Användningen av två YUTIQ kontra bluff för behandling av kronisk icke-infektiös intraokulär inflammation som påverkar det bakre segmentet (TYNI)

Inclusion Criteria:

General Inclusion Criteria:

1. Male or non-pregnant female in good general health at least 18 years of age, understands the language of the informed consent, and is willing and able to provide written informed consent and sign/date a health information release (HIPAA form) before any study procedures are performed.
2. Willingness and ability to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures.

Ocular Inclusion Criteria (Study Eye):

1. Diagnosed with chronic unilateral or bilateral noninfectious posterior segment inflammation (with or without anterior uveitis) that demonstrated a clinical response to ≥1 previous corticosteroid treatment of any localized type (eg, topical steroid 2 to 4 times per day or intra- or peri-ocular injection) or systemic corticosteroid/immunosuppressant treatment with recurrence following treatment indicating chronicity according to the Investigator's judgment.
2. Presence of active posterior segment inflammation as determined by the Investigator.
3. Vitreous haze grade ≥ 2 based on the standardization of uveitis nomenclature (SUN) criteria.
4. Less than 10 anterior chamber cells/high power field determined by slit lamp examination.
5. Not planning to undergo elective ocular surgery during the study.

Exclusion Criteria:

General Exclusion Criteria:

1. Subjects with known hypersensitivity to any components of YUTIQ.
2. Female subjects who are pregnant or breastfeeding.
3. Has any acute or chronic medical disease or psychiatric condition that, in the opinion of the Investigator, would preclude participation in the study or put the subject at risk due to study treatment or procedures.

Ocular Exclusion Criteria (Study Eye):

1. History of anterior uveitis only (without associated uveitis that affected the posterior segment).
2. Presence of a vitreous hemorrhage.
3. Uveitis with infectious etiology.
4. Intraocular inflammation associated with a condition other than non-infectious uveitis (e.g., intraocular lymphoma).
5. Current infectious diseases of the cornea and conjunctiva, mycobacterial infections of the eye, or fungal diseases of ocular structures.
6. Subjects with ACIOL (Anterior Chamber Intraocular Lens) or rupture of the posterior lens capsule.
7. Diagnosis of any form of glaucoma or ocular hypertension at screening, unless the study eye is being treated with ≤2 intraocular pressure (IOP)-lowering medications and/or has been previously treated with an incisional surgical procedure resulting in stable IOP in the normal range (10 to 21 mmHg).
8. Intraocular pressure >21 mmHg or concurrent therapy at screening with >2 IOP-lowering pharmacologic agents in the study eye.
9. Any eye surgery within 12 weeks prior to Day 1 of the study.
10. Subjects who are unable to attend scheduled follow-up visits throughout the 12-month study.
11. Has a significant media opacity precluding evaluation of retina and vitreous in the study eye.