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CNS Clinical Trials: Suicidality and Data Collection: Workshop Summary (2010)

Chapter: Appendix C: Workshop Attendees

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Suggested Citation:"Appendix C: Workshop Attendees." Institute of Medicine. 2010. CNS Clinical Trials: Suicidality and Data Collection: Workshop Summary. Washington, DC: The National Academies Press. doi: 10.17226/12829.
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Page 61
Suggested Citation:"Appendix C: Workshop Attendees." Institute of Medicine. 2010. CNS Clinical Trials: Suicidality and Data Collection: Workshop Summary. Washington, DC: The National Academies Press. doi: 10.17226/12829.
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Page 62
Suggested Citation:"Appendix C: Workshop Attendees." Institute of Medicine. 2010. CNS Clinical Trials: Suicidality and Data Collection: Workshop Summary. Washington, DC: The National Academies Press. doi: 10.17226/12829.
×
Page 63
Suggested Citation:"Appendix C: Workshop Attendees." Institute of Medicine. 2010. CNS Clinical Trials: Suicidality and Data Collection: Workshop Summary. Washington, DC: The National Academies Press. doi: 10.17226/12829.
×
Page 64

Below is the uncorrected machine-read text of this chapter, intended to provide our own search engines and external engines with highly rich, chapter-representative searchable text of each book. Because it is UNCORRECTED material, please consider the following text as a useful but insufficient proxy for the authoritative book pages.

C Workshop Attendees Omar Ali Rosina Dixon i3 Statprobe Sanofi-Aventis Larry Alphs Sarah DuBrava Ortho-McNeil Janssen Pfizer Scientific Affairs, LLC Amy Ellis Mark Bangs MedAvante Eli Lilly and Company Reuven Ferziger Hendricks Brown University of Miami Regan Fong GlaxoSmithKline Pilar Cazorla Richard Frank Kathryn Connor GE Healthcare Merck Research Laboratories Harry Gedney Vladimir Coric National Park Service Bristol-Myers Squibb Alan Gelenberg Brenda Crowe Healthcare Technology Eli Lilly and Company Systems, Inc. 61

62 CNS CLINICAL TRIALS: SUICIDALITY AND DATA COLLECTION Paul Gilbert Anne Libby MedAvante University of Colorado at Denver Laurence Greenhill Alan Lipschitz Owen Hagino GlaxoSmithKline Sanofi-Aventis Clare Makumi Richard Hodes GlaxoSmithKline National Institutes of Health Randall Marshall Yiqun Hu Sepracor, Inc. FRI Roger Meyer Joseph Hulihan Best Practice Project Ortho-McNeil Janssen Management, Inc. Scientific Affairs Tanya Momtahen Neely Ivgy-May Sanofi-Aventis Schering Plough Corp. Sanjeer Pathak Thomas Konechnik Eli Lilly and Company Jane Pearson National Institute of Mental Stephen H. Koslow Health American Foundation for Suicide Prevention David Sheehan University of South Florida Mary Kujawa College of Medicine Hoffmann-LaRoche, Inc. Peter Sorantin Deborah Lazzaretto MedAvante New York State Psychiatric Institute Susanne Steinberg Pfizer Susi Lee Merck & Co., Inc Vani Vannappagari GlaxoSmithKline

APPENDIX C 63 Lingfeng Yang Wyeth Research Kseniya Yershova New York State Psychiatric Institute/Columbia University

Next: Appendix D: Biographical Sketches of Invited Speakers »
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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.

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