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Uveitis clinical trials

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NCT ID: NCT02907814 Terminated - Uveitis Clinical Trials

Measurement of Anterior Chamber Cell Grading Using Ocular Coherence Tomography

Start date: September 2016
Phase: N/A
Study type: Interventional

Optical Coherence Tomography (OCT) is routinely used in ophthalmic clinical practice. It uses infrared light to image patient's eyes. Some patients, such as those with an inflammatory disease called uveitis or those who have just undergone cataract surgery, have intraocular inflammation. This intraocular inflammation commonly manifests as cells that can be seen on routine microscopic clinical examination. However, the only currently available method to quantify this intraocular inflammation is by manually counting on the microscopic clinical examination. The investigators plan to use the OCT machine to image patient's eyes. The investigators will then use the images obtained from the OCT to objectively quantify the degree of intraocular inflammation.

NCT ID: NCT02769702 Terminated - Uveitis Clinical Trials

Open Label Study of Acthar SQ Gel Injection in Patients With Active Anterior Uveitis

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

Uveitis is an acute or chronic inflammatory condition of unknown etiology. Although uveitis often responds adequately to topical corticosteroids, there are many patients for which this treatment is either inadequate or not tolerated. A patient with inadequate response to treatment would manifest uveitis activity by slit lamp examination determination of anterior chamber cellularity. Lack of tolerance of therapy commonly manifests as ocular hypertension (greater than 21 mmHg measured by tonometry)complicating chronic topical corticosteroid administration, leading to glaucoma and permanent visual loss. Moreover, systemic corticosteroids may be required at a dose unsafe for chronic administration. In these situations, an immunosuppressive medication is often added as a "steroid-sparing" agent. If and when there is clinical response to the added immunosuppressive, the oral and/or topical corticosteroid dose can be reduced or eliminated to avoid toxicity. There are several reasons for believing that Acthar might be beneficial in the treatment of uveitis patients. In addition to increasing adrenal production or cortisol, Acthar has another important mechanisms of action mediated by its binding of melanocortin receptors. Melanocortin down-regulates activity of B and T lymphocytes, monocytes and macrophages. In animal studies, melanocortin peptides down-regulate T helper cells, up-regulate T Regulatory cells, and decrease B lymphocyte production of B Lymphocyte Stimulator. In macrophages, there is down-regulation of IL-1, IL-2, INF gamma, TNF alpha, nitric oxide and adhesion molecules. In other cells, in addition to IL-10 upregulation (monocytes), there is down-regulation of VACM and ECAM (endothelial cells), prostaglandins (fibroblasts) and MCP-1 and RANTES (renal tubules).CNS mediation of systemic inflammation may also be down-regulated by melanocortin receptor binding by Acthar.

NCT ID: NCT02375685 Terminated - Chronic Uveitis Clinical Trials

Long-term Safety of Gevokizumab in the Treatment of Patients With Chronic Non-infectious Uveitis (EYEGUARD-X)

EYEGUARD-X
Start date: August 2014
Phase: Phase 3
Study type: Interventional

The objective of this study is to evaluate long-term safety of gevokizumab in patient with chronic non-infectious uveitis who previously well tolerated the study drug and may benefit from longterm treatment with gevokizumab.

NCT ID: NCT02258867 Terminated - Clinical trials for Behcet's Disease Uveitis

Efficacy and Safety Study of Gevokizumab to Treat Behcet's Disease Uveitis

EYEGUARD™-US
Start date: November 2014
Phase: Phase 3
Study type: Interventional

The objective of this study is to assess the efficacy and safety of gevokizumab in treating Behcet's disease uveitis (BDU).

NCT ID: NCT02258854 Terminated - Uveitis Clinical Trials

An Open-label, Rollover Study Providing Continued Dosing of Gevokizumab in Order to Assess Long-term Gevokizumab Safety Data

EYEGUARD™-E
Start date: March 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to provide continued dosing of gevokizumab in order to obtain and assess long-term gevokizumab safety data.

NCT ID: NCT02131012 Terminated - Inflammation Clinical Trials

Intravitreal Celecoxib for Chronic Uveitis

Celecoxib
Start date: June 2015
Phase: Phase 1
Study type: Interventional

Intraocular delivery of celecoxib will be an effective means to treat inflammation and macular edema and prevent structural complications and vision loss in patients with chronic inflammation or macular edema who are unable to tolerate corticosteroids due to their side effects.

NCT ID: NCT02125266 Terminated - Uveitis, Posterior Clinical Trials

Safety and Preliminary Efficacy Study of V404 PDS in Uveitis

Start date: April 2014
Phase: Phase 1/Phase 2
Study type: Interventional

This study is intended to evaluate the safety of V404 PDS in patients with chronic non-infectious uveitis. Secondarily, the study will evaluate whether V404 PDS can provide clinically measurable benefit over an extended period of time in patients with chronic non-infectious uveitis.

NCT ID: NCT01965145 Terminated - Behcet's Uveitis Clinical Trials

Efficacy of Gevokizumab in the Treatment of Patients With Behçet's Disease Uveitis (EYEGUARD™-B)

EYEGUARD™-B
Start date: November 2012
Phase: Phase 3
Study type: Interventional

The objective of this study is to demonstrate the superiority of gevokizumab as compared to placebo on top of current standard of care in reducing the risk of Behçet's disease uveitis exacerbations

NCT ID: NCT01939691 Terminated - Macular Edema Clinical Trials

Macular Edema Nepafenac vs. Difluprednate Uveitis Trial

MEND
Start date: September 12, 2018
Phase: Phase 4
Study type: Interventional

Macular edema is a condition in which there is swelling in the macula, the part of the retina that gives you your best vision. This swelling can cause your vision to decline. When diagnosed early and treated, you vision usually can be preserved. However, if the swelling goes untreated for a long time, it can cause permanent vision loss. We think that the three eye drop regimens in this study, difluprednate, difluprednate plus nepafenac, and prednisolone acetate plus nepafenac, might be effective in treating uveitic macular edema. Patients who enter this study are randomized to one of the three regimens and followed for 24 weeks.

NCT ID: NCT01747538 Terminated - Uveitis Clinical Trials

Safety and Efficacy Study of Gevokizumab to Treat Non-infectious Uveitis Controlled With Systemic Treatment

EYEGUARD™-C
Start date: October 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy of gevokizumab in reducing the risk of recurrent uveitic disease in subjects with non-infectious uveitis whose disease is currently controlled with systemic treatment.