2024 Conference on Statistical Issues in Clinical Trials

2024 Conference on Statistical Issues in Clinical Trials

16th Annual Conference on Statistical Issues in Clinical Trials:
Optimizing Dose Selection Across the Clinical Trials Spectrum

April 18, 2024

8:15a - 4:30p


Recording of Sessions

  • AM Session
  • PM Session

Click on the topic title to access the slides.


Speakers/Panelists Topics
Frank Bretz, PhD
Novartis AG
Overview: Dose-Response Characterization: A Key to Success in Drug Development
Joyce Cheng, PhD
Food and Drug Administration
Regulatory Perspectives on Dosage Optimization for Oncology Drugs
Ying Yuan, PhD
UT MD Anderson Cancer Center
Statistical Designs and Strategies for Dose Optimization
Man (Mandy) Jin, PhD
Abbvie, Inc.
Comparison of Adaptive Seamless Phase 2/3 Designs with Dose Selection and Multiple Endpoints
AM Panelists

Elizabeth Garrett-Mayer, PhD
American Society of Clinical Oncology

Ken Cheung, PhD
Columbia University Mailman School of Public Health
Optimizing Dose Selection Across the Clinical Trials Spectrum: Thoughts on the Morning Session

Weng Kee Wong, PhD
UCLA Fielding School of Public Health
Nature-Inspired Meta-Heuristic Algorithms for Constructing Efficient Designs for Clinical Trials
Pavel Mozgunov, PhD
MRC Biostatistics Unit, University of Cambridge
Practical Implementation of a Model-based Design in a Phase I Combination-schedule Dose-finding Trial
Michael Kosorok, PhD
UNC Gillings School of Global Public Health
A SMART Clinical Trial for Chronic Lower Back Pain
Yunda Huang, PhD
Fred Hutch Cancer Center
Dose Finding in HIV-1 Preventive Vaccine and Monoclonal Antibody Trials
PM Panelists

Anna Heath, PhD
SickKids Research Institute

Kelley Kidwell, PhD
University of Michigan School of Public Health



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