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Design and Analysis of Clinical Trials with Time-to-Event Endpoints

Design and Analysis of Clinical Trials with Time-to-Event Endpoints Medicine

Design and Analysis of Clinical Trials with Time-to-Event Endpoints

0 - Default Title
Description
This resource provides a thorough presentation of the design, monitoring, analysis, and interpretation of clinical trials in which time-to-event is of critical interest. Incorporating the collaborations of truly world-class statisticians, it discusses the design and monitoring of Phase II and III clinical trials with time-to-event endpoints. The book presents parametric, semiparametric, categorical, and Bayesian inferential and descriptive methods for analyzing time-to-event endpoints and covers numerous clinical trial applications, including analgesic, antibiotic, antiviral, cancer and cardiovascular prevention, optimal assignment of treatments, adverse events, and carcinogenicity.
Product details
Binding:
Paperback
Edition:
1
Number of Pages:
618
Release Date:
2018-09-10
Publication Date:
2018-09-10
Publisher:
Chapman and Hall/CRC
Languages:
Original: English
ISBN10:
1138372668
ISBN13:
9781138372665
GPSR Manufacturer Reference:
Weight:
925 g
Height:
156 cm
Width:
234 cm
Thickness:
33 cm
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