Long-Acting Tacrolimus for the Treatment of Resistant Lupus Nephritis
Primary Purpose
Lupus Nephritis
Status
Completed
Phase
Phase 4
Locations
Hong Kong
Study Type
Interventional
Intervention
Long-acting tacrolimus (Advagraf, Astellas Pharma)
Sponsored by
About this trial
This is an interventional treatment trial for Lupus Nephritis focused on measuring glomerulonephritis, systemic lupus erythematosus
Eligibility Criteria
Inclusion Criteria:
- Age over 18 with informed consent.
- Fulfill the revised American College of Rheumatology criteria for SLE
- Biopsy-proven class III, IV, or V lupus nephritis within the past 24 months.
- Could not achieve complete remission after at least 4 months of conventional therapy (oral steroid plus cyclosphosphamide or mycophenolate mofetil).
- NB. Complete response is defined as proteinuria less than 0.5 g/day, with normal urinary sediment, a normal serum albumin concentration, and serum creatinine <15% above the base-line value.
- Female patients of child-bearing age and male patients agree to maintain effective birth control practice during the study.
Exclusion Criteria:
- Abnormal liver function tests
- Hepatitis B surface antigen or hepatitis C antibody positive
- Diabetic
- Receiving NSAID or other agents known to influence urinary
- Protein excretion
- Allergic or intolerant to macrolide antibiotics or tacrolimus
Sites / Locations
- Prince of Wales Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
advagraf
Arm Description
Long-acting tacrolimus (Advagraf, Astellas Pharma) will be started at single daily dose of 0.15-0.2 mg/kg/day for 6 months.
Outcomes
Primary Outcome Measures
overall clinical response
complete response is defined as urinary protein < 0.5 g/day, with normal urinary sediment, normal serum albumin, and serum creatinine < 15% above the base-line value. Partial response is defined as urinary protein between 0.6 and 2.9 g/day, with a serum albumin > 30 g/dL, and stable renal function. No response is defined as urinary protein > 3 g/day or a value of 0.6 to 2.9 g/day but serum albumin < 30 g/dL, an increase in serum creatinine ≥ 50 µmol/l or 15% above the base-line value, or the discontinuation of treatment due to side effects.
Secondary Outcome Measures
change in SLEDAI score
24-hour urinary protein excretion
renal function
development of lupus flare (renal or non-renal)
Full Information
NCT ID
NCT01206569
First Posted
September 21, 2010
Last Updated
December 3, 2012
Sponsor
Chinese University of Hong Kong
1. Study Identification
Unique Protocol Identification Number
NCT01206569
Brief Title
Long-Acting Tacrolimus for the Treatment of Resistant Lupus Nephritis
Official Title
Long-Acting Tacrolimus for the Treatment of Resistant Lupus Nephritis
Study Type
Interventional
2. Study Status
Record Verification Date
December 2012
Overall Recruitment Status
Completed
Study Start Date
September 2010 (undefined)
Primary Completion Date
December 2011 (Actual)
Study Completion Date
February 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Glomerulonephritis is one of the major disease manifestations of systemic lupus erythematosus (SLE). Around one-third of the patients, however, do not respond to conventional immunosuppressive therapy, and they have a high risk of progressing to dialysis-dependent renal failure. Recent studies suggest that immunosuppressive therapy targeted against the calcineurin pathway of T-helper cell, for example, tacrolimus, may be effective in the treatment of primary glomerulonephritis. The investigators plan to an open-label single-arm study the efficacy and safety of long-acting tacrolimus in the treatment of treatment-resistant lupus nephritis. Twenty-five patients with biopsy-proven lupus nephritis will be recruited. They will be treated with oral prednisolone and long-acting tacrolimus for 6 months, followed by 6 months of maintenance steroid and azathioprine. Proteinuria, renal function, clinical and serologic lupus activity will be monitored. This study will explore the potential role of long-acting tacrolimus in resistant lupus nephritis, which has a poor prognosis and no effective treatment at the moment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lupus Nephritis
Keywords
glomerulonephritis, systemic lupus erythematosus
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
2 (Actual)
8. Arms, Groups, and Interventions
Arm Title
advagraf
Arm Type
Experimental
Arm Description
Long-acting tacrolimus (Advagraf, Astellas Pharma) will be started at single daily dose of 0.15-0.2 mg/kg/day for 6 months.
Intervention Type
Drug
Intervention Name(s)
Long-acting tacrolimus (Advagraf, Astellas Pharma)
Intervention Description
Long-acting tacrolimus (Advagraf, Astellas Pharma) will be started at single daily dose of 0.15-0.2 mg/kg/day for 6 months.
Primary Outcome Measure Information:
Title
overall clinical response
Description
complete response is defined as urinary protein < 0.5 g/day, with normal urinary sediment, normal serum albumin, and serum creatinine < 15% above the base-line value. Partial response is defined as urinary protein between 0.6 and 2.9 g/day, with a serum albumin > 30 g/dL, and stable renal function. No response is defined as urinary protein > 3 g/day or a value of 0.6 to 2.9 g/day but serum albumin < 30 g/dL, an increase in serum creatinine ≥ 50 µmol/l or 15% above the base-line value, or the discontinuation of treatment due to side effects.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
change in SLEDAI score
Time Frame
6 months
Title
24-hour urinary protein excretion
Time Frame
6 months
Title
renal function
Time Frame
6 months
Title
development of lupus flare (renal or non-renal)
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age over 18 with informed consent.
Fulfill the revised American College of Rheumatology criteria for SLE
Biopsy-proven class III, IV, or V lupus nephritis within the past 24 months.
Could not achieve complete remission after at least 4 months of conventional therapy (oral steroid plus cyclosphosphamide or mycophenolate mofetil).
NB. Complete response is defined as proteinuria less than 0.5 g/day, with normal urinary sediment, a normal serum albumin concentration, and serum creatinine <15% above the base-line value.
Female patients of child-bearing age and male patients agree to maintain effective birth control practice during the study.
Exclusion Criteria:
Abnormal liver function tests
Hepatitis B surface antigen or hepatitis C antibody positive
Diabetic
Receiving NSAID or other agents known to influence urinary
Protein excretion
Allergic or intolerant to macrolide antibiotics or tacrolimus
Facility Information:
Facility Name
Prince of Wales Hospital
City
Shatin
Country
Hong Kong
12. IPD Sharing Statement
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Long-Acting Tacrolimus for the Treatment of Resistant Lupus Nephritis
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