A Study to Evaluate the Safety and Tolerability of Multiple Intravenous Doses of MEDI 545 in Patients With Systemic Lupus Erythematosus

Exclusion Criteria

• - Have received MEDI-545 within 120 days prior to screening or have either detectable levels
• of MEDI-545 or anti-MEDI-545 antibodies (positive at > 1:10 serum dilution) in serum at screening;
• -History of allergy or reaction to any component of the study drug formulation;
• -Have received prednisone > 20 mg/day (or an equivalent dose of another oral corticosteroid)within 14 days before randomization/entry;
• -Have received the following dosages of medications within 28 days before
• randomization/entry: hydroxychloroquine > 600 mg/day, mycophenolate mofetil > 3 g/day,methotrexate > 25 mg/week, azathioprine > 3 mg/kg/day, or any dose of cyclophosphamide, cyclosporine, or thalidomide;
• -Have received leflunomide >20 mg/day in the 6 months prior to Study Day 0;
• -Have received fluctuating doses of antimalarials, mycophenolate mofetil, methotrexate,leflunomide, or azathioprine within 28 days before randomization/entry or fluctuating doses of NSAIDs or oral corticosteroids within 14 days before randomization/entry;
• -Treatment with any investigational drug therapy within 28 days before randomization/entry into the study, B cell-depleting therapies within 12 months before randomization/entry, or biologic therapies within 30 days or 5 half-lives of the biologic agent, whichever is longer,before randomization/entry into the study;
• -In the investigator's opinion, evidence of clinically significant active infection, including ongoing, chronic infection, within 28 days before randomization/entry;
• -A history of severe viral infection as judged by the investigators, including severe infections of either cytomegalovirus or the herpes family such as disseminated herpes, herpes encephalitis, ophthalmic herpes;
• -Herpes zoster infection within 3 months before randomization/entry;
• -Evidence of infection with hepatitis B or C virus, or HIV-1 or HIV-2, or active infection with hepatitis A, as determined by results of testing at screening;
• -Vaccination with live attenuated viruses within 28 days before randomization/entry;
• -Pregnancy (women, unless surgically sterile or at least 2 years post-menopausal, must have a negative serum pregnancy test within 28 days before receiving the study drug and a negative urine pregnancy test on Study Day 0 before receiving the study drug);
• -Breastfeeding or lactating women;
• -History of primary immunodeficiency;
• -History of alcohol or drug abuse < 1 year prior to randomization/entry;
• -History of cancer (except basal cell carcinoma or in situ carcinoma of the cervix treated with apparent success with curative therapy > 1 year prior to randomization/entry);
• - History of active TB infection;
• -History of latent TB infection or newly positive TB skin test (reaction defined as ≥ 10 mm in diameter if not on systemic immunosuppressive medication or ≥ 5 mm if on systemic immunosuppressive medication) without completion of an appropriate course of treatment or with ongoing prophylactic therapy;
• -Elective surgery planned from the time of screening through Study Day 196;
• -At screening blood tests (within 28 days before randomization/entry), any of the following:
• • AST > 2 × upper limit of normal range (ULN), unless caused by SLE, as determined by the investigator,
• • ALT > 2 × ULN,unless caused by SLE, as determined by the investigator,
• • Creatinine > 4.0 mg/dL,
• • Neutrophils "1,500/ μL (< 1.5 × 109/L)”
• • Platelet count “Platelet count < 50,000/ μL (< 50 × 109/L)”
• -History of any disease, evidence of any current disease (other than SLE), any finding upon physical examination, or any laboratory abnormality that, in the opinion of the investigator or medical monitor, may compromise the safety of the patient in the study or confound the analysis of the study; or
• -Any employee of the research site who is involved with the conduct of the study.