Study of Tysabri (Natalizumab) in Patients Who Failed Anti-TNF-α Therapy

Exclusion Criteria

• •1. Women of childbearing potential unless surgically sterile or using adequate contraception (IUD, oral or depot contraceptive, or barrier plus spermicide), and willing and able to continue contraception for 3 months after the last infusion of study drug (i.e., up to Week 20). Women using oral contraception must have started using it at least 2 months prior to enrollment;
• •2. Women who are pregnant or breastfeeding;
• •3. Prior treatment with TYSABRI® (natalizumab) (also referred to as Antegren™ in previous clinical trials);
• •4. Symptoms suggestive of intestinal stricture or obstruction;
• •5. History of cancer or lymphoproliferative disease other than a successfully and completely treated squamous cell or basal cell carcinoma of the skin;
• •6. Patients with a history of Listeria or human immunodeficiency virus (HIV) or a history of previously untreated TB;
• •7. Patients who have had surgical bowel resections in the past 2 weeks or are planning any resection within 4 weeks of starting the study medication;
• •8. Patients who do not meet any of the following criteria regarding baseline medications for CD (Please note that the term "Week 0" below refers to the exact day of the baseline visit):
• •1. Baseline use of anti-tumor necrosis factor (anti-TNF-α) therapy, or previous use of all three approved agents, is not permitted;
• •2. Baseline use of azathioprine (AZA), 6 mercaptopurine (6MP) / 6 thioguanine (6TG) / methotrexate (MTX) is not permitted;
• •3. Baseline use of any other immunosuppressant (e.g., tacrolimus, cyclosporin, mycophenolate mofetil or leflunomide) is not permitted;
• •4. Experimental agents must have been discontinued at least 4 weeks prior to Week 0, or for a period equivalent to 5 half-lives (t½) of the agent (whichever is longer);
• •5. Any baseline 5-Aminosalicylate (5 ASA) compounds or antibiotics are permitted and if used must be continued at a stable dose during the trial;
• •6. Any baseline 5-Aminosalicylate (5 ASA) compounds or antibiotics must have been administered at a stable dose for a minimum of 4 weeks prior to Week 0;
• •7. Any baseline use of budesonide must have been administered at a stable dose for a minimum of 2 weeks prior to Week 0;
• •8. For oral steroids other than budesonide, patients must have been at a stable dose for a minimum of 2 weeks prior to Week 0;
• •9. Patients likely to require emergency surgery for persistent intestinal obstruction, bowel perforation, uncontrolled bleeding or abdominal abscess infection, and patients who have undergone bowel surgery, including resections, within the 3 months prior to Week 0;
• •10. Patients who have a colostomy, ileostomy, or colectomy with ileorectal anastomosis;
• •11. Ileal resections resulting in clinically relevant short bowel syndrome, in the opinion of the Investigator;
• •12. Patients who are receiving or have received nasogastric/nasoenteric tube feeding, an elemental diet, or total parenteral nutrition (TPN) within the 2 weeks prior to Week 0;
• •13. Patients with a chest X-ray suggestive of pulmonary infection at screening;
• •14. Patients with a history of clinically significant and/or persistent gastrointestinal disorder (other than CD), cardiovascular, renal, hepatic, neurological, dermatological, immunological, major psychiatric (including drug or alcohol abusers), or hematological illness;
• •15. Patients with any laboratory tests considered clinically significant at screening;
• •16. Patients whose symptoms are likely caused by factors other than inflammatory CD, including infection, irritable bowel syndrome (IBS), or ulcerative colitis (UC);
• •17. Patients who will be unavailable for the duration of the trial, likely to be noncompliant with the protocol, or who are felt to be unsuitable by the Investigator for any other reason;
• •18. Patients who have do not have evidence of active inflammation.
• •19. Patients with active opportunistic infection or history of opportunistic infection in the last 6 month.