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Multiple Analyses in Clinical Trials, Lemuel A. Moy?


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Автор: Lemuel A. Moy?
Название:  Multiple Analyses in Clinical Trials
ISBN: 9781441918369
Издательство: Springer
Классификация:

ISBN-10: 1441918361
Обложка/Формат: Paperback
Страницы: 436
Вес: 0.64 кг.
Дата издания: 29.11.2010
Серия: Statistics for Biology and Health
Язык: English
Размер: 234 x 156 x 24
Основная тема: Biomedicine
Подзаголовок: Fundamentals for Investigators
Ссылка на Издательство: Link
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Поставляется из: Германии
Описание: One of the most challenging issues for clinical trial investigators, sponsors, and regulatory officials is the interpretation of experimental results that are composed of the results of multiple statistical analyses. These analyses may include the effect of therapy on multiple endpoints, the assessment of a subgroup analysis, and the evaluation of a dose-response relationship in complex mixtures. Multiple Analyses in Clinical Trials: Fundamentals for Clinical Investigators is an essentially nonmathematical discussion of the problems posed by the execution of multiple analyses in clinical trials. It concentrates on the rationale for the analyses, the difficulties posed by their interpretation, easily understood solutions, and useful problem sets. This text will help clinical investigators understand multiple analysis procedures and the key issues when designing their own work or reviewing the research of others. This book is written for advanced medical students, clinical investigators at all levels, research groups within the pharmaceutical industry, regulators at the local, state, and federal level, and biostatisticians. Only a basic background in health care and introductory statistics is required. Dr. Lemuel A. Moye, M.D., Ph.D. is a physician and Professor of Biometry at the University of Texas School of Public Health. He has been Co-Principal Investigator of two multinational clinical trials examining the role of innovative therapy in post myocardial infarction survival (SAVE) and the use of cholesterol reducing agents in post myocardial infarction survival in patients with normal cholesterol levels (CARE). He has authored over one hundred articles in journals such as the Journal of the American Medical Association, the New England Journal of Medicine, Statistics in Medicine, and Controlled Clinical Trials.


Fundamentals of Clinical Trials

Автор: Lawrence M. Friedman; Curt D. Furberg; David L. De
Название: Fundamentals of Clinical Trials
ISBN: 3319307738 ISBN-13(EAN): 9783319307732
Издательство: Springer
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Цена: 6986.00 р.
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Описание: This is the fifth edition of a very successful textbook on clinical trials methodology, written by recognized leaders who have long and extensive experience in all areas of clinical trials. The three authors of the first four editions have been joined by two others who add great expertise. A chapter on regulatory issues has been included and the chapter on data monitoring has been split into two and expanded. Many contemporary clinical trial examples have been added. There is much new material on adverse events, adherence, issues in analysis, electronic data, data sharing and international trials. This book is intended for the clinical researcher who is interested in designing a clinical trial and developing a protocol. It is also of value to researchers and practitioners who must critically evaluate the literature of published clinical trials and assess the merits of each trial and the implications for the care and treatment of patients. The authors use numerous examples of published clinical trials to illustrate the fundamentals. The text is organized sequentially from defining the question to trial closeout. One chapter is devoted to each of the critical areas to aid the clinical trial researcher. These areas include pre-specifying the scientific questions to be tested and appropriate outcome measures, determining the organizational structure, estimating an adequate sample size, specifying the randomization procedure, implementing the intervention and visit schedules for participant evaluation, establishing an interim data and safety monitoring plan, detailing the final analysis plan and reporting the trial results according to the pre-specified objectives. Although a basic introductory statistics course is helpful in maximizing the benefit of this book, a researcher or practitioner with limited statistical background would still find most if not all the chapters understandable and helpful. While the technical material has been kept to a minimum, the statistician may still find the principles and fundamentals presented in this text useful.

Sample Size Determination in Clinical Trials with Multiple Endpoints

Автор: Takashi Sozu; Tomoyuki Sugimoto; Toshimitsu Hamasa
Название: Sample Size Determination in Clinical Trials with Multiple Endpoints
ISBN: 3319220047 ISBN-13(EAN): 9783319220048
Издательство: Springer
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Цена: 6986.00 р.
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Описание:

1.Introduction.- 2.Continuous Co-primary Endpoints.- 3.Binary Co-primary Endpoints.- 4.Convenient Sample Size Formula.- 5.Continuous Primary Endpoints.- 6. Further Developments.- A.Sample Size Calculation Using other Contrasts for Binary Endpoints.- B.Empirical Power for Sample Size Calculation for Binary Co-primary Endpoints.- C.Numerical Tables for Ck in the Convenient Sample Size Formula for the Three Co-primary Continuous Endpoints Cace.- D.Software Programs for Sample Size Calculation for Continuous Co-primary Endpoints.- References.

Cancer Clinical Trials

Автор: Hans Scheurlen; Richard Kay; Michael Baum
Название: Cancer Clinical Trials
ISBN: 3642834213 ISBN-13(EAN): 9783642834219
Издательство: Springer
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Цена: 18167.00 р.
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Описание: The meeting was generously supported again by the Federal Ministry of Research and Technology (Bundesministe rium flir Forschung und Technologie, BMFT) within the framework of the West German BMFT Breast Cancer Study Group.

Optimized Response-Adaptive Clinical Trials

Автор: Thomas Ondra
Название: Optimized Response-Adaptive Clinical Trials
ISBN: 3658083433 ISBN-13(EAN): 9783658083434
Издательство: Springer
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Цена: 9141.00 р.
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Описание: Two-armed response-adaptive clinical trials are modelled as Markov decision problems to pursue two overriding objectives: Firstly, to identify the superior treatment at the end of the trial and, secondly, to keep the number of patients receiving the inferior treatment small.

Statistical Applications from Clinical Trials and Personalized Medicine to Finance and Business Analytics

Автор: Lin
Название: Statistical Applications from Clinical Trials and Personalized Medicine to Finance and Business Analytics
ISBN: 3319425676 ISBN-13(EAN): 9783319425672
Издательство: Springer
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Цена: 20263.00 р.
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Описание:

The papers in this volume represent a broad, applied swath of advanced contributions to the 2015 ICSA/Graybill Applied Statistics Symposium of the International Chinese Statistical Association, held at Colorado State University in Fort Collins. The contributions cover topics that range from statistical applications in business and finance to applications in clinical trials and biomarker analysis. Each papers was peer-reviewed by at least two referees and also by an editor. The conference was attended by over 400 participants from academia, industry, and government agencies around the world, including from North America, Asia, and Europe.
Applied Statistics in Biomedicine and Clinical Trials Design

Автор: Zhen Chen; Aiyi Liu; Yongming Qu; Larry Tang; Nait
Название: Applied Statistics in Biomedicine and Clinical Trials Design
ISBN: 3319126938 ISBN-13(EAN): 9783319126937
Издательство: Springer
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Цена: 26552.00 р.
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Описание: The peer-reviewed contributions were solicited and selected from some 400 presentations at the annual meeting of the International Chinese Statistical Association (ICSA), held with the International Society for Biopharmaceutical Statistics (ISBS).

Statistics in Clinical Vaccine Trials

Автор: Jozef Nauta
Название: Statistics in Clinical Vaccine Trials
ISBN: 3642441912 ISBN-13(EAN): 9783642441912
Издательство: Springer
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Цена: 14673.00 р.
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Описание: This book offers training and expertise on the statistical analysis of data from clinical vaccine trials, i.e., immunogenicity and vaccine field efficacy studies. With many worked-out real-life examples, its scope is more practical than theoretical.

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

Автор: Takashi Daimon; Akihiro Hirakawa; Shigeyuki Matsui
Название: An Introduction to Dose-Finding Methods in Early Phase Clinical Trials
ISBN: 4431555846 ISBN-13(EAN): 9784431555841
Издательство: Springer
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Цена: 6986.00 р.
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Описание: Included are rule-based and model-based designs, such as 3 + 3 designs, accelerated titration designs, toxicity probability interval designs, continual reassessment method and related designs, and escalation overdose control designs.


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