| Learning
Objectives •
Describe
the similarities and differences among biologic agents in achieving rapid
induction and • Explain the clinical value of early use of biologic therapy in CD • Define practical considerations for the optimal use of biologics in CD, including patient selection, timing of therapy, dosing, and use of biologics alone or in combination with immunosuppressive agents • Describe the long-term safety of biologics and the benefit-risk profile of these agents Educational
Method Target
Audience CME
Accreditation Chicago Medical School at Rosalind Franklin University of Medicine and Science designates this educational activity for a maximum of 2.0 AMA PRA Category 1 Credits™. Physicians should only claim credit commensurate with the extent of their participation in the activity. Faculty DisclosuresWilliam J. Sandborn, MD: Research Support: Abbott,Centocor, Schering-Plough, UCB Pharma; Consultant: Abbott, Centocor, Elan Pharmaceuticals, UCB Pharma; Advisory Board: Abbott, Centocor, Elan Pharmaceuticals, UCB Pharma. |
Stefan Schreiber, MD: Consultant: Abbott, Bristol-Myers Squibb, Centocor, Essex Pharmaceuticals, Schering-Plough, UCB Celltech; Advisory Board: Abbott, Bristol-Myers Squibb, Centocor, Chemocentryx, Essex Pharma, Schering-Plough, UCB Celltech; Speakers’ Bureau: Abbott, Centocor, Essex Pharma, Schering-Plough, UCB Celltech; Stockholder: CONARIS Research Institute AG. Remo
Panaccione, MD: Research Support: Bruce E. Sands, MD, MS: Research Support: Abbott, Centocor; Consultant: Abbott, Biogen IDEC, Centocor, Elan Pharmaceuticals, UCB Pharma; Advisory Board: Abbott, Centocor, Elan Pharmaceuticals, UCB Pharma; Speakers’ Bureau: Abbott, Centocor, Elan Pharmaceuticals, UCB Pharma. Support Expiration
Date Post-test
Certificates of CME credit will be issued by The Chicago Medical School at Rosalind Franklin University of Medicine |
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