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Bethesda North Marriott Hotel and Conference Center

20 sep 2018 7:00 a.m. - 21 sep 2018 12:45 p.m.

5701 Marinelli Road, , North Bethesda, MD 20852 , USA

Advancing the Science of Study Endpoints

Session 4: Regulatory Update

Session Chair(s)

Ashley F. Slagle, PHD, MS

Ashley F. Slagle, PHD, MS

Principal, Scientific and Regulatory Consulting, Aspen Consulting, LLC, United States

Hear timely updates from FDA representatives on the 21st Century Cures Act provision to expand the qualification and use of drug development tools (DDTs) to support the drug development process. Attendees will hear an update on FDA’s patient-focused drug development, including their thoughts on leveraging COAs in cancer clinical trials.

Speaker(s)

Paul  Kluetz, MD

Paul Kluetz, MD

Deputy Director, Oncology Center of Excellence, OC, FDA, United States

Elektra  Papadopoulos, MD, MPH

Elektra Papadopoulos, MD, MPH

Director, Patient Experience Data and Strategy, AbbVie, United States

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