Princeton University Library Catalog

Clinical trial methodology / Karl E. Peace, Ding-Geng (Din) Chen.

Author:
Peace, Karl E., 1941- [Browse]
Format:
Book
Language:
English
Published/​Created:
Boca Raton : Chapman and Hall/CRC Press, c2011.
Description:
xxv, 394 p. : ill. ; 25 cm.
Series:
  • Chapman & Hall/CRC biostatistics series ; 35. [More in this series]
  • Chapman & Hall/CRC biostatistics series ; 35
Summary note:
"Now viewed as its own scientific discipline, clinical trial methodology encompasses the methods required for the protection of participants in a clinical trial and the methods necessary to provide a valid inference about the objective of the trial. Drawing from the authors courses on the subject as well as the first authors more than 30 years working in the pharmaceutical industry, Clinical trial methodology emphasizes the importance of statistical thinking in clinical research and presents the methodology as a key component of clinical research. From ethical issues and sample size considerations to adaptive design procedures and statistical analysis, the book first covers the methodology that spans every clinical trial regardless of the area of application. Crucial to the generic drug industry, bioequivalence clinical trials are then discussed. The authors describe a parallel bioequivalence clinical trial of six formulations incorporating group sequential procedures that permit sample size re-estimation. The final chapters incorporate real-world case studies of clinical trials from the authors own experiences. These examples include a landmark Phase III clinical trial involving the treatment of duodenal ulcers and Phase III clinical trials that contributed to the first drug approved for the treatment of Alzheimers disease. Aided by the U.S. FDA, the U.S. National Institutes of Health, the pharmaceutical industry, and academia, the area of clinical trial methodology has evolved over the last six decades into a scientific discipline. This guide explores the processes essential for developing and conducting a quality clinical trial protocol and providing quality data collection, biostatistical analyses, and a clinical study report, all while maintaining the highest standards of ethics and excellence"--Provided by publisher.
Bibliographic references:
Includes bibliographical references and index.
Subject(s):
ISBN:
  • 9781584889175 (hardcover : alk. paper)
  • 1584889179 (hardcover : alk. paper)
LCCN:
2010021864
OCLC:
632070587
Other standard number:
  • 40018182494
Related name:
RCP:
C - S