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Uveitis clinical trials

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NCT ID: NCT04088409 Active, not recruiting - Uveitis Clinical Trials

A Study of Baricitinib (LY3009104) in Participants From 2 Years to Less Than 18 Years Old With Active JIA-Associated Uveitis or Chronic Anterior Antinuclear Antibody-Positive Uveitis

Start date: October 16, 2019
Phase: Phase 3
Study type: Interventional

The reason for this study is to see if the study drug baricitinib given orally is safe and effective in participants with active juvenile idiopathic arthritis (JIA)-associated uveitis or chronic anterior antinuclear antibody-positive uveitis from 2 years to less than 18 years old.

NCT ID: NCT03889860 Active, not recruiting - Uveitis Clinical Trials

Objective Choroidal Thickness Measurements in Uveitis

Start date: September 1, 2018
Phase:
Study type: Observational

Optical Coherence Tomography (OCT) machines are non-contact instruments that can provide micrometer scale imaging of biological tissue. Applying the image processing allows us to automatically measure the choroidal thickness with good interclass correlation coefficient to the manual measurements.

NCT ID: NCT03828019 Active, not recruiting - Uveitis Clinical Trials

Adalimumab vs. Conventional Immunosuppression for Uveitis Trial

ADVISE
Start date: September 16, 2019
Phase: Phase 3
Study type: Interventional

Non-infectious intermediate, posterior, and panuveitides are chronic, potentially-blinding diseases. Vision-threatening cases require long-term therapy with oral corticosteroids and immunosuppression. Based upon preliminary data, adalimumab, a fully-human, anti-TNF-α monoclonal antibody, now US FDA-approved for uveitis treatment, may be a superior corticosteroid-sparing agent than conventional immunosuppressive drugs. The ADVISE Trial is multicenter randomized, parallel-treatment, comparative effectiveness trial comparing adalimumab to conventional (small molecule) immunosuppression for corticosteroid spring in the treatment of non-infectious, intermediate, posterior, and panuveitides.

NCT ID: NCT03816397 Active, not recruiting - Uveitis Clinical Trials

Adalimumab in JIA-associated Uveitis Stopping Trial

ADJUST
Start date: March 15, 2020
Phase: Phase 4
Study type: Interventional

The proposed study is a stratified, block-randomized, double-masked, controlled trial to determine the feasibility of discontinuing adalimumab treatment in patients with quiescent uveitis associated with juvenile idiopathic arthritis (JIA) or chronic anterior uveitis (CAU).

NCT ID: NCT03634475 Active, not recruiting - Clinical trials for Non-infectious Uveitis

A Safety Study of Intravitreal PP-001 in Patients With Chronic, Non-Infectious Uveitis

Start date: January 2017
Phase: Phase 1/Phase 2
Study type: Interventional

In this study, PP-001 is assessed for safety and efficacy in patients diagnosed with non-infectious chronic uveitis. PP-001 is a novel small molecule that inhibits a specific enzyme (Dihydroorotate Dehydrogenase) and has shown pre-clinical efficacy in treatment of non-infectious uveitis. PP-001 will be administered to participants as a single intravitreal injection in ascending doses.

NCT ID: NCT03580343 Active, not recruiting - Uveitis Clinical Trials

Tofacitinib for Inflammatory Eye Disease

Start date: April 4, 2019
Phase: Phase 2
Study type: Interventional

Non-infectious inflammatory eye disease, such as uveitis and scleritis, is a chronic, auto-immune process that leads to vision loss. While steroids are effective in the short term, the side-effect profile of chronic steroid use necessitates the identification of effective steroid-sparing therapies. Tofacitinib is a small molecule that inhibits the signaling pathways of multiple inflammatory cytokines. The investigators plan to evaluate whether tofacitinib may have efficacy for patients with uveitis and / or scleritis.

NCT ID: NCT02943057 Active, not recruiting - Clinical trials for Cytomegalovirus Infections

Topical 2% Ganciclovir Eye Drop for CMV Anterior Uveitis / Endotheliitis

Start date: October 2016
Phase: Phase 4
Study type: Interventional

25 patients who are diagnosed with Cytomegalovirus (CMV) anterior segment infection, either uveitis or endotheliitis, will be started on 2% guttae ganciclovir, 1 drop 5 times a day for 6 weeks. Following 6 weeks of continuous application of 2% guttae ganciclovir, patient will be reviewed at the clinic within 3 hours following the last application of topical ganciclovir and clinical features will be documented for activity assessment. An aqueous sample 0.2ml is drawn. 0.1ml will be sent for RT-PCR for CMV viral load and another 0.1ml will be sent for ganciclovir drug level by HPLC method.

NCT ID: NCT02252328 Active, not recruiting - Uveitis Clinical Trials

Use of Simvastatin as a Steroid Sparing Agent for Uveitis Patients

Start date: September 2015
Phase: Phase 2/Phase 3
Study type: Interventional

The trial will compare the effect on disease control and immunosuppression treatment of adding simvastatin 80mg once daily, over a follow-up and treatment period of 2 years. Patients will be randomised in a 1:1 fashion to standard treatment with placebo or standard treatment with the addition of simvastatin (80mg daily). They will be followed at 3 months intervals for 2 years with a primary end point of mean reduction in corticosteroid dosage at the 12 month follow-up visit.

NCT ID: NCT01717170 Active, not recruiting - Posterior Uveitis Clinical Trials

Study of the Safety, Tolerability, and Bioactivity of Tocilizumab On Patients With Non-infectious UVEITIS: The STOP-UVEITIS Study

STOP-Uveitis
Start date: March 2013
Phase: Phase 1/Phase 2
Study type: Interventional

In the STOP-UVEITIS study, we propose to evaluate the safety, tolerability, and bioactivity of two doses of Tocilizumab (4mg/kg and 8mg/kg), administered monthly, in patients with non-infectious intermediate, posterior, or panuveitis.

NCT ID: NCT00348153 Active, not recruiting - Uveitis Clinical Trials

Adalimumab in Uveitis Refractory to Conventional Therapy (ADUR Trial)

Start date: August 2006
Phase: Phase 2/Phase 3
Study type: Interventional

TNF alpha Inhibitors have been very effective in treating rheumatologic diseases as well as uveitis. Adalimumab is the first member of a new class of TNF antibody compounds developed to contain exclusively human sequences. We want to test the efficacy and safety of the TNF alpha Inhibitor Adalimumab in patients with active uveitis despite standard immunosuppressive therapy.