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is important to determine this quickly and terminate the clinical evaluation process to avoid wasting resources. Bayesian Designs for Phase I-II;
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is important to determine this quickly and terminate the clinical evaluation process to avoid wasting resources. Bayesian Designs for Phase I-II;
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computational tools needed for Bayesian clinical trials. With a focus on Bayesian designs that achieve good power and Type I error, the next chapters;
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properties, and operating characteristics for phase I, II, and III clinical trials as well as an introduction to phase IV trials. Many practical;
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finding in early phase clinical trials, the book then provides traditional and recent dose-finding designs of phase I trials for, e.g., cytotoxic;
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group sequential design, classical design, dose-finding trials, Phase III and Phase II/III seamless adaptive designs, multiple stage seamless;
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group sequential design, classical design, dose-finding trials, Phase III and Phase II/III seamless adaptive designs, multiple stage seamless;
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developments involved in the design and analysis of cancer clinical trials, incorporating updates to all four parts: Phase I trials;
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developments involved in the design and analysis of cancer clinical trials, incorporating updates to all four parts: Phase I trials;
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clinical trials still use single-arm designs. The book then presents methods for randomized phase II trials and describes statistical methods for;
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phase II trials since some methodologies for randomized phase II trials stem from single-arm phase II trials and many phase II cancer clinical;
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discussions on general clinical trials issues, and issues specific to Phases I, II, and III. New sections cover innovations in Phase I designs;
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discussions on general clinical trials issues, and issues specific to Phases I, II, and III. New sections cover innovations in Phase I designs;
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regarding phase II trial designs, A Practical Guide to Designing Phase II Trials in Oncology sets forth specific points for consideration between;
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designs, including novel Bayesian strategies for dose escalation. This volume is designed to help clinicians better understand phase I;
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study designs and their applications to different therapeutic areas. Clinical Trials in Neurology covers key issues in Phase I, II and III;
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circumstances? What special considerations are required for adaptive randomized trials? What kind of statistical inference should be used to achieve;
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guide for statisticians and investigators with minimal clinical trial experience who are interested in pursuing a career in this area. The;
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guide for statisticians and investigators with minimal clinical trial experience who are interested in pursuing a career in this area. The;
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: Classical, Adaptive, and Bayesian Methods, edited by Sandeep M. Menon and Richard C. Zink, thoroughly covers several domains of modern clinical;
Vergelijkbare producten zoals Modern Approaches to Clinical Trials Using SAS
: Classical, Adaptive, and Bayesian Methods, edited by Sandeep M. Menon and Richard C. Zink, thoroughly covers several domains of modern clinical;
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This book deals with advanced methods for adaptive phase I dose-finding clinical trials for combination of two agents and molecularly;
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Clinical trials are used to elucidate the most appropriate preventive, diagnostic, or treatment options for individuals with a given;
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in Phase II clinical trials. He is one of the co-developers of the MCP-Mod methodology for dose finding and main author of the DoseFinding R;
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Single-Arm Phase II Survival Trial Design provides a comprehensive summary to the most commonly- used methods for single-arm phase II trial;
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A complete guide to the key statistical concepts essential for the design and construction of clinical trials As the newest major resource;
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of Phase III Clinical Drug Trials is that source. It is an indispensable guide, readily providing the information needed to make crucial decisions;
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