Biopharmaceutical Applied Statistics Symposium Volume 1 Design of Clinical Trials /

Biopharmaceutical Applied Statistics Symposium Volume 1 Design of Clinical Trials /

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 S...

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Bibliographic Details
Corporate Author: SpringerLink (Online service)
Other Authors: Peace, Karl E. (Editor, http://id.loc.gov/vocabulary/relators/edt), Chen, Ding-Geng (Editor, http://id.loc.gov/vocabulary/relators/edt), Menon, Sandeep (Editor, http://id.loc.gov/vocabulary/relators/edt)
Format: Electronic eBook
Language:English
Published: Singapore : Springer Singapore : Imprint: Springer, 2018.
Edition:1st ed. 2018.
Series:ICSA Book Series in Statistics,
Subjects:
Statistics .
Biostatistics.
Statistics for Life Sciences, Medicine, Health Sciences.
Online Access:Full Text via HEAL-Link
Table of Contents:
  • 1. A Statistical Approach to Clinical Trial Simulations
  • 2. Comparison of Statistical Analysis Methods Using Modeling and Simulation for Optimal Protocol Design
  • 3. Adaptive Trial Design in Clinical Research
  • 4. Best Practices and Recommendations for Trial Simulations Within the Context of Designing Adaptive Clinical Trials
  • 5. Designing and Analyzing Recurrent Event Data Trials
  • 6. Bayesian Methodologies for Response-Adaptive Allocation
  • 7. Addressing High Placebo Response in Neuroscience Clinical Trials
  • 8. Phase I Cancer Clinical Trial Design: Single and Combination Agents
  • 9. Sample Size and Power for the Mixed Linear Model
  • 10. Crossover Designs
  • 11. Data monitoring: Structure for Clinical Trials and Sequential Monitoring Procedures
  • 12. Design and Data Analysis of Multiregional Clinical Trials (MRCT) - Theory and Practice
  • 13. Multiregional Clinical Trials (MRCT)
  • 14. Adaptive Group-Sequential Multi-regional Outcome Studies in Vaccines
  • 15. Development and validation of Patient-reported Outcomes
  • 16. Interim Analysis of Survival Trials: Group Sequential Analyses and Conditional Power.

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