May 16, 2018: This workshop explored challenges and strategies for planning and implementing ePCTs that compare two or more therapeutic medical regimens.
Agenda and Slides
Welcome and Introduction
David Shurtleff, PhD
Richard Hodes, MD
Catherine Meyers, MD
Wendy Weber, PhD, MPH
Panel 1: Partnering With Stakeholders to Conduct Embedded A vs. B Trials: Keys to Success
Moderator: Rich Platt, MD, MSc
Panel:
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- Steve Friedhoff, MD
- Kenneth Sands, MD, MPH
- Joseph Chin, MD
Panel 2: Examples in Action: Embedded A vs. B Trials
Moderator: Beverly Green, MD, MPH
Panel:
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- Ryan Ferguson, ScD, MPH
- Susan Huang, MD, MPH
- Michael Kappelman, MD, MPH
Panel 3: Maximizing the Pragmatic: Understanding Approaches to Design of Embedded A vs. B Trials
Moderator: Greg Simon, MD, MPH
Panel:
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- Scott Solomon, MD
- Rachael Fleurence, PhD
- Kourtney Davis, PhD, MSPH
Panel 4: Regulatory Aspects of Clinical Research and the Regulation of Products for Embedded A vs. B Pragmatic Trials
Moderator: Adrian Hernandez, MD
Panel:
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- Jacqueline Corrigan-Curay, MD, JD
- Owen Faris, PhD
- Julie Kaneshiro, MA
Panel 5: Ethical and IRB Approaches for a Successful Embedded A vs. B Pragmatic Trials Moderator:
Moderator: David Wendler, PhD
Panel:
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- Barbara Bierer, MD
- Spencer Hey, PhD
- Judith Carrithers, JD, MPA
Summary and Concluding Remarks
Moderator: Cathy Meyers, MD
Panel:
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- Adrian Hernandez, MD
- Rich Platt, MD, MSc
- Beverly Green, MD, MPH
- Greg Simon, MD, MPH
- Dave Wendler, PhD