To be alerted when registration for the 2020 course opens, please email clinicalinvestigator@fda.hhs.
The audio recordings from this event are now available online via Adobe Connect:
Download the Agenda (PDF)
Welcome and Introduction |
Susan McCune, M.D. |
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Keynote Speaker and Setting the Stage |
Bridgette Jones, M.D. |
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Label Enabling Clinical Trials |
William Smoyer, M.D. |
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Hot Topics |
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Extrapolation and Innovative Trial Designs |
Yodit Belew, M.D. |
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Molecular Targets -- Oncology |
Greg Reaman, M.D. |
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Enrolling Pediatric Patients in Adult Trials |
Tara Altepeter, M.D. |
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Break |
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The Basics
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Opening an IND |
Michael Cohen-Wolkowiez, M.D. |
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FDA Perspective of Study Design and Plan, Dose Selection |
John Alexander, M.D. Division of Pediatric and Maternal Health Food and Drug Administration |
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Ethical Considerations |
Melanie Bhatnagar, M.D. |
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Pediatric Formulations |
Julia Pinto, Ph.D. |
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Non-clinical Data Requirements |
Karen Davis-Bruno, Ph.D. Food and Drug Administration |
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Good Clinical Practice and Understanding the Regulations |
Susan Leibenhaut, M.D.
Food and Drug Administration
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Safety Considerations: Regulatory Definitions and Practical Considerations |
Ramy Abdelrahman, M.D.
Food and Drug Administration
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Discussion/Case Presentation |
Michael Cohen-Wolkowiez, M.D.
Pediatric Trials Network
Jonathan Davis, M.D.
Tufts Medical Center
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Lunch
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Pediatric Trial Funding and Engagement Panel Discussion |
Rohan Hazra, M.D. (NIH/NICHD) Jonathan Davis, M.D. (Clinical and Translational Science Awards) Michael Cohen-Wolkowiez, M.D. (Duke University) Ed Connor, M.D. (Institute for Advance Clinical Trials for Children) Bridgette Jones, M.D. (AAP) Steven Hirschfeld, M.D., Ph.D. (NIH/NIDCD) |
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Practical Applications with Case Studies
Moderator: Lynne Yao, M.D.
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Table Moderators |
Susan McCune, M.D. |
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Break |
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