
eBook - PDF
Clinical Trial Biostatistics and Biopharmaceutical Applications
- 580 pages
- English
- PDF
- Available on iOS & Android
eBook - PDF
Clinical Trial Biostatistics and Biopharmaceutical Applications
About this book
Since 1945, "The Annual Deming Conference on Applied Statistics" has been an important event in the statistics profession. In Clinical Trial Biostatistics and Biopharmaceutical Applications, prominent speakers from past Deming conferences present novel biostatistical methodologies in clinical trials as well as up-to-date biostatistical applications
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Yes, you can access Clinical Trial Biostatistics and Biopharmaceutical Applications by Walter R. Young, Ding-Geng (Din) Chen in PDF and/or ePUB format, as well as other popular books in Mathematics & Probability & Statistics. We have over one million books available in our catalogue for you to explore.
Information
Table of contents
- Front Cover
- Contents
- List of Figures
- List of Tables
- Preface
- Early History of the DemingConference
- Some Nonstatistical Reminiscences of My 44 Years of Chairing the Deming Conference
- Contributors
- Section I: Emerging Issues in ClinicalTrial Design and Analysis
- Chapter 1: Emerging Challenges of Clinical Trial Methodologies in Regulatory Applications
- Chapter 2: Review of Randomization Methodsin Clinical Trials
- Chapter 3: First Dose Ranging Clinical Trial Design:More Doses? Or aWider Range?
- Chapter 4: Thorough QT/QTc Clinical Trials
- Chapter 5: Controversial (Unresolved) Issues in Noninferiority Trials
- Section II: Adaptive Clinical Trials
- Chapter 6: Adaptive Designs in Drug Development
- Chapter 7: Optimizing Group-Sequential Designs with Focus on Adaptability: Implications of Nonproportional Hazards in Clinical Trials
- Chapter 8: Group Sequential Design in R
- Section III: Clinical Trials in Oncology
- Chapter 9: Issues in the Design and Analysis of Oncology Clinical Trials
- Chapter 10: Competing Risks and Their Applications in Cancer Clinical Trials
- Chapter 11: Dose Finding with Escalation with Overdose Control in Cancer Clinical Trials
- Chapter 12: Interval-Censored Time-to-Event Data andT heir Applications in Clinical Trials
- Section IV: Multiple Comparisons in Clinical Trials
- Chapter 13: Introduction to Multiple Test Problems, with Applications to Adaptive Designs
- Chapter 14: Graphical Approaches to Multiple Testing
- Chapter 15: Pairwise Comparisons with Binary Responses: Multiplicity-Adjusted P-Values and Simultaneous Confidence Intervals
- Chapter 16: Comparative Study of Five Weighted Parametric Multiple Testing Methods for Correlated Multiple Endpoints in Clinical Trials
- Section V: Clinical Trials in a Genomic Era
- Chapter 17: Statistical Analysis of Biomarkers from -Omics Technologies
- Chapter 18: Understanding Therapeutic Pathways via Biomarkers and Other Uses of Biomarkers in Clinical Studies
- Chapter 19: Statistical Evaluation of Surrogate Endpoints in Clinical Studies
- Back Cover