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Design and analysis of bridging studies

Contributor(s): Liu, Jen-pei [Editor] | Chow, Shein-Chung [Editor] | Hsiao, Chin-Fu [Editor].
Series: Chapman & Hall/CRC Biostatistics Series. Publisher: Boca Raton CRC Press 2013Description: xviii, 269 p.ISBN: 9781439846346.Subject(s): Drugs - Testing - Standards | Clinical trials - Standards | Biometry - Methodology | Clinical Trials as Topic - Standards | Biostatistics - Methods | Internationality | Drug development - Statistical methodsDDC classification: 615.10724 Summary: As the development of medicines has become more globalized, the geographic variations in the efficacy and safety of pharmaceutical products need to be addressed. To accelerate the product development process and shorten approval time, researchers are beginning to design multiregional trials that incorporate subjects from many countries around the world under the same protocol. Design and Analysis of Bridging Studies addresses the issues arising from bridging studies and multiregional clinical trials. For bridging studies, the book explores ethnic sensitivity, the necessity of bridging studies, types of bridging studies, and the assessment of similarity between regions based on bridging evidence. For multiregional clinical trials, the text considers regional differences, assesses the consistency of treatment effect across regions, and discusses sample size determination for each region. Taking into account the International Conference Harmonisation (ICH) E5 framework for bridging studies, the book provides a unified summary of the growing literature and research activities in this area. It covers the regulatory requirements, scientific and practical issues, and statistical methodology for designing and evaluating bridging studies and multiregional clinical trials, with the goal of inspiring new research activities in the field. (https://www.crcpress.com/Design-and-Analysis-of-Bridging-Studies/Liu-Chow-Hsiao/p/book/9781439846346)
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Slot 1733 (2 Floor, East Wing) Non-fiction 615.10724 D3 (Browse shelf) Available 192557

Table of Contents:

1.Bridging Diversity: Extrapolating Foreign Data to a New Region

2.Two-Stage Designs of Bridging Studies

3.Consistency of Treatment Effects in Bridging Studies and Global Multiregional Trials

4.Assessing Similarity Using the Reproducibility and Generalizability Probabilities and the Sensitivity Index

5.Combining Information in Clinical Drug Development: Bridging Studies and Beyond

6.A Bayesian Approach for Evaluation of Bridging Studies

7.Issues of Sample Size in Bridging Trials and Global Clinical Trials

8.Design and Sample Size Considerations for Global Trials

9.Application of Genomic Technologies for Bridging Strategy Involving Different Race and Ethnicity in Pharmacogenomics Clinical Trials

10.Interaction Effects in Bridging Studies

11.Multiregional Clinical Trials

12.Multiregional Clinical Trials for Global Simultaneous Drug Development in Japan

13.Feasibility and Implementation of Bridging Studies in Taiwan

Index

As the development of medicines has become more globalized, the geographic variations in the efficacy and safety of pharmaceutical products need to be addressed. To accelerate the product development process and shorten approval time, researchers are beginning to design multiregional trials that incorporate subjects from many countries around the world under the same protocol.

Design and Analysis of Bridging Studies addresses the issues arising from bridging studies and multiregional clinical trials. For bridging studies, the book explores ethnic sensitivity, the necessity of bridging studies, types of bridging studies, and the assessment of similarity between regions based on bridging evidence. For multiregional clinical trials, the text considers regional differences, assesses the consistency of treatment effect across regions, and discusses sample size determination for each region.

Taking into account the International Conference Harmonisation (ICH) E5 framework for bridging studies, the book provides a unified summary of the growing literature and research activities in this area. It covers the regulatory requirements, scientific and practical issues, and statistical methodology for designing and evaluating bridging studies and multiregional clinical trials, with the goal of inspiring new research activities in the field.

(https://www.crcpress.com/Design-and-Analysis-of-Bridging-Studies/Liu-Chow-Hsiao/p/book/9781439846346)

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