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Modern Dose Finding Designs for Cancer Phase I Trials Drug Combinations and Mol

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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An Introduction to Dose-Finding Methods in Early Phase Clinical Trials

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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Phase I Oncology Drug Development

in cancer drug development. It could also be of use to phase I trial study coordinators, oncology nurses and advanced practice providers. Other;

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Dose Finding by the Continual Reassessment Method

regular basis. A detailed exposition of the calibration of the CRM for applied statisticians working with dose-finding in phase I trials, the book;

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Novel Designs of Early Phase Trials for Cancer Therapeutics

a comprehensive review and recommendations for new clinical trial designs for modern cancer therapeutics Provides the reader with a;

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Handbook of Methods for Designing, Monitoring, and Analyzing DoseFinding Trials Chapman HallCRC Handbooks of Modern Statistical Methods

Handbook of Methods for Designing, Monitoring, and Analyzing Dose-Finding Trials gives a thorough presentation of state-of-the-art methods;

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Bayesian Designs for Phase I-II Clinical Trials

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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Bayesian Designs for Phase I II Clinical Trials

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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Statistical Methods for Dose-Finding Experiments

-finding in phase I/II clinical trials and presents practical guidance on their correct use. * Includes an introductory section, summarizing the;

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Handbook of Adaptive Designs in Pharmaceutical and Clinical Development

group sequential design, classical design, dose-finding trials, Phase I/II and Phase II/III seamless adaptive designs, multiple stage seamless;

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Handbook of Adaptive Designs in Pharmaceutical and Clinical Development

group sequential design, classical design, dose-finding trials, Phase I/II and Phase II/III seamless adaptive designs, multiple stage seamless;

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Clinical Trial Design

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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Handbook of Statistics in Clinical Oncology

developments involved in the design and analysis of cancer clinical trials, incorporating updates to all four parts: Phase I trials;

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Handbook of Statistics in Clinical Oncology

developments involved in the design and analysis of cancer clinical trials, incorporating updates to all four parts: Phase I trials;

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Randomized Phase II Cancer Clinical Trials

-arm phase II trials since some methodologies for randomized phase II trials stem from single-arm phase II trials and many phase II cancer;

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Randomized Phase II Cancer Clinical Trials

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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Kinase Inhibitor Drugs

Kinase Inhibitor Drugs covers a wide and comprehensive range of topics about kinase-targeted inhibitors in cancer therapy, one of the;

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Clinical Trials in Oncology

of methods and issues related to cancer clinical trials. The authors emphasize the importance of proper study design, analysis, and data management;

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Clinical Trials in Oncology, Third Edition

of methods and issues related to cancer clinical trials. The authors emphasize the importance of proper study design, analysis, and data management;

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Bioequivalence and Statistics in Clinical Pharmacology

, but are not limited to, safety studies in Phase I, dose-response trials, drug interaction trials, food-effect and combination trials, QTc and;

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Bioequivalence and Statistics in Clinical Pharmacology

, but are not limited to, safety studies in Phase I, dose-response trials, drug interaction trials, food-effect and combination trials, QTc and;

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Bioequivalence and Statistics in Clinical Pharmacology

in Phase I, dose-response trials, drug interaction trials, food-effect and combination trials, QTc and other pharmacodynamic equivalence trials;

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Bayesian Adaptive Methods for Clinical Trials

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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Drug Synergism and Dose-Effect Data Analysis

accompany a presentation that clearly illustrates the calculations and experimental design considerations for modern drug analysis. You'll find the;

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Drug Synergism and Dose-Effect Data Analysis

accompany a presentation that clearly illustrates the calculations and experimental design considerations for modern drug analysis. You'll find the;

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A Practical Guide to Designing Phase II Trials in Oncology

design phase II trials in cancer are given. A Practical Guide to Designing Phase II Trials in Oncology: * Offers a structured and practical;

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Modern Adaptive Randomized Clinical Trials

valid and unbiased treatment comparisons following adaptive randomization designs? Modern Adaptive Randomized Clinical Trials: Statistical and;

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