Contemporary Biostatistics with Biopharmaceutical Applications

This is a preview of subscription content, log in via an institution to check access.

Access this book

Subscribe and save

Springer+ Basic €32.70 /Month

Buy Now

Price includes VAT (France)

Softcover Book EUR 105.49

Price includes VAT (France)

Hardcover Book EUR 105.49

Price includes VAT (France)

Tax calculation will be finalised at checkout

Other ways to access

About this book

This edited volume presents current research in biostatistics with emphasis on biopharmaceutical applications. Featuring contributions presented at the 2017 ICSA Applied Statistics Symposium held in Chicago, IL on June 25 to 28, 2017, this book explores timely topics that have a high potential impact on statistical methodology and future research in biostatistics and biopharmaceuticals. The theme of this conference was Statistics for a New Generation: Challenges and Opportunities, in recognition of the advent of a new generation of statisticians. The conference attracted statisticians working in academia, government, and industry; domestic and international statisticians. From the conference, the editors selected 28 high-quality presentations and invited the speakers to prepare full chapters for this book. These contributions are divided into four parts: Part I Biostatistical Methodology, Part II Statistical Genetics and Bioinformatics, Part III Regulatory Statistics, and Part IV Biopharmaceutical Research and Applications.

Featuring contributions on topics such as statistics in genetics, bioinformatics, biostatistical methodology, and statistical computing, this book is beneficial to researchers, academics, practitioners and policy makers in biostatistics and biopharmaceuticals.

Similar content being viewed by others

Statistical Practices of Safety Monitoring: An Industry Survey

Article 01 May 2019

Introduction to Nonclinical Statistics for Pharmaceutical and Biotechnology Industries

Chapter © 2016

Using Bayesian statistics in confirmatory clinical trials in the regulatory setting: a tutorial review

Article Open access 07 May 2024

Keywords

Table of contents (18 chapters)

Front Matter

Biostatistical Methodology

Front Matter

Nonparametric Inference on Tumor Incidence with Partially Identified Cause-of-Death Data

Variable Selection for High Dimensional Metagenomic Data

Pages 19-32

Dimension Reduction in High Dimensional Multivariate Time Series Analysis

Pages 33-59

A Powerful Retrospective Multiple Variant Association Test for Quantitative Traits by Borrowing Strength from Complex Genotypic Correlations

Pages 61-90

Inference of Gene Regulatory Network Through Adaptive Dynamic Bayesian Network Modeling

Pages 91-113

Maximin Designs for Ultra-Fast Functional Brain Imaging

Pages 115-128

A Global Optimization Algorithm for Sparse Mixed Membership Matrix Factorization

Pages 129-156

A Nonnegative Robust Linear Model for Deconvolution of Proportions

Pages 157-165

Practical Design Approaches for Assessing Parallelism in Dose Response Modelling

Pages 167-181

Biopharmaceutical Applications

Front Matter

Pages 183-183

Optimal Adaptive Phase III Design with Interim Sample Size and Dose Determination

Pages 185-203

Critical Boundary Refinement in a Group Sequential Trial When the Primary Endpoint Data Accumulate Faster Than the Secondary Endpoint

Pages 205-224

Bayesian Dose Escalation Study Design with Consideration of Both Early and Late Onset Toxicity

Pages 225-238

A Bayesian Constancy-Enforced Non-Inferiority Design in Medical Device Trials with a Binary Endpoint

Pages 239-249

Adaptive Randomization for Master Protocols in Precision Medicine

Pages 251-270

Some Statistical Considerations in Design and Analysis for Nonrandomized Comparative Studies Using Existing Data as Controls for Medical Device Premarket Evaluation

Pages 271-284

Review of Statistical Issues in Pragmatic Clinical Trials in Current Drug Development Environment

Pages 285-298

Evaluating Potential Subpopulations Using Stochastic SIDEScreen in a Cross-Over Trial

Pages 299-322

Editors and Affiliations

Data and Statistical Sciences, AbbVie Inc., North Chicago, USA

School of Social Work, University of North Carolina, Chapel Hill, USA

Department of Statistics, Northwestern University, Evanston, USA

R&D, Janssen Pharmaceuticals, Raritan, USA

Sanofi US, Bridgewater, USA

About the editors

About the Editors:

Lanju Zhang is Director in Statistics and Research Fellow at the Department of Data and Statistical Sciences at AbbVie. He is leading a group providing statistical support to emerging immunology clinical programs. Prior to that, he was Head of Nonclinical Statistical Group at Abbvie and MedImmune. His research interests include adaptive design, multi-region clinical trials, real world evidence, and nonclinical statistics. He has published two books (both with Springer) and more than 30 papers. He is an associate editor of Journal of Biopharmaceutical Statistics. He received his PhD in Statistics in 2005 from University of Maryland Baltimore County.

Ding-Geng Chen is a Fellow of American Statistical Association and currently the Wallace H. Kuralt Distinguished Professor at the University of North Carolina at Chapel Hill. He was a professor at the University of Rochester and the Karl E. Peace Endowed Eminent Scholar Chairin Biostatistics at Georgia Southern University. He is also a senior statistics consultant for biopharmaceuticals and government agencies with extensive expertise in Monte-Carlo simulations, clinical trial biostatistics and public health statistics. Professor Chen has more than 150 referred professional publications and co-authored and co-edited 18 books on clinical trial methodology, meta-analysis and public health applications and he has been invited nationally and internationally to give speeches on his research.

Hongmei Jiang is an associate professor of statistics at Northwestern University. Her current research focuses on developing statistical methods and computational algorithms to analyze and understand the massive amount of data generated by high throughput biological technologies, such as microarray and next generation sequencing technologies. She has published over 40 research articles in statistics and biostatistics research fields. She was the Co-Chair for the 26th ICSA Applied Statistics Symposium, which was successfully held in Chicago in June 2017.

Gang Li is a scientific director, RWE Analytics at Janssen R&D US. He is an elected fellow of the American Statistical Association. Dr. Li received his PhD from the State University of New York at Binghamton. Gang has genuine interest in statistical research and has published a number of papers on multi-regional clinical trials, adaptive design and dose finding, and non-inferiority study design in leading statistical journals.

Hui Quan received his PhD in statistics from Columbia University in 1990. He is currently an associate VP and global head of the methodology group at the Biostatistics and Programming Department of Sanofi. He has 26 years of pharmaceutical industry experience in many therapeutic areas ranging from early phase to Phase IV studies. He has published 93 papers including 69 statistical papers. He is a co-author/co-editor of two books. He has also served as an associate editor for two journals. His research interests include multivariate analysis, safety analysis, multiplicity adjustment, missing data handling, adaptive design, integrated data analysis, modeling and simulation, benefit/risk assessment and multi-regional clinical trials. He was elected as a fellow of the American Statistical Association in 2008.

Bibliographic Information