Ustekinumab for Active Sight-Threatening Uveitis
- Sponsor
- National Eye Institute (NEI)
- Study ID
- NCT01647152
- Phase
- PHASE1/PHASE2
- Status
- Withdrawn
Conditions
- Uveitis
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Ustekinumab — DRUG
Study Details
Background: \- Uveitis is an eye inflammation that can cause vision loss. It is treated with eye drops, drugs and sometimes surgery. In some people, treatment may not prevent vision loss. A type of white blood cells called T-cells often have a role in causing uveitis. In some cases of uveitis, T-cells attack the eye and cause inflammation. A drug called ustekinumab reduces inflammation from these T-cells. Researchers want to see if ustekinumab can be used to treat uveitis. Objectives: \- To see if ustekinumab can be used to treat uveitis. Eligibility: \- Individuals at least 18 years of age who have active uveitis that needs treatment. Design: * Participants will be screened with a physical exam, eye exam, and medical history. Blood and urine samples will be taken. * Participants will have at least eight clinic visits during the 64-week study period. After the first visit, visits will occur at 2, 4, and 8 weeks, and then every 12 weeks. * Participants will have a ustekinumab injection at the first study visit. They will have additional doses at the second and third visits, and then every 12 weeks until 1 year after the first dose (Week 52). * Treatment will be monitored with frequent blood tests and eye exams. Other standard treatments for uveitis may be given as needed. * There will be a final study visit 3 months after the last injection.
Key Dates
- Start date
- Jul 3, 2012
- Status verified
- Sep 2014
- Primary completion
- Jun 30, 2015
- Completion
- Jun 30, 2015
Study Design
- Enrollment
- 0 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Primary Outcome Measure
The primary outcome is the number of participants who experience at least a 2-step (or down to grade 0) reduction in inflammation as per the Standardization of Uveitis Nomenclature (SUN) criteria by Week 8.
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