Study of MEDI-522 Administered by Subcutaneous Injection to Adults With Plaque Psoriasis

Exclusion Criteria

• •Pustular, guttate, or erythrodermic psoriasis as the predominant disease type
• •Evidence of active hepatitis A, hepatitis B virus (HBV) or hepatitis C virus (HCV) infection, such as positive HBsAg or positive anti-hepatitis C antibody
• •Pregnancy (must have a negative serum pregnancy test within 21 days prior to the first dose of study drug, and urine pregnancy test must be negative on Study Day 0 before study entry)
• •History of cancer (except excision of basal cell carcinoma)
• •Evidence of significant active infection, such as fever less than or greater to 38.0°C (100.5°F), or chronic systemic infection
• •Known or suspected infection with human immunodeficiency virus (HIV) or other evidence of clinically significant immune deficiencies
• •Diagnosis of psoriatic arthritis or rheumatoid arthritis requiring active treatment
• •History of hematuria due to chronic cystitis, recurrent kidney stones, or nephritis, history of CVA, poorly controlled hypertension, angina, stable abdominal aneurysm, recent superficial phlebitis, or recent myocardial infarction (within past 1 year without definitive corrective surgery such as coronary bypass graft or angioplasty)
• •Receipt of systemic therapy for psoriasis or immunosuppressive medication in the past 4 weeks, including systemic retinoids, systemic steroids (oral, IM, or IV), cyclosporine A,methotrexate, azathioprine, anti-TNF agents, anti-T-cell agents, phototherapy (PUVA, UVB,tanning bed use), coal tar treatment (Goeckerman or modified Goeckerman regimen), tacrolimus, or mycophenolate
• •Use of topical therapy for psoriasis in the past 2 weeks, such as steroid containing creams, Vitamin D analog creams and coal tar shampoos
• •Receipt of any investigational drug therapy within 4 weeks before the first dose of study drug in this protocol (use of licensed agents for indications not listed in the package insert is permitted)
• •Current or planned participation in a research protocol in which an investigational agent or therapy may be administered
• •History of allergic disease or reactions likely to be exacerbated by any component of MEDI-522
• •Nursing mother
• •Evidence of acute illness
• •Clinical manifestations of significant end organ dysfunction or failure that may compromise the safety of the patient in the study
• •History of gastrointestinal bleeding (i.e., stool positive for occult blood or overt bleeding) within the previous 6 months
• •Known bleeding disorder or significant risk of clinically important abnormal bleeding due to anticoagulant therapy with warfarin or heparin
• •Insulin-dependent diabetes mellitus that is recent-onset or unstable
• •Elective surgery planned during the study period through Study Day 167