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Lupus Nephritis clinical trials

View clinical trials related to Lupus Nephritis.

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NCT ID: NCT00881309 Completed - Lupus Nephritis Clinical Trials

To Compare the Efficacy and Safety of Tripterygium (TW) Versus AZA in the Maintenance Therapy for Lupus Nephritis

Start date: March 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to: - To access the efficacy of TW compared to Aza in the maintenance therapy for lupus nephritis - To investigate the safety and tolerability of TW versus Aza in the maintenance therapy for lupus nephritis

NCT ID: NCT00876616 Completed - Lupus Nephritis Clinical Trials

Assess the Efficacy and Safety of Multi-target Therapy in Lupus Nephritis

Start date: April 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the efficacy and safety of multi-target therapy in the treatment of class Ⅲ,Ⅳ,Ⅴ,Ⅲ+Ⅴand Ⅳ+Ⅴ lupus nephritis.

NCT ID: NCT00774852 Completed - Lupus Nephritis Clinical Trials

Abatacept and Cyclophosphamide Combination Therapy for Lupus Nephritis

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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: NCT00709722 Completed - Lupus Nephritis Clinical Trials

Safety and Efficacy on Deoxyspergualin (NKT-01) in Patients With Lupus Nephritis

Start date: October 2003
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of the open multi-center study is to determine an efficient and safe dose and dosing schedule of NKT-01 in induction of response in treatment of lupus nephritis.

NCT ID: NCT00705367 Completed - Lupus Nephritis Clinical Trials

Phase I Study in China - Tolerability of a Single Dose of Abatacept 30 mg/kg

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

The purpose of this study is to determine whether abatacept at a dose 30 mg/kg via intravenous infusion is safe and well tolerated in the treatment of lupus nephritis in mainland Chinese subjects with systemic lupus erythematosus (SLE)

NCT ID: NCT00615173 Completed - Kidney Diseases Clinical Trials

Prospective, Randomized, Multicenter, Control Study to Assess the Efficacy and Safety of Tacrolimus in Induction and Maintenance Phase Treatment in Lupus Nephritis

Start date: July 2006
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the efficacy and safety of tacrolimus vs intravenous cyclophosphamide pulses treatment for the induction therapy of LN(III,IV,V). To compare the efficacy and safety of tacrolimus vs Azathioprine for the maintenance therapy of LN(III,IV,V).

NCT ID: NCT00429377 Completed - Lupus Nephritis Clinical Trials

Phase 3 Study of Tacrolimus (FK506) for Lupus Nephritis: A Placebo Controlled, Double-Blind Multicenter, Comparative Study

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

This study consists of a 28-week placebo-controlled double-blind inter-group efficacy study in steroid refractory Lupus Nephritis patients.

NCT ID: NCT00423098 Completed - Lupus Nephritis Clinical Trials

Efficacy and Safety of Enteric-coated Mycophenolate Sodium in Combination With Two Corticosteroid Regimens for the Treatment of Lupus Nephritis Flare

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

The study will investigate the efficacy and safety of enteric-coated mycophenolate sodium in combination with two different corticosteroid (CS) regimes for the induction of remission of a lupus nephritis flare. Patients will be randomly allocated to standard CS regimen (group I) or to a reduced dose CS regimen (group II)

NCT ID: NCT00404794 Completed - Lupus Nephritis Clinical Trials

A Study to Compare Mycophenolate Mofetil and Tacrolimus in the Treatment of Membranous Lupus Nephritis

Start date: November 2005
Phase: Phase 3
Study type: Interventional

This is a prospective randomized open-label pilot study to compare mycophenolate mofetil in combination with corticosteroid treatment and tacrolimus in combination with corticosteroid treatment in membranous lupus nephritis. The change in urine protein excretion will be the primary outcome studied. The study duration will be 24 months for each patient.

NCT ID: NCT00377637 Completed - Lupus Nephritis Clinical Trials

A Study of Mycophenolate Mofetil (CellCept) in Management of Patients With Lupus Nephritis.

Start date: July 2005
Phase: Phase 3
Study type: Interventional

This 2 arm study assessed the efficacy of Mycophenolate Mofetil (MMF; CellCept) compared to cyclophosphamide in inducing a response in patients with lupus nephritis, and the long term efficacy of MMF compared to azathioprine in maintaining remission and renal function. Patients were randomized to receive either MMF (1.5 g twice daily [bid]) or cyclophosphamide (0.5-1.0 g/m^2 in monthly pulses) in the induction phase. Those patients meeting criteria for response were re-randomized for entry into the maintenance phase, to receive either MMF (1 g bid) or azathioprine (2 mg/kg/day).