Accepts Healthy Volunteers
Healthy volunteers are participants who do not have a disease or condition, or related conditions or symptoms
An interventional clinical study is where participants are assigned to receive one or more interventions (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes.
An observational clinical study is where participants identified as belonging to study groups are assessed for biomedical or health outcomes.
Searching Both is inclusive of interventional and observational studies.
|Eligible Ages||18 Years and Over|
Inclusion Criteria:1. Meet at least 4 of the 11 American College of Rheumatology (ACR) 1997 criteria for classification of SLE (see Appendix 1).OR meet the recent classification recommended by SLICC (Appendix 2) 6 2. ≥3 swollen and tender joints on 2 examinations at least 2 weeks apart and no more than 8 weeks apart. 3. SLEDAI2K score ≥4 indicating active disease. 4. Documented positive ANA (≥1:80) and/or anti-dsDNA during course of SLE. 5. Men and women, at least 18 years of age. Women of childbearing potential must use adequate method(s) of contraception to avoid pregnancy throughout the study and for up to 2 months after last study drug dose. They must have a negative serum or urine pregnancy test prior to the start of study medication. 6. Background therapies allowed: antimalarials (dose constant for ≥ one month before study entry and during 16 weeks of trial), methotrexate (same criteria as for antimalarials), azathioprine (same criteria), mycophenolate (same criteria), leflunomide (same criteria). During the screening period and for up to 6 weeks after randomization, a daily prednisone (or equivalent) regimen of up to 20 mg daily may be initiated to treat the moderate to severe disease activity present at screening. The initial steroid regimen is not required if investigators or patients believe that the risks would outweigh the potential benefits. Patients who do not take any glucocorticoids during the study will be included in the treatment groups and analysis. *Steroids should be tapered to a target dose of no more than 10 mg/day of prednisone (or equivalent) by the end of Week 8 (Day 56). The steroid regimen should be tapered as quickly as safely possible. Prednisone dose requirements higher than 10 mg daily at the 8 week visit will cause the patient to be ruled a non-responder for the abatacept treatment arm.
Exclusion Criteria:1. Subjects with active infection requiring oral or IV antibiotics within one month of first dose of study medication. 2. Subjects with BILAG A in any system outside the musculoskeletal system. 3. Subjects with positive quantiferon Gold test in the absence of treatment for tuberculosis. 4. Subjects with positive tests for active infection with hepatitis B or C during the past 6 months. Any confirmed positive test for HIV at any time prior to entry into this study. 5. Subjects with active glomerulonephritis (>3 g protein/24h and/or active urine sediment). 6. Subjects with active CNS disease. 7. Subjects with any other serious disease that would require immunosuppressive or parenteral anti-microbial therapy outside the study protocol. 8. Inability to self-administer subcutaneous injections, to comply with instructions, or to keep appointments for study visits. 9. Treatment with rituximab within the past 6 months (B cells must be detectable in peripheral blood at onset of treatment with study biologic), belimumab within the past 5 months, cyclophosphamide within the past 3 months. 10. Treatment with any other immunomodulatory biologic or cyclophosphamide during treatment with abatacept is not allowed. 11. Patients requiring >20 mg of prednisone daily. 12. Women who are pregnant or breast feeding. 13. Women of child bearing potential unwilling or unable to use an acceptable method to avoid pregnancy for the entire study period and for up to 2 months after last study drug. 14. Subjects with a history of cancer within the last five years (other than non-melanoma skin cell cancers cured by local resection). 15. Any laboratory test results that, in the opinion of the Investigator, might place the subject at unacceptable risk for participation in this study.
This trial id was obtained from ClinicalTrials.gov, a service of the U.S. National Institutes of Health, providing information on publicly and privately supported clinical studies of human participants with locations in all 50 States and in 196 countries.
Phase 1: Studies that emphasize safety and how the drug is metabolized and excreted in humans.
Phase 2: Studies that gather preliminary data on effectiveness (whether the drug works in people who have a certain disease or condition) and additional safety data.
Phase 3: Studies that gather more information about safety and effectiveness by studying different populations and different dosages and by using the drug in combination with other drugs.
Phase 4: Studies occurring after FDA has approved a drug for marketing, efficacy, or optimal use.
|Phase 1/Phase 2|
The sponsor is the organization or person who oversees the clinical study and is responsible for analyzing the study data.
|University of California, Los Angeles|
The person who is responsible for the scientific and technical direction of the entire clinical study.
|Bevra Hahn, M.D.|
|Principal Investigator Affiliation||University of California, Los Angeles|
Category of organization(s) involved as sponsor (and collaborator) supporting the trial.
The disease, disorder, syndrome, illness, or injury that is being studied.
|Systemic Lupus Erythematosus Arthritis|
Contact a Trial Team
If you are interested in learning more about this trial, find the trial site nearest to your location and contact the site coordinator via email or phone. We also strongly recommend that you consult with your healthcare provider about the trials that may interest you and refer to our terms of service below.