Clinical Trial Biostatistics and Biopharmaceutical Applications -

Clinical Trial Biostatistics and Biopharmaceutical Applications

Buch | Softcover
580 Seiten
2020
Chapman & Hall/CRC (Verlag)
978-0-367-57603-5 (ISBN)
57,35 inkl. MwSt
With contributions from leaders in the biostatistical community, this book presents novel biostatistical methodologies in clinical trials as well as up-to-date biostatistical applications from the pharmaceutical industry. It covers emerging issues in clinical trial design and analysis, adaptive clinical trial designs, oncology clinical trials, m
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 from the pharmaceutical industry.



Divided into five sections, the book begins with emerging issues in clinical trial design and analysis, including the roles of modeling and simulation, the pros and cons of randomization procedures, the design of Phase II dose-ranging trials, thorough QT/QTc clinical trials, and assay sensitivity and the constancy assumption in noninferiority trials. The second section examines adaptive designs in drug development, discusses the consequences of group-sequential and adaptive designs, and illustrates group sequential design in R. The third section focuses on oncology clinical trials, covering competing risks, escalation with overdose control (EWOC) dose finding, and interval-censored time-to-event data.



In the fourth section, the book describes multiple test problems with applications to adaptive designs, graphical approaches to multiple testing, the estimation of simultaneous confidence intervals for multiple comparisons, and weighted parametric multiple testing methods. The final section discusses the statistical analysis of biomarkers from omics technologies, biomarker strategies applicable to clinical development, and the statistical evaluation of surrogate endpoints.



This book clarifies important issues when designing and analyzing clinical trials, including several misunderstood and unresolved challenges. It will help readers choose the right method for their biostatistical application. Each chapter is self-contained with references.

Walter R. Young, Ding-Geng Chen

Emerging Issues in Clinical Trial Design and Analysis. Adaptive Clinical Trials. Clinical Trials in Oncology. Multiple Comparisons in Clinical Trials. Clinical Trials in the Genomic Era. Index.

Erscheinungsdatum
Sprache englisch
Maße 156 x 234 mm
Gewicht 1070 g
Themenwelt Mathematik / Informatik Mathematik
Studium Querschnittsbereiche Epidemiologie / Med. Biometrie
Naturwissenschaften Biologie
Technik
ISBN-10 0-367-57603-1 / 0367576031
ISBN-13 978-0-367-57603-5 / 9780367576035
Zustand Neuware
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