Yutiq (fluocinolone acetonide intravitreal implant) / EyePoint Pharma 
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  • ||||||||||  Journal:  Intravitreal steroid implants in the management of noninfectious intermediate and posterior uveitis. (Pubmed Central) -  Sep 22, 2024   
    Dexamethasone implants favor the therapeutic goal of prevention of recurrences, whereas the use of fluocinolone implants helps to attain better visual outcomes due to their longer duration of action. Thus, the review provides recent literature supporting the role and indication of sustained release intravitreal implants in the management of noninfectious intermediate and posterior uveitis.
  • ||||||||||  Yutiq (fluocinolone acetonide intravitreal implant) / EyePoint Pharma, Iluvien (fluocinolone acetonide) / Alimera Sci, EyePoint Pharma
    Review, Journal:  Fluocinolone acetonide 0.2 (Pubmed Central) -  May 30, 2024   
    As more clinical experience has been gained using FAc implants, it was necessary to update the clinical recommendations that guide patient management in the clinic. The current consensus document addresses relevant issues related to the use of FAc implants on different types of patients with various etiologies of NIU-PS, and was conducted to standardize approaches to help specialists obtain better clinical outcomes.
  • ||||||||||  Ozurdex (dexamethasone intravitreal implant) / AbbVie, Xipere (triamcinolone acetonide) / Clearside Biomedical, Bausch Health, Arctic Vision, Yutiq (fluocinolone acetonide intravitreal implant) / EyePoint Pharma
    Improvement of Postoperative Macular Edema Following Intravitreal Steroid Injections (POSTER THEATER) -  Oct 28, 2023 - Abstract #AAO2023AAO_1661;    
    CST and MV improved significantly at 6 weeks (?129 ?m, P ? 10-13; ?0.88 mm
  • ||||||||||  Yutiq (fluocinolone acetonide intravitreal implant) / EyePoint Pharma
    Trial termination, Trial primary completion date:  Safety and Efficacy of an Injectable Fluocinolone Acetonide Intravitreal Insert (FAI) (clinicaltrials.gov) -  Sep 8, 2023   
    P3,  N=12, Terminated, 
    10-13; ?0.88 mm Active, not recruiting --> Terminated | Trial primary completion date: Apr 2023 --> Oct 2022; No longer pursuing indication
  • ||||||||||  Yutiq (fluocinolone acetonide intravitreal implant) / EyePoint Pharma
    Enrollment closed, Enrollment change, Trial primary completion date:  Safety and Efficacy of an Injectable Fluocinolone Acetonide Intravitreal Insert (FAI) (clinicaltrials.gov) -  Dec 21, 2022   
    P3,  N=12, Active, not recruiting, 
    Active, not recruiting --> Terminated | Trial primary completion date: Apr 2023 --> Oct 2022; No longer pursuing indication Recruiting --> Active, not recruiting | N=60 --> 12 | Trial primary completion date: Oct 2022 --> Apr 2023
  • ||||||||||  Yutiq (fluocinolone acetonide intravitreal implant) / EyePoint Pharma
    New trial:  A Study of YUTIQ (clinicaltrials.gov) -  Oct 25, 2022   
    P=N/A,  N=15, Recruiting, 
  • ||||||||||  Yutiq (fluocinolone acetonide intravitreal implant) / EyePoint Pharma
    Journal, Monotherapy:  Efficacy of the Fluocinolone Acetonide (Yutiq) Intravitreal Implant as Monotherapy for Uveitis. (Pubmed Central) -  Jul 7, 2022   
    The fluocinolone acetonide implant may not suffice as monotherapy for all patients with uveitis, but it may be effective as an adjunctive treatment. We propose a clinical workflow for the selection and treatment of patients who may benefit from it.
  • ||||||||||  Yutiq (fluocinolone acetonide intravitreal implant) / EyePoint Pharma
    Journal:  Preliminary evaluation of YUTIQ™ (fluocinolone acetonide intravitreal implant 0.18 mg) in posterior uveitis. (Pubmed Central) -  Jun 9, 2020   
    The treatment goal is to target the site of inflammation with low dose of corticosteroids, delivered over an extended period of time, to minimize the cumulative damage resulting from repeated recurrences, reducing both injections frequency and ocular side effects. This article will review the pharmacology and preliminary clinical data of the 0.18 mg fluocinolone acetonide intravitreal implant (YUTIQ™), to show its efficacy and safety in the treatment of noninfectious posterior uveitis.