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Bethesda North Marriott Hotel and Conference Center

2019 年 04 月 08 日 1:00 下午 - 2019 年 04 月 10 日 4:00 下午

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

DIA/FDA Biostatistics Industry and Regulator Forum

Session 6: Master Protocols: Design Considerations and Operational Examples (Case-Studies)

Session Chair(s)

Jonathan  Haddad, MPH

Jonathan Haddad, MPH

HIV Disease Area Head, Clinical Statistics

GlaxoSmithKline, United States

Min  Lin, MD, PhD

Min Lin, MD, PhD

Statistical Science Director

Astrazeneca, United States

Amy  Xia, PhD

Amy Xia, PhD

Vice President, Center for Design and Analysis

Amgen Inc., United States

This session will explore the design considerations and operational challenges for Master Protocols. A brief presentation of the key challenges and opportunities will be followed by a review of one or more case-studies. A multi-disciplinary panel will then discuss the statistical and operational aspects that contribute to the success (or failure) of Master Protocols.

Learning Objective : At the conclusion of this session, participants should be able to:
  • Understand the most common designs using Master Protocols and their utility in solving clinical development challenges
  • Understand the operational challenges and considerations in executing Master Protocols
  • Gain awareness to the pros, cons, and common mistakes for Master Protocol designs through a panel discussion

Speaker(s)

Scott  Berry, PhD

A Brief Overview

Scott Berry, PhD

Berry Consultants LLC, United States

President and Senior Statistical Scientist

Melissa   Paoloni

Speaker

Melissa Paoloni

Arcus Bioscience, United States

VP, Medical Affairs & Clinical Partnerships

Sofia  Paul, PhD

Master Protocols: Design Considerations and Operational Examples (Case-Studies)

Sofia Paul, PhD

GSK, United States

Senior Director

Shenghui  Tang

Panelist

Shenghui Tang

FDA, United States

Team leader, Division of Biometrics V of the Office of Biostatistics,CDER

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