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Biopharmaceutical Applied Statistics Symposium - Volume 1 Design of Clinical Trials (Hardcover, 1st ed. 2018)
Loot Price: R2,856
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Biopharmaceutical Applied Statistics Symposium - Volume 1 Design of Clinical Trials (Hardcover, 1st ed. 2018)
Series: ICSA Book Series in Statistics
Expected to ship within 10 - 15 working days
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This BASS book Series publishes selected high-quality papers
reflecting recent advances in the design and biostatistical
analysis of biopharmaceutical experiments - particularly
biopharmaceutical clinical trials. The papers were selected from
invited presentations at the Biopharmaceutical Applied Statistics
Symposium (BASS), which was founded by the first Editor in 1994 and
has since become the premier international conference in
biopharmaceutical statistics. The primary aims of the BASS are: 1)
to raise funding to support graduate students in biostatistics
programs, and 2) to provide an opportunity for professionals
engaged in pharmaceutical drug research and development to share
insights into solving the problems they encounter.The BASS book
series is initially divided into three volumes addressing: 1)
Design of Clinical Trials; 2) Biostatistical Analysis of Clinical
Trials; and 3) Pharmaceutical Applications. This book is the first
of the 3-volume book series. The topics covered include: A
Statistical Approach to Clinical Trial Simulations, Comparison of
Statistical Analysis Methods Using Modeling and Simulation for
Optimal Protocol Design, Adaptive Trial Design in Clinical
Research, Best Practices and Recommendations for Trial Simulations
in the Context of Designing Adaptive Clinical Trials, Designing and
Analyzing Recurrent Event Data Trials, Bayesian Methodologies for
Response-Adaptive Allocation, Addressing High Placebo Response in
Neuroscience Clinical Trials, Phase I Cancer Clinical Trial Design:
Single and Combination Agents, Sample Size and Power for the Mixed
Linear Model, Crossover Designs in Clinical Trials, Data
Monitoring: Structure for Clinical Trials and Sequential Monitoring
Procedures, Design and Data Analysis for Multiregional Clinical
Trials - Theory and Practice, Adaptive Group-Sequential
Multi-regional Outcome Studies in Vaccines, Development and
Validation of Patient-reported Outcomes, Interim Analysis of
Survival Trials: Group Sequential Analyses, and Conditional Power -
A Non-proportional Hazards Perspective.
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