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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
Edition:
illustrated
Number of Pages:
618
Release Date:
2009-04-22
Publication Date:
2009-04-23
Publisher:
Chapman and Hall/CRC
Languages:
Original: English
ISBN10:
1420066390
ISBN13:
9781420066395
Weight:
1083 g
Height:
161 cm
Width:
240 cm
Thickness:
37 cm
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