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Bethesda North Marriott Hotel and Conference Center

Apr 08, 2019 1:00 PM - Apr 10, 2019 4:00 PM

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

DIA/FDA Biostatistics Industry and Regulator Forum

Session 9:Unhealthy Safety Assessment: Moving Towards Better Characterization of Patient Harms

Session Chair(s)

Mat  Soukup, PhD

Mat Soukup, PhD

Deputy Director, Division of Biometrics VII, OB, OTS CDER, FDA, United States

Brenda  Crowe, PhD

Brenda Crowe, PhD

Associate Vice President, Statistics, Eli Lilly and Company, United States

Frank W. Rockhold, PhD, MSc

Frank W. Rockhold, PhD, MSc

Professor of Biostatistics, Duke Clinical Research Institute, Duke University Medical Center, United States

The amount of information collected in clinical trials is weighted more to safety than benefit; however, a disproportionate number of statisticians are involved in assessing the benefits of a pharmaceutical product relative to the number of statisticians assessing the risks. This is also reflected in the literature around new medicines. It is important for there to be a statistical presence in the evaluation of safety as the questions can be complex and require novel statistical solutions; even in simple cases, such as calculating rates across trials, a lack of statistical presence has resulted in inadequate and improper approaches being utilized.

Learning Objective : At the conclusion of this session, participants should be able to:
  • Understand common clinical issues that arise when characterizing the safety (and benefit-risk) of a pharmaceutical product
  • Identify the rationale and motivation for an increased statistical presence in assessing risks
  • Apply good statistical practice for safety related topics

Speaker(s)

Christopher B. Granger, MD

Christopher B. Granger, MD

Professor of Medicine; Director, Cardiac Intensive Care Unit, Duke University Medical Center, United States

Unhealthy Safety Assessment: Moving Towards Better Characterization of Patient Harms

Steffen  Unkel

Steffen Unkel

Department of Medical Statistics, University Medical Center Göttingen, Germany

Estimands and the Analysis of Adverse Events in the Presence of Varying Follow-Up Times Within the Benefit Assessment of Therapies

Peter  Stein, MD

Peter Stein, MD

Consultant, Peter Stein Consulting, LLC, United States

Improved Characterization of Patient Harms: A Regulatory Perspective

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