Uveitis Clinical Trial
— TYNIOfficial title:
The Use of Two YUTIQ Versus Sham for Treatment of Chronic Non Infectious Intraocular Inflammation Affecting the Posterior Segment (TYNI Trial)
The Use of Two YUTIQ versus Sham for Treatment of Chronic Non Infectious Intraocular Inflammation Affecting the Posterior Segment (TYNI Trial)
Status | Recruiting |
Enrollment | 30 |
Est. completion date | December 2024 |
Est. primary completion date | December 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | 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. |
Country | Name | City | State |
---|---|---|---|
United States | Texas Retina Associates | Plano | Texas |
Lead Sponsor | Collaborator |
---|---|
Texas Retina Associates | Eye Point Pharmaceuticals |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Recurrence rate of uveitis will be assessed at the 6-month visit | The primary endpoint of recurrence rate of uveitis will be assessed at the 6-month visit. The clinical definition of intraocular inflammation recurrence is (1) a 2-step or more increase in number of cells in the anterior chamber per high-powered field (x1.6 using a 1-mm beam), (2) a 2-step or more increase in vitreous haze, or (3) a deterioration in BCVA of 15 letters or more. In each case, the etiology of the change must be only due to noninfectious uveitis. | 6 months | |
Secondary | Recurrence rate of uveitis at the 12-month visit | The secondary endpoints include determining the recurrence rate of uveitis at the 12-month visit, time to first uveitis recurrence, change in BCVA from baseline by ETDRS letters read at the 12-month visit, total number of necessary adjunctive treatments necessary, mean changes in CST as measured by SD-OCT, and mean changes from baseline in BCVA by ETDRS letters read. A final secondary endpoint will be to evaluate the changes in vascular leakage on FA, which will qualitatively be determined by the investigator. | 12 months |
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