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Pemphigus clinical trials

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NCT ID: NCT01559155 Terminated - Pemphigus Clinical Trials

Role of Proteasomes in a Dermatological Autoimmune Disease: Bullous Pemphigoid

Start date: November 5, 2013
Phase:
Study type: Observational

The primary objective of this study is to describe and compare plasmatic anti-proteasome auto-antibody concentrations among three distinct groups: (1) patients suffering from bullous pemphigoide; (2) patients suffering from other dermatological auto-immune diseases; (3) an elderly control group.

NCT ID: NCT01338103 Recruiting - Pemphigus Clinical Trials

Treatment of Pemphigus Patients With Rituximab 1000mgX2 and Assessment of Immune Status Via Cylex

Start date: January 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether Rituximab, in the same doses as used in rheumatoid arthritis patients, will benefit pemphigus patients. It also tests immune function via the Cylex assay in pemphigus patients before and after treatment with RItuximab.

NCT ID: NCT01313923 Recruiting - Pemphigus Clinical Trials

Evaluating Sirolimus to Treat Autoimmune Blistering Dermatosis Pemphigus

Start date: February 2011
Phase: Phase 0
Study type: Interventional

The purpose of this research is to study alternative treatments for the skin disease pemphigus (a rare autoimmune blistering disorder of the skin) by using sirolimus, an immunosuppressive drug. Immunosuppressive drugs inhibit or prevent the activity of the immune system and are commonly used to treat autoimmune diseases, inflammatory diseases, and organ transplantation rejection.

NCT ID: NCT01299857 Completed - Pemphigus Clinical Trials

Long-term Clinical and Biological Evaluation of Patients With Severe Forms of Pemphigus Treated by Rituximab

Suiviritux
Start date: June 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to study the midterm clinical evaluation, biological parameters and immune reconstitution after Rituximab treatment for Pemphigus.

NCT ID: NCT00960713 Completed - Pemphigus Clinical Trials

The RITAI Cohort: An Observational Study on Rituximab Off-label Use for Auto-immune Disorders

RITAI
Start date: June 2009
Phase: N/A
Study type: Observational

The primary purpose of the study is to describe by a prospective observational study the serious adverse events occurring in patients treated off-label by rituximab for various auto-immune diseases.

NCT ID: NCT00784589 Completed - Pemphigus Disease Clinical Trials

Comparison Between Rituximab Treatment and General Corticotherapy Treatment in Patients With Pemphigus

Rituximab 3
Start date: July 2009
Phase: Phase 3
Study type: Interventional

Pemphigus is a severe and sometimes life-threatening disease with a mortality rate between 5 and 10 percent depending on the severity of disease and age of patients. The standard of care is high doses of corticosteroids (CS) (usually, prednisone, 1 to 1.5. mg/kg/day, which are often associated with immunosuppressive drugs i.e., azathioprine, mycophenolate mofetil, cyclophosphamide, cyclosporine, although only one randomised study has demonstrated the superiority of the combination of corticosteroids and immunosuppressive drugs as compared to corticosteroids alone (9). Because of the low frequency of the disease, control trials are difficult to conduct. Evaluation of the different treatment regimens proposed, i;e; corticosteroids alone, CS and immunosuppressive drugs, IV immunoglobulins or new therapeutic regimens such as rituximab (an anti-CD20 monoclonal antibody directed against B- lymphocytes) or immunoadsorbtion.

NCT ID: NCT00683930 Completed - Clinical trials for Pemphigus Vulgaris (PV)

A Study to Assess the Effect of CellCept (Mycophenolate Mofetil) and Reduced Corticosteroids in Patients With Active Pemphigus Vulgaris (PV)

Start date: May 2004
Phase: Phase 3
Study type: Interventional

This study was designed to assess the efficacy and safety of CellCept (1 g or 1.5 g orally twice daily for 52 weeks) in patients with pemphigus vulgaris receiving prednisone or other corticosteroids. During the study, patients had their corticosteroid dose gradually reduced if they responded to treatment. The anticipated time on study treatment was 12 months, and the target sample size was <100 individuals.

NCT ID: NCT00656656 Active, not recruiting - Pemphigus Clinical Trials

Immunoadsorption, Dexamethasone Pulse Therapy and Rituximab for Pemphigus

Start date: January 2008
Phase: Phase 2
Study type: Interventional

Pemphigus is a severe autoimmune blistering disease mediated by circulating antibodies against certain proteins important for maintaining skin integrity. Protein A immunoadsorption is a dialysis-like technique selectively removing the antibodies from patient's blood. Rituximab is a synthetic antibody capable of destroying B cells. B cells are responsible for production of antibodies in the patients blood that, in turn, lead to clinical signs of pemphigus. Dexamethasone pulse therapy is a high-dose short-term corticosteroid therapy that may be used to suppress autoantibody production in pemphigus. While each of these three therapies had been used to treat pemphigus, none was shown effective in all cases. The hypothesis of this study is that a combination of protein A immunoadsorption, rituximab and dexamethasone is more effective that either of these treatments alone in achieving a rapid and durable improvement or cure in patients with pemphigus.

NCT ID: NCT00626678 Completed - Pemphigus Vulgaris Clinical Trials

Azathioprine Versus Placebo in Pemphigus Vulgaris Treated With Prednisolone

Start date: January 2008
Phase: Phase 2
Study type: Interventional

Description: Pemphigus vulgaris is an autoimmune, chronic and recurrent blistering disease with unknown etiology that affects mucosa and skin of patients with significant morbidity and mortality. The treatment back-bone is based on prednisolone administration. There are controversies on the opportunity of adding immunosuppressive drugs. For some, they are just corticosteroid sparing drugs. For others, they are disease modifying drugs. The purpose of this trial is to compare efficacy and safety of azathioprine vs. placebo in new cases of pemphigus vulgaris treated with prednisolone.

NCT ID: NCT00606749 Completed - Pemphigus Vulgaris Clinical Trials

Use of KC706 for the Treatment of Pemphigus Vulgaris

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

The purpose of this study is to determine whether KC706 is effective in the prevention and healing of blisters in patients with pemphigus vulgaris, while the patient remains on stable doses of corticosteroids and/or immunosuppressants.