BASS XVII Tutorials and Keynote Address presentations:

SessionSpeakerPresentation
M-1Xiaolong Luo and Peter S. OuyangA Process View of Statistics for Clinical Trials: ANOVA, Product-Limit and Adaptive Design
M-2Qing Liu, Pilar Lim, Barry Schwab and Jaskaran SinghAdaptive Doubly-Randomized Delayed-Start Design and Applications to Anti-Depressant Drug Development
M-3Alex SverdlovCovariate-Adjusted Response-Adaptive Randomization Designs for Phase III Survival Trials
M-4Shanhong GuanSample Size Re-estimation in a Two-stage Design Using p-Value Combination Tests
M-5Tom StigerFailure-time Mixture Models for Analyzing Time to Response
M-6Jihong Chen and Jane QianEnrollment and Endpoint Projection in Oncology Clinical Trials
M-7Yoko TanakaStatistical Considerations in Multi-Regional Clinical Trials
Keynote AddressMohammad HuqueMultiplicity Problems in Controlled Clinical Trials: Regulatory Perspective
T-1Adam HammImplementing the Continous Reassessment Method (CRM) in a Phase I Oncology Trial
T-2Laszlo EndrenyiScaled Average Bioequivalence: An Approach to Resolve a Difficult Problem
T-3George Y. H. Chi and Gang LiA New Development and Perspective on the Design, Analysis & Interpretation of Non-inferiority Trials
T-4David Nelson and Carlos Alatorre
Methodological Considerations in Comparative Effectiveness Research
T-5Mark ReimersEstimation Issues in High-throughput Data Analysis
W-1Par KarlssonMultiple Testing in a Partitioning Framework
W-2Mohamed AloshRecent Developments in Addressing Multiplicity Issues in Clinical Trials
W-3Mohammad HuqueDecomposition of a Composite Endpoint for Assessing Treatment Benefits for its Components