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Pemphigus clinical trials

View clinical trials related to Pemphigus.

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NCT ID: NCT00483119 Terminated - Pemphigus Vulgaris Clinical Trials

Randomized Trial of IVIg With or Without Cyclophosphamide in Pemphigus

Start date: April 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to compare two standard treatments for pemphigus to determine which more effectively improves the clinical manifestations of the disease and decreases serum level of the autoantibodies which cause the disease.

NCT ID: NCT00429533 Terminated - Pemphigus Vulgaris Clinical Trials

Efficacy of Dapsone as a Steroid Sparing Agent in Pemphigus Vulgaris

Start date: November 1996
Phase: Phase 2
Study type: Interventional

The purpose of this 12-month study was to determine the efficacy of dapsone as a glucocorticoid-sparing agent in maintenance phase pemphigus vulgaris.

NCT ID: NCT00283712 Completed - Pemphigus Clinical Trials

Use of Infliximab for the Treatment of Pemphigus Vulgaris

Start date: March 2006
Phase: Phase 2
Study type: Interventional

Pemphigus vulgaris (PV) is a rare skin disorder that causes blistering of the skin and mucous membranes. Infliximab is a man-made antibody used to treat certain types of immune system disorders, including rheumatoid arthritis and Crohn's disease. This study will determine if infliximab given in combination with prednisone is a safe and effective treatment for adults with PV.

NCT ID: NCT00278642 Terminated - Pemphigus Clinical Trials

Hematopoietic Stem Cell Support in Patients With Autoimmune Bullous Skin Disorders

Start date: September 2002
Phase: Phase 1
Study type: Interventional

Autoimmune Bullous Skin Disorders are believed to be due to immune cells, cells that normally protect the body and are now causing damage to the body. This study is designed to examine whether treating patients with high dose cyclophosphamide (a drug which reduces the function of the immune system) together with anti-thymocyte globulin (a protein that kills the immune cells that are thought to be causing your disease), followed by return of the previously collected special blood cells (stem cells) will result in improvement of this disease. Stem cells are undeveloped cells that have the capacity to grow into mature blood cells, which normally circulate in the blood stream. The purpose of the intense chemotherapy is to destroy the cells in the immune system which may be causing this skin disease. The purpose of the stem cell infusion is to restore the body's blood production, which will be severely impaired by the high dose chemotherapy and anti-thymocyte globulin.

NCT ID: NCT00213512 Completed - Pemphigus Clinical Trials

Effect of Anti CD20 in Pemphigus Desease

Start date: June 2003
Phase: Phase 2/Phase 3
Study type: Interventional

to treat in an open non comparative clinical study patients presenting pemphigus with corticodependance, corticoresistance and contre-indication to systemic steroids.

NCT ID: NCT00135720 Completed - Pemphigus Vulgaris Clinical Trials

Study of Etanercept (Enbrel) in the Treatment of Pemphigus Vulgaris

Start date: June 2004
Phase: Phase 2
Study type: Interventional

The purpose of the study is to find out about the effectiveness and the safety of an investigational drug called etanercept (Enbrel) to treat pemphigus vulgaris. Pemphigus vulgaris is a potentially life threatening blistering condition that currently has no cure. An investigational drug is one that has not been approved by the United States (US) Food and Drug Administration (FDA) to treat a particular condition or disease. Etanercept has been approved by the FDA to treat rheumatoid arthritis, juvenile rheumatoid arthritis, and psoriasis, but not pemphigus vulgaris.

NCT ID: NCT00127764 Completed - Pemphigus Clinical Trials

European Trial of Adjuvant Oral Glucocorticoid Pulse Therapy in Pemphigus

Start date: January 2001
Phase: Phase 2/Phase 3
Study type: Interventional

By this study, the investigators want to test if the value of adjuvant pulse glucocorticoid therapy for pemphigus can be determined by comparing an experimental arm (dexamethasone pulse therapy, prednisolone, and azathioprine) with a control arm (placebo pulse therapy, prednisolone, and azathioprine). The investigators will determine the rate of complete remission with dexamethasone pulse therapy; the time needed for complete remission; and the duration of remission, and compare these data with those of the placebo arm.

NCT ID: NCT00063752 Completed - Pemphigus Vulgaris Clinical Trials

Safety Study of PI-0824 to Treat Pemphigus Vulgaris

Start date: July 2003
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine if the use of PI-0824 in patients with Pemphigus vulgaris is safe.

NCT ID: NCT00010413 Completed - Pemphigus Clinical Trials

Phase II Study of High-Dose Cyclophosphamide in Patients With Refractory Pemphigus

Start date: April 1999
Phase: Phase 2
Study type: Interventional

OBJECTIVES: I. Determine the response rate and 1-year event-free survival of patients with refractory pemphigus treated with high-dose cyclophosphamide.