Design and Analysis of Group Sequential Clinical Trials with Multiple Primary Endpoints

DOI10.1111/J.0006-341X.2004.00146.XzbMATH Open1130.62374WikidataQ44806501 ScholiaQ44806501MaRDI QIDQ3435673FDOQ3435673

Authors: Michael R. Kosorok, Yuanjun Shi, David L. Demets 

Publication date: 7 May 2007

Published in: Biometrics (Search for Journal in Brave)

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zbMATH Keywords

time-to-event datasample sizemultivariate outcomesalpha-spending functionbeta-spending function

Mathematics Subject Classification ID

Applications of statistics to biology and medical sciences; meta analysis (62P10) Sequential statistical design (62L05)

Cites Work

• Title not available (Why is that?)
• Title not available (Why is that?)
• Repeated Significance Testing for a General Class of Statistics Used in Censored Survival Analysis
• Group sequential designs for one-sided and two-sided hypothesis testing with provision for early stopping in favor of the null hypothesis

Cited In (17)

• Closed Testing Procedures for Group Sequential Clinical Trials with Multiple Endpoints
• Non-parametric group sequential designs in randomized clinical trials
• A Geometric Approach to Comparing Treatments for Rapidly Fatal Diseases
• Longitudinal clinical trials with adaptive choice of follow-up time
• Interim evaluation of efficacy or futility in group‐sequential trials with multiple co‐primary endpoints
• BAGS: a Bayesian adaptive group sequential trial design with subgroup-specific survival comparisons
• Group-Sequential Clinical Trials with Multiple Co-Objectives
• A nonparametric test for the evaluation of group sequential clinical trials with covariate information
• Exact sequential analysis for multiple weighted binomial end points
• A Bayesian Group Sequential Approach for Multiple Endpoints
• Statistical monitoring of clinical trials with multivariate response and/or multiple arms: a flexible approach
• The simultaneous analysis of mixed discrete and continuous outcomes using nonlinear threshold models
• Evaluating co-primary endpoints collectively in clinical trials
• Testing a Primary and a Secondary Endpoint in a Group Sequential Design
• Multistage nonparametric tests for treatment comparisons in clinical trials with multiple primary endpoints
• Group-sequential logrank methods for trial designs using bivariate non-competing event-time outcomes
• Simultaneous population enrichment and endpoint selection in phase 3 randomized controlled trials: An adaptive group sequential design with two binary alternative primary endpoints

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