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

Alimera Sciences

Status and phase

Active, not recruiting

Phase 4

Conditions

Uveitis, Posterior

Treatments

Drug: Fluocinolone Acetonide Intravitreal Implant 0.18 mg

Study type

Interventional

Funder types

NETWORK

Industry

Identifiers

NCT05322070

EYP-YUT-002

Details and patient eligibility

About

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.

Full description

This is a prospective, phase 4, open-label, uncontrolled, 2-year follow-up study to evaluate the safety and efficacy of YUTIQ® (fluocinolone acetonide intravitreal implant) 0.18 mg for the management of chronic non-infectious posterior segment uveitis (intraocular inflammation) that has responded to previous steroid therapy. Patients will receive YUTIQ® 0.18 mg as an intravitreal injection in the designated study eye and will be followed for 24 months after treatment.

Enrollment

125 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Male or female in good general health at least 18 years of age at time of consent.
Presence of active, recurrent, unilateral or bilateral non-infectious uveitis affecting the posterior segment (intraocular inflammation) with a duration of at least 3 months from initial diagnosis, as determined by the Investigator. Intermediate or panuveitis will also be allowed if posterior segment involvement is part of the diagnosis.
Posterior segment inflammation that has previously demonstrated a clinical response to ≥1 localized corticosteroid treatment (eg, topical steroid 2 to 4 times per day or intra- or peri-ocular injection).
Presence of macular edema as measured by spectral-domain - optical coherence tomography (SD-OCT) (≥325 microns on Heidelberg SPECTRALIS and ≥315 microns on Zeiss CIRRUS).
Best corrected visual acuity (BCVA) of the study eye 35-75 letters on the ETDRS chart (Snellen range 20/30 to 20/200).
Not planning to undergo elective ocular surgery during the study.
Able to understand, sign the Informed Consent Form (ICF).
Willingness and ability to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures.

Exclusion criteria

History of macular edema due to diabetes, retinal vein occlusion (RVO), age-related macular degeneration (AMD), or any non-inflammatory cause.
Intraocular inflammation with infectious etiology.
Diagnosis of uncontrolled glaucoma or ocular hypertension at Screening, unless study eye is being treated with ≤2 intraocular pressure (IOP)-lowering medications and/or has been previously treated with an incisional surgical procedure OR glaucoma laser procedure resulting in stable IOP in the normal range (10 to 21 mmHg).
Intraocular pressure >21 mmHg or concurrent therapy at Screening with >2 IOP-lowering pharmacologic agents in the study eye.
Ocular malignancy in either eye, including choroidal melanoma.
Previous viral retinitis.
Toxoplasmosis scar or scar related to previous viral retinitis in the study eye.
Ocular and periocular infections such as diseases of the cornea and conjunctiva including epithelial herpes simplex keratitis (dendritic keratitis), vaccinia, and varicella, mycobacterial infections of the eye, or fungal diseases of ocular structures.
Hypersensitivity to any of the ingredients contained in YUTIQ®.
Media opacity precluding evaluation of retina and vitreous (eg, vitreous hemorrhage).
Any current retinal detachment or retinoschisis in insertion in the study eye.
Chronic hypotony, defined as <6 mmHg for at least 1 month's duration, and documented on at least two separate visits.
Ocular surgery within 12 weeks prior to Day 1.
YAG laser capsulotomy within 30 days prior to Day 1.
Prior intravitreal treatment with Retisert®, ILUVIEN®, or YUTIQ® (0.18 mg) within 36 months prior to Day 1.
Prior intravitreal treatment with OZURDEX® within 12 weeks prior to Day 1.
Prior intravitreal treatment with Triesence® or TRIVARIS™ (triamcinolone) within 12 weeks prior to Day 1.
Peri-ocular or subtenon steroid treatment within 12 weeks prior to Day 1.
Radiation to the head or neck within 2 years prior to Screening.
Steroid allergy, particularly to fluocinolone.
Any systemic condition that requires chronic systemic anti-inflammatory, steroid, or immunosuppressive therapy (subjects on a stable dose of oral prednisone <7.5 mg per day for a non-ocular indication may be included).
Positive test for human immunodeficiency virus (HIV), tuberculosis, or syphilis in the past 2 years or during Screening.
Any severe acute or chronic medical (eg, cancer diagnosis) or psychiatric condition that could increase the risk associated with study participation or could interfere with the interpretation of study results and make the subject inappropriate for study enrollment.
Any other systemic or ocular condition which, in the judgment of the Investigator, could make the subject inappropriate for study enrollment.
Treatment with an investigational drug or device within 30 days prior to Day 1.
Pregnant or nursing females; females of childbearing potential who are unwilling or unable to use an acceptable method of contraception as outlined in the protocol from at least 14 days prior to Day 1 until the final study visit.