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Lupus Erythematosus, Systemic clinical trials

View clinical trials related to Lupus Erythematosus, Systemic.

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NCT ID: NCT00911521 Completed - Clinical trials for Systemic Lupus Erythematosus

Immunogenicity and Safety of a Quadrivalent Human Papillomavirus (HPV) Vaccine in Patients With SLE: a Controlled Study

Start date: October 2009
Phase: Phase 4
Study type: Interventional

The purpose of this trial is to study the effect of Human Papillomavirus (HPV) vaccination on the elevation of antibody titer to 4 serotypes of HPV in patients with systemic lupus erythematous and compare the antibody response with an equal number of age-matched healthy women.

NCT ID: NCT00828178 Completed - Clinical trials for Systemic Lupus Erythematosus

Efficacy of Fish Oil in Lupus Patients

Start date: February 2009
Phase: Phase 4
Study type: Interventional

The investigators hypothesize that low-dose dietary supplementation with omega-3 fish oil will improve disease activity and endothelial function in Systemic Lupus Erythematosus (SLE) patients.

NCT ID: NCT00818948 Completed - Clinical trials for Systemic Lupus Erythematosus

Safety Study of AMG 811 in Subjects With Systemic Lupus Erythematosus With and Without Glomerulonephritis

Start date: March 2009
Phase: Phase 1
Study type: Interventional

This is a 2-part, multi-center, randomized, double-blind, placebo-controlled, multiple dose escalation study, enrolling approximately 48 subjects. Part A of the study will enroll subjects with Systemic Lupus Erythematosus (SLE) without Glomerulonephritis (GN) into 3 cohorts. Part B of the study will enroll SLE subjects with GN into 3 cohorts. The purpose of the study is to evaluate the multiple dose of AMG 811 on safety. Tolerability and pharmacokinetics.

NCT ID: NCT00815282 Completed - Clinical trials for Systemic Lupus Erythematosus

Immune Response After Human Papillomavirus Vaccination in Patients With Autoimmune Disease

HPV-kind
Start date: February 2009
Phase: Phase 4
Study type: Interventional

In the Netherlands, the human Papillomavirus (HPV) vaccination will be added to the National Vaccination Program for girls to protect against the development of cervical cancer. The vaccine protects against HPV type 16 & 18, which cause about 75% of cervical cancer. Studies have shown that the vaccine is effective in healthy subjects in preventing infection by HPV 16 & 18. However, no evidence exists on the immunogenicity and safety of HPV vaccination in patients with an immune system disorder, such as primary humoral immunodeficiency (i.e. hypogammaglobulinemia) or autoimmune diseases. Concerns exist that vaccination may cause an aggravation of the underlying disease. In addition, the immune response to vaccination may be diminished due to immunosuppressive therapy or the underlying disease. Objective: The primary goal of the current study is to study the immunogenicity of HPV vaccination in patients with an autoimmune disease and a primary humoral immunodeficiency. Based on retrospective analysis with other vaccines we hypothesize that patients with autoimmune diseases who are under immunosuppressive medication and patients with a immune system disorder have a decreased serological response to HPV vaccination, and that the produced HPV antibodies titers decrease more rapidly than in healthy individuals. The secondary objective is to explore safety of HPV vaccination and immune regulatory mechanisms induced by vaccination in a subset of patients. The investigators hypothesize that HPV vaccination is safe and that HPV-induced regulatory T cells are able to prevent an increase in the activity of an autoimmune disease.

NCT ID: NCT00786409 Completed - Clinical trials for Systemic Lupus Erythematosus

Immunogenicity and Safety of HPV Vaccine Gardasil in Young Women

Start date: November 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the immunogenicity and safety of the HPV vaccine Gardasil in young women.

NCT ID: NCT00779194 Completed - Clinical trials for Systemic Lupus Erythematosus (SLE)

Prospective Study of Rapamycin for the Treatment of SLE

Rapamune
Start date: October 2008
Phase: Phase 2
Study type: Interventional

Systemic lupus erythematosus (SLE) is an autoimmune disease of unknown origin. It involves multiple organs including the joints, skin, kidneys and central nervous system. The disease process is caused by a dysfunction of the immune system. The drugs currently used for the treatment of SLE are only partially effective and carry significant risks for side-effects. Patients that were resistant or intolerant to conventional medication have been effectively treated with Rapamycin and were able to decrease the amount of prednisone they needed. The purpose of this study is to prospectively determine the therapeutic efficacy and mechanism of action of Rapamune in patients with SLE. Healthy subjects not receiving Rapamune will be asked to donate blood to serve as controls only for immunobiological outcomes. As part of the research effort to understand the reason for the variations in the effects of treatment drugs by different individuals, a sub-study of the DNA makeup of subjects enrolled in the trial will also be done. The purpose of the sub-study is to possibly determine whether different responses to the drugs used to treat SLE have a correlation with the differences in the genetic makeup of the subjects.

NCT ID: NCT00774943 Completed - Clinical trials for Systemic Lupus Erythematosus

A Study of AMG 557 in Adults With Systemic Lupus Erythematosus

Start date: December 2008
Phase: Phase 1
Study type: Interventional

This is a Phase 1, randomized, placebo-controlled, double-blind, dose-escalation study of repeat SC doses of AMG 557 in adults with Systemic Lupus Erythematosus.

NCT ID: NCT00774852 Completed - Lupus Nephritis Clinical Trials

Abatacept and Cyclophosphamide Combination Therapy for Lupus Nephritis

ACCESS
Start date: November 2008
Phase: Phase 2
Study type: Interventional

This study is for individuals with lupus who have developed complications in their kidneys, or lupus nephritis. The study will determine whether adding the experimental medication abatacept to standard cyclophosphamide therapy is more effective in improving lupus nephritis than standard cyclophosphamide therapy by itself.

NCT ID: NCT00731302 Completed - Clinical trials for Systemic Lupus Erythematosus

Aspirin Resistance in Systemic Lupus Erythematosus (SLE)

Start date: April 2005
Phase: Phase 1
Study type: Interventional

This study examine whether patients with lupus respond to aspirin , and if not, if that is related to inflammation. We examine the ability of aspirin to inhibit the production of thromboxane in patients with lupus and controls and see if aspirin insensitive thromboxane production is inhibited by meloxicam.

NCT ID: NCT00730002 Completed - Clinical trials for Neuropsychiatric Systemic Lupus Erythematosus

Magnetic Resonance Spectroscopy, Perfusion, and Diffusion Tensor Imaging in Neuropsychiatric Lupus

Start date: March 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if three functional Magnetic Resonance brain imaging techniques: Magnetic Resonance Spectroscopy(MRS),Magnetic Resonance perfusion, and Diffusion Tensor Imaging(DTI) can detect brain alterations distinctive for neuropsychiatric systemic lupus erythematosus (NPSLE)and systemic lupus erythematosus(SLE).