Conference Theme
Subgroup Analysis in Clinical Trials: Opportunities and Challenges
Fees
• PENN faculty and students: $0
• Academic, Government, Non-Profit: $60
• Industry: $85
• Non-PENN students: $25
Co-Sponsors
American Statistical Association
Society for Clinical Trials
National Institute of Statistical Sciences
For additional information, contact:
Janine Pritchard
Phone: 215-573-4045 | Email: jpritcha@pennmedicine.upenn.edu
Agenda
MORNING SESSION
David Kent, MD (Tufts University)
Overview: Overall average treatment effects and one-variable-at-a-time subgroup analysis: The Scylla and Charybdis of Evidence Based Medicine
Ellis Unger, MD (Consultant)
An "unofficial" US Regulatory Perspective
Tom Fleming, PhD (University of Washington)
Pitfalls of subgroup analysis
Lisa McShane, PhD (NCI)
Finding the subgroup of patients who benefit from a novel therapy: no time for a game of hide and seek
AFTERNOON SESSION
Noah Simon, PhD (University of Washington)
Adaptive Enrichment Trials: Identifying the 'right' subgroup
Anastasia Ivanova, PhD (UNC)
Antimicrobial prophylaxis for vesicoureteral reflux: which children benefit the most?
Ilya Lipkovich, PhD (Eli Lilly)
Comparison of recent approaches for subgroup identification from clinical and observational data
Patrick Schnell, PhD (Ohio State)
Multiplicity considerations for analyses of non-exchangeable subgroups
PANELISTS
Mark Rothmann (FDA)
Kosuke Imai (Harvard)
Kit Roes (European Regulatory Perspective)
Michael Rosenblum (Johns Hopkins)
Janet Wittes (Statistics Collaborative, Inc.)
Event Type
- Affiliate Award Fund Eligible
- NISS Sponsored