gujarat, India

  • Seth G.S. Medical College & Kem Hospital

    Pārel, Mumbai, India

  • Pbma'S H.V. Desai Eye Hospital

    Hadapsar, Pune, India

  • King George'S Medical University

    Lucknow, Uttar Pradesh, India

Israel
  • Hadassah University Hospital Ein Kerem

    Jerusalem, Israel

  • Rabin Medical Center

    Petah Tikva, Israel

  • Sheba Medical Center

    Qiryat Ono, Israel

United Kingdom
  • Royal Hospitals Trust

    Belfast, United Kingdom

  • Birmingham and Midland Eye Centre

    Birmingham, United Kingdom

  • Bradford Royal Infirmary

    Bradford, United Kingdom

  • Gloucestershire Royal Hospital

    Gloucester, United Kingdom

  • Moorfields Eye Hospital

    London, United Kingdom

  • St Thomas Hospital

    London, United Kingdom

United States
  • Retina Vitreaous Associates

    Beverly Hills, California, United States

  • Retinal Consultants Medical Group, Inc

    Sacramento, California, United States

  • Retina Macula Institute

    Torrance, California, United States

  • Retina Consultants of Southern Colorado

    Colorado Springs, Colorado, United States

  • Northwestern University

    Chicago, Illinois, United States

  • Ophthalmology & Visual Sciences

    Lexington, Kentucky, United States

  • Ocular Immunology and Uveitis Foundation

    Cambridge, Massachusetts, United States

  • University of Nebraska Medical Center

    Omaha, Nebraska, United States

  • Retina Consultants

    Slingerlands, New York, United States

  • Duke University Eye Center

    Durham, North Carolina, United States

  • Cleveland Clinic

    Cleveland, Ohio, United States

  • Ohsu Casey Eye Institute

    Portland, Oregon, United States

  • Charleston Neuroscience Institute

    Ladson, South Carolina, United States

  • Texas Retina Associates

    Arlington, Texas, United States

  • Retina Consultants of Houston

    Houston, Texas, United States

  • Foresight Studies, Llc

    San Antonio, Texas, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

FAI insertSham injection
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
2 Aug 2013
Primary completion
26 Mar 2018
Completion
26 Mar 2018
Last update posted
2 Apr 2021
Registered enrollment
129
Registry id
NCT01694186

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.