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Nephritis clinical trials

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NCT ID: NCT01369628 Terminated - Lupus Nephritis Clinical Trials

Atacicept in Lupus Nephritis Patients Taking Stable Regimen of Mycophenolate Mofetil

Start date: June 2011
Phase: Phase 1
Study type: Interventional

The sponsor electively terminated the study because the risk mitigation measures, deemed necessary after an unforeseen safety event, could not be effectively implemented within this protocol while maintaining study timelines within a reasonable time frame.

NCT ID: NCT01342016 Terminated - Lupus Nephritis Clinical Trials

A Study to Compare the Efficacy and Safety of Tacrolimus Capsules With Leflunomide Tablets in Lupus Nephritis Patients

Start date: April 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the efficacy and safety of tacrolimus capsules with leflunomide tablets in the treatment of lupus nephritis.

NCT ID: NCT01338363 Completed - Pneumonia Clinical Trials

Drug Utilization and Safety Events Among Children Using Esomeprazole, Other Proton Pump Inhibitors or H2-receptor Antagonists

Start date: May 2011
Phase: N/A
Study type: Observational

The purpose of this study is 1. To describe patient characteristics and drug usage among children that are prescribed esomeprazole for the first time and to compare them with patients who are prescribed other proton pump inhibitors (PPIs) or H2-receptor antagonists for the first time. 2. To ascertain all incident hospitalized cases of angioneurotic oedema, pneumonia, gastroenteritis, failure to thrive, convulsions/seizures, acute interstitial nephritis and thrombocytopenia among new users in the three cohorts of esomeprazole, other PPIs and H2-receptor antagonists.

NCT ID: NCT01328834 Completed - Nephritis, Lupus Clinical Trials

Efficacy and Safety of Tacrolimus Sustained-release Capsules in Induction Treatment in Refractory Lupus Nephritis

Start date: January 2011
Phase: Phase 3
Study type: Interventional

This a pilot study to evaluate the efficacy and safety of Tacrolimus Sustained-release Capsules (ADVAGRAF) treatment for the induction therapy of refractory lupus nephritis (LN).

NCT ID: NCT01316133 Terminated - Lupus Nephritis Clinical Trials

A Study to Evaluate the Efficacy and Safety of Tacrolimus With Steroid in Korean Lupus Nephritis Patients

APPLE
Start date: April 19, 2011
Phase: Phase 4
Study type: Interventional

This study is to evaluate efficacy and safety of tacrolimus with steroid by observing remission rate at 24 weeks in lupus nephritis patients who are non-responders to steroid monotherapy.

NCT ID: NCT01312727 Completed - Gout Clinical Trials

Hereditary Tubulointerstitial Nephritis

NTIH
Start date: November 2010
Phase: N/A
Study type: Interventional

The aim of this study is to identify families with hereditary chronic tubulointerstitial renal diseases , characterize the phenotype and screen for mutations in known genesis (UMOD, REN, TCF2, NPHP1). Genome wide analysis will be performed in families without mutations identified.

NCT ID: NCT01299922 Withdrawn - Lupus Nephritis Clinical Trials

Clinical Trial Treatment in Lupus Nephritis

Csa-LES
Start date: February 2011
Phase: Phase 3
Study type: Interventional

The treatment of lupus nephritis with cyclophosphamide and steroids changed the prognosis of lupus nephritis in the early '80s. In recent years, alternative regimens have appeared in both the induction and maintenance with similar results at least to those offered by the classic pattern and possibly with fewer side effects, especially for long term. The association of prednison and mycophenolate has created large expectations to that effect, and is part of first-line therapeutic arsenal of lupus nephritis type III, IV and V. Despite the significant advances that have led to these treatments, the likelihood of complete remission after six months remains, according to the series of 8-13% and partial remission do not exceed 60% in papers published. In the last year, two articles have been published supporting the use of triple therapy (prednisone, mycophenolate, cyclosporine) in poor prognosis of lupus nephritis with hopefully better results than those obtained previously. In this study we try to compare the effectiveness of triple therapy, the therapy is now considered standard (prednisone, mycophenolate) in patients with lupus nephritis type III-IV-V

NCT ID: NCT01288664 Withdrawn - Lupus Nephritis Clinical Trials

Efficacy and Safety of Tacrolimus Sustained-release Capsules in Induction Phase Treatment in Lupus Nephritis

Start date: January 2011
Phase: Phase 3
Study type: Interventional

This is a pilot study to evaluate the efficacy and safety of Tacrolimus Sustained-release Capsules (ADVAGRAF) for the induction therapy of Lupus Nephritis (LN) (V, III +V, IV+V).

NCT ID: NCT01284725 Active, not recruiting - Nephritis of Lupus Clinical Trials

Weaning of Immunosuppression in Nephritis of Lupus

WIN-Lupus
Start date: January 2011
Phase: Phase 3
Study type: Interventional

The investigators wish to evaluate the discontinuation of maintenance immunosuppressive treatment after 2 years in patients with stable remission after a proliferative lupus nephritis. The patients will be continuing their treatment with hydroxychloroquine, possibly associated with low dose corticosteroids.

NCT ID: NCT01273389 Completed - Lupus Nephritis Clinical Trials

An Efficacy and Safety Study of CNTO 136 in Patients With Active Lupus Nephritis

Start date: August 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of CNTO 136 administered intravenously in patients with active, International Society of Nephrology/Renal Pathology Society Class III and IV Lupus Nephritis (LN).