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

Status unknown · Phase 4 · NCT05322070

Conditions: Uveitis, Posterior

At a glance

Research payments reported, 2025
$161,074
U.S. investigators named
14
Sites paid
13
Planned or actual enrollment
125

About the trial

Sponsor
Alimera Sciences (with CBCC Global Research)
Tested
Fluocinolone Acetonide Intravitreal Implant 0.18 mg (drug)
Dates
Started 2022-06-06; completion 2025-11
Results posted
Not yet

A study to evaluate the safety and efficacy of YUTIQ® 0.18 mg intravitreal implant for the management of chronic non-infectious posterior segment uveitis (intraocular inflammation) that has responded to previous steroid therapy.

From ClinicalTrials.gov, last updated 2024-08-06. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Ani Pharmaceuticals, Inc. reported $161,074 in research payments for this study in 2025 (75 payments).

Products named: Yutiq

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

  • Illinois Retina Associates $31,633
  • Tennessee Retina PC $28,802
  • Retina Group of Florida $23,499
  • Retina Consultants of Texas $21,023
  • The Clinical Trials Network LLC $16,809
  • Vitreo-Retinal Medical Group Inc Vrmg $10,908
  • Macula and Retina Institute $10,350
  • Retina Specialist of Tampa $7,837
  • Foundation of Vision Research $3,698
  • Midwest Vision Research Foundation $2,986
  • Cumberland Valley Retina Consultants $1,250
  • Azul Vision $1,250
  • Colorado Retina Associates $1,028

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.