CNS Clinical Trials:

Suicidality and Data Collection: Workshop Summary

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Size: 88 pages, 6x9

Publication Year:2010

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PAPERBACK ISBN-10: 0-309-14883-9 ISBN-13: 978-0-309-14883-2	$21.00	Add to Cart

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Authors:
Sarah Hanson, Miriam Davis, and Bruce Altevogt, Rapporteurs; Forum on Neuroscience and Nervous System Disorders
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Table of Contents
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Front Matter	i-xii
Introduction	1-6	(skim)
1 Perspectives from the FDA, Academia, and Patients	7-16	(skim)
2 Data Collection and Optimization	17-24	(skim)
3 Data Analysis	25-34	(skim)
4 Partnerships, Opportunities, Collaboration	35-42	(skim)
Appendix A: References	43-50	(skim)
Appendix B: Workshop Agenda	51-60	(skim)
Appendix C: Workshop Attendees	61-64	(skim)
Appendix D: Biographical Sketches of Invited Speakers	65-76	(skim)

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The Food and Drug Administration (FDA) now requires that all clinical trials for drugs that affect the central nervous system--including psychiatric drugs--are assessed for whether that drug might cause suicidal ideation or behavior. The Institute of Medicine's (IOM) Forum on Neuroscience and Nervous System Disorders hosted a meeting on June 26, 2009, to discuss the FDA's new policy and how to analyze best whether suicidal thoughts predict actual suicidal behavior in the near future.

CNS Clinical Trials:

Suicidality and Data Collection: Workshop Summary

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