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Tacrolimus for the Treatment of Systemic Lupus Erythematosus With Membranous Nephritis

Primary Purpose

Lupus Nephritis, Lupus Erythematosus, Systemic

Status
Completed
Phase
Phase 4
Locations
Hong Kong
Study Type
Interventional
Intervention
tacrolimus
Sponsored by
Chinese University of Hong Kong
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Lupus Nephritis focused on measuring SLE, glomerulonephritis, immunosuppressive therapy, type V (membranous) lupus nephritis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Fulfill the revised American College of Rheumatology criteria for SLE Have biopsy-proven membranous nephropathy secondary to SLE Nephrotic syndrome with proteinuria (> 3 g/day) and serum albumin < 30 g/dl, with or without active urinary sediments despite steroid therapy (with or without cytotoxic agents) Age over 18 with informed consent Female patients of child-bearing age and male patients who agree to maintain effective birth control practice during the study Exclusion Criteria: Patient with abnormal liver function tests Patient with hepatitis B surface antigen or who is hepatitis C antibody positive Patient who is diabetic Patient who is receiving non-steroidal anti-inflammatory drugs (NSAIDs) or other agents known to influence urinary protein excretion Patient is allergic or intolerant to macrolide antibiotics or tacrolimus

Sites / Locations

  • Department of Medicine & Therapeutics, Prince of Wales Hospital

Outcomes

Primary Outcome Measures

Change in 24-hour urinary protein excretion

Secondary Outcome Measures

Development of renal flare
Development of non-renal flare

Full Information

First Posted
July 29, 2005
Last Updated
July 31, 2015
Sponsor
Chinese University of Hong Kong
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1. Study Identification

Unique Protocol Identification Number
NCT00125307
Brief Title
Tacrolimus for the Treatment of Systemic Lupus Erythematosus With Membranous Nephritis
Official Title
Tacrolimus for the Treatment of Systemic Lupus Erythematosus With Membranous Nephritis
Study Type
Interventional

2. Study Status

Record Verification Date
May 2008
Overall Recruitment Status
Completed
Study Start Date
January 2004 (undefined)
Primary Completion Date
October 2007 (Actual)
Study Completion Date
February 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Chinese University of Hong Kong

4. Oversight

5. Study Description

Brief Summary
The investigators study the efficacy and safety of tacrolimus in the treatment of membranous nephritis secondary to systemic lupus erythematosus.
Detailed Description
Glomerulonephritis is one of the major disease manifestations of systemic lupus erythematosus (SLE). The treatment of membranous (type V) lupus nephritis, a subset that carries a high morbidity, remains unsatisfactory. Recent studies suggest that immunosuppressive therapy targeted against the calcineurin pathway of T-helper cells, for example, tacrolimus, may be effective in the treatment of primary membranous nephropathy. The investigators plan to conduct an open-label single-arm study of the efficacy and safety of tacrolimus in the treatment of membranous nephropathy secondary to SLE. Twenty patients with biopsy-proven membranous nephropathy secondary to SLE will be recruited. They will be treated with oral prednisolone and tacrolimus for 6 months, followed by 6 months of maintenance steroids alone. Proteinuria, renal function, clinical and serologic lupus activity will be monitored. Complete remission is defined as 24-hour urinary protein excretion to less than 0.5 gm/day. This study will explore the potential role of tacrolimus in the treatment of membranous lupus nephritis, which is usually resistant to conventional therapy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lupus Nephritis, Lupus Erythematosus, Systemic
Keywords
SLE, glomerulonephritis, immunosuppressive therapy, type V (membranous) lupus nephritis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
20 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
tacrolimus
Primary Outcome Measure Information:
Title
Change in 24-hour urinary protein excretion
Secondary Outcome Measure Information:
Title
Development of renal flare
Title
Development of non-renal flare

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Fulfill the revised American College of Rheumatology criteria for SLE Have biopsy-proven membranous nephropathy secondary to SLE Nephrotic syndrome with proteinuria (> 3 g/day) and serum albumin < 30 g/dl, with or without active urinary sediments despite steroid therapy (with or without cytotoxic agents) Age over 18 with informed consent Female patients of child-bearing age and male patients who agree to maintain effective birth control practice during the study Exclusion Criteria: Patient with abnormal liver function tests Patient with hepatitis B surface antigen or who is hepatitis C antibody positive Patient who is diabetic Patient who is receiving non-steroidal anti-inflammatory drugs (NSAIDs) or other agents known to influence urinary protein excretion Patient is allergic or intolerant to macrolide antibiotics or tacrolimus
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cheuk-Chun Szeto, MD
Organizational Affiliation
Chinese University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Medicine & Therapeutics, Prince of Wales Hospital
City
Shatin
Country
Hong Kong

12. IPD Sharing Statement

Learn more about this trial

Tacrolimus for the Treatment of Systemic Lupus Erythematosus With Membranous Nephritis

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