RAC December 4, 2002 - Presentation Materials
Day 1
Bethesda, Maryland

An Adverse Event in a Gene Transfer Clinical Trial for X-Linked Severe Combined Immunodeficiency Disease (SCID)  
  Theodore Friedmann, M.D., RAC Chair  
  Slides   
 

Review of FDA Biological Response Modifiers Advisory Committee Meeting  
  Stephanie L. Simek, Ph.D., U.S. Food and Drug Administration  
  Slides   
 

Review of October 29, 2002, RAC Planning Session  
  Stephen Rose, Ph.D., and/or Theodore Friedmann, M.D.  
  Slides   
 

Adverse Events in Clinical Trials Using Retroviral Vectors  
  Alexander Rakowsky, M.D., Office of Biotechnology Activities, NIH  
  Slides   
 

Monitoring Research Participants in Clinical Trials Using Retroviral Vectors  
  Theodore Friedmann, M.D., and Diane Wara, M.D., Moderator  
  Slides   
 

Monitoring for Insertional Oncogenesis and Clonality of Hemotopoiesis after Gene Therapy  
  Slides   
 

ADJOURN  
 


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