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Use of Novel Biologics in the Treatment of Moderate to Severe Rheumatoid Arthritis
Series Overview
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How to Obtain AMA PRA Category 1 Credit(s)™

  1. Complete the CME case-based lesson.
  2. Login to your account.
  3. Complete the registration/ evaluation form.
  4. Print your personalized CME certificate.

Trials, Mechanisms, & New Agents in B-Cell–Directed Therapies: ENewsletter
Biotherapies

 
Technical Assistance:

(216) 448-0807
Monday—Friday
8 AM—5 PM
Eastern Time

 

 

 
Release Date: October 31, 2007 Expiration Date: October 31, 2008
 

Technical Requirements
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Accreditation

0.5 AMA PRA Category 1 Credit(s)TM.
Read the full Accreditation Statement

Target Audience

This activity is intended for rheumatologists, rheumatology fellows, and other health care professionals who treat patients with autoimmune rheumatic diseases.

Overview

The addition of the newer agents with novel mechanisms of action has expanded the armamentarium of biologic treatment options for the RA patient. With this expansion of therapeutic choices, several key clinical issues need to be addressed to ensure rational and clinically sound application of abatacept and rituximab in clinical practice including:

  • Protocols and procedures for overcoming inadequate response to TNF inhibition in moderate to severe RA
  • Protocols and procedures for maintenance therapy of new biologics
  • Short- and long-term safety issues and safety surveillance
  • Protocols and procedures for managing side effects
  • Improving physician-patient communication

Activity Design

The following activity utilizes an interactive, case-based format to identify, assess, and evaluate the available scientific research on and clinical experience with the use of rituximab and abatacept in patients with moderate to severe RA.

Objectives

At the conclusion of this activity, the participant will be able to:

  1. Identify strategies for treating patients who do not respond to newly-approved biologics.
  2. Discuss issues related to initiation and maintenance therapy with newly approved biologics.
  3. Address patients’ questions and concerns about newly approved biologics.

Activity Director

Leonard H. Calabrese, DO
Professor of Medicine
Vice Chairman, Department of Rheumatic and Immunologic Diseases
RJ Fasenmyer Chair of Clinical Immunology
Cleveland Clinic Lerner College of Medicine of Case Western Reserve University
Cleveland, Ohio

Author

Joel Kremer, MD

Faculty Disclosure

In accordance with the Standards for Commercial Support issued by the Accreditation Council for Continuing Medical Education (ACCME), The Cleveland Clinic Foundation Center for Continuing Education requires resolution of all faculty conflicts of interest to ensure CME activities are free of commercial bias.

The following faculty members have indicated they may have a relationship which, in the context of their presentations, could be perceived as a potential conflict of interest:

Leonard H. Calabrese, DO  
  Consulting, Teaching, and     Speaking Abbott Laboratories; Amgen Inc.; Genentech, Inc.
 
  Teaching and Speaking Bristol-Myers Squibb Company; Wyeth
 
  Consulting Biogen Idec; Hoffman-La Roche, Inc.
     
Joel Kremer, MD  
  Consulting, Teaching, Speaking, Grant Support Abbott Laboratories; Amgen Inc.; Bristol-Myers Squibb Company; Genentech, Inc.;
Hoffman-La Roche, Inc.

The Cleveland Clinic Foundation Center for Continuing Education acknowledges an educational grant for support of this activity from:

Genentech and Biogen Idec.

This CME activity was produced by The Cleveland Clinic Foundation Center for Continuing Education and Acumentis.

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