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View Clinical Trial (Medical Research Study)
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Etanercept for the Treatment of Lupus Nephritis - NCT00447265-27709 (Clinical Trial 165568)
Permalink: http://www.ClinicalConnection.com/exp/ExpandedPatientViewStudy165568.aspx
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| City: |
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Durham |
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State:
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NC |
| Zip Code: |
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27709 |
| Conditions: |
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Lupus Nephritis |
| Purpose: |
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Systemic lupus erythematosus (SLE) is a chronic, multisystem, autoimmune disease in which
the body's immune system attacks its own normal tissues. This abnormal autoimmune response
can result in damage to many parts of the body, including the skin, joints, lungs, heart,
brain, intestines, and kidneys. Kidney problems occur in 60-75 % of lupus patients. The
development of lupus-related kidney disease (called lupus nephritis) is associated with an
overall worse prognosis.
SLE is usually treated with drugs that try to block inflammation caused by the immune
system. These treatments can create their own problems and they do not cure lupus. The
drugs that are often used to treat lupus nephritis include prednisone (steroids),
cyclophosphamide (Cytoxan), azathioprine (AZA or Imuran), and mycophenolate mofetil (MMF or
Cellcept). The main purpose of this study is to evaluate the safety and tolerability of
etanercept compared to placebo in combination with standard of care to treat individuals
with active lupus nephritis.
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| Study summary: |
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Kidney problems associated with lupus nephritis range from asymptomatic protein in the urine
to rapidly progressive glomerulonephritis, leading to end-stage renal disease. The goal of
therapies is to control kidney manifestations in order to avoid kidney failure, the
occurrence of other medical problems and death.
The treatment of lupus nephritis remains problematic. Despite the use of currently
available therapies, patients experience disease relapse. Over time, patients develop
significant morbidity from the disease as well as from medications used for treatment.
Etanercept, a TNF inhibitor, is proposed as a potential treatment for lupus nephritis. TNF
increases the number of reactive B and T cells. TNF levels can be elevated in lupus.
Etanercept is believed to work by blocking inflammation, and it is hoped that it will lessen
the signs and symptoms of lupus-related kidney disease.
The purpose of this study is to evaluate the safety and tolerability of etanercept compared
to placebo in combination with standard therapy to treat individuals with mild or moderately
active lupus nephritis.
This study will last 1 year. Participants will be randomly assigned to receive either
etanercept or placebo in addition to their regular medications. Participants will
self-administer 50 mg etanercept or placebo injections once a week. They will continue
receiving their usual treatment with corticosteroids and either MMF, Mycophenolic Acid, or
AZA. Treatment with study medication will occur for 24 weeks.
There will be a screening visit followed by a randomization visit, where subjects will
receive and learn how to administer the study drug. Subjects will come to the clinic for 9
study visits. A physical exam and blood and urine collection will occur at most study
visits. Participants will also be asked to complete a questionnaire on their health at most
study visits. Subjects will be contacted by phone 5 times during the 24-week period to
assess for adverse events and worsening disease status. |
| Criteria: |
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Inclusion Criteria:
- Meets at least 4 of the 11 American College of Rheumatology (ACR) 1982 Revised
Criteria for the Classification of SLE
- Active lupus nephritis
- Currently has antibodies to double-stranded DNA (dsDNA)
- Currently receiving treatment consisting of at least 1.5 g/day of MMF OR at least 720
mg/day orally of Mycophenolic Acid OR at least 1.5 mg/kg once per day of AZA for
lupus nephritis, for at least 28 days prior to study entry
- Stable medication regimen for at least 4 weeks prior to study entry
- Able and willing to self-administer study drug OR has a designated caregiver at home
to administer study drug injections
- Willing to use acceptable forms of contraception for the duration of the study
Exclusion Criteria:
- Moderately severe anemia
- Neutropenia
- Thrombocytopenia
- Blood creatinine levels greater than 3.0 mg/dl
- Positive PPD without ongoing treatment for at least 30 days prior to study entry
- Pulmonary fibrotic changes
- Active infections (e.g., HIV, hepatitis B virus [HBV], hepatitis C virus [HCV])
and/or serologic evidence of prior exposure to hepatitis B
- Received a live vaccine within 3 months prior to study entry
- Doubled serum creatinine levels within the 3 months prior to study entry OR end-stage
kidney disease
- Dialysis-dependent end-stage kidney disease or membranous nephritis
- History of cancer. Individuals with a history of cervical carcinoma in situ and
resected basal and squamous cell carcinomas of the skin are not excluded.
- Receiving prednisone greater than 20 mg/day or equivalent corticosteroid treatment
- Pulse intravenous methylprednisolone within 30 days prior to study entry
- Receiving immunosuppressive agents other than prednisone, MMF, Mycophenolic Acid,
AZA, or hydroxychloroquine
- Oral or intravenous cyclosporine, leflunomide IVIG, or plasmapheresis within 3 months
prior to study entry
- Current or previous cyclophosphamide treatment
- Use of other experimental agent within 90 days prior to study entry
- Severe, progressive, or uncontrolled kidney, liver, blood, stomach, lung, heart, or
brain disease. Individuals with any of these conditions that are related to active
SLE are not excluded.
- Previous use of rituximab within 12 months prior to study entry
- Previous or current exposure to any of the following: etanercept (Enbrel), adalimumab
(Humira), infliximab (Remicade), or anakinra (Kineret)
- Meets New York Heart Association classification of congestive heart failure (CHF)
Class III or greater
- History of myocardial infarction or ischemia
- Current or history of substance abuse
- Known hypersensitivity to any component of the study drug
- Poorly controlled or advanced diabetes mellitus
- History of multiple sclerosis, transverse myelitis, optic neuritis, or epilepsy
- History of noncompliance with other therapies
- Pregnancy or breastfeeding |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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January 19, 2010 |
Modifications to
this listing: |
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Only selected fields are shown, please use the link
above to view all information about this clinical trial. |
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Clinical trials are medical research studies designed to test the safety and/or
effectiveness of new drugs, devices, or treatments in humans. These studies are
conducted worldwide for a range of conditions and illnesses. Learn more about
clinical research and participating in a study at
About Clinical Trials.
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