Flexible Interim Analyses in Clinical Trials Using Multistage Adaptive Test Designs
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[1] J. Wittes,et al. The role of internal pilot studies in increasing the efficiency of clinical trials. , 1990, Statistics in medicine.
[2] M A Proschan,et al. Designed extension of studies based on conditional power. , 1995, Biometrics.
[3] L E Braitman. Statistical estimates and clinical trials. , 1993, Journal of biopharmaceutical statistics.
[4] L Fisher,et al. Statistical Inference for Self‐Designing Clinical Trials with a One‐Sided Hypothesis , 1999, Biometrics.
[5] R. Kay. Statistical Principles for Clinical Trials , 1998, The Journal of international medical research.
[6] J. Wittes,et al. The Use of Interim Analysis for Sample Size Adjustment , 1993 .
[7] T M Therneau,et al. Designs for group sequential phase II clinical trials. , 1987, Biometrics.
[8] T. Fleming,et al. Parameter estimation following group sequential hypothesis testing , 1990 .
[9] G Y Chi,et al. The attractiveness of the concept of a prospectively designed two-stage clinical trial. , 1999, Journal of biopharmaceutical statistics.
[10] A. Tsiatis,et al. Approximately optimal one-parameter boundaries for group sequential trials. , 1987, Biometrics.
[11] A. Gould. Planning and revising the sample size for a trial. , 1995, Statistics in Medicine.
[12] H. Schäfer,et al. Adaptive Group Sequential Designs for Clinical Trials: Combining the Advantages of Adaptive and of Classical Group Sequential Approaches , 2001, Biometrics.
[13] Gernot Wassmer,et al. Multistage Adaptive Test Procedures Based on Fisher's Product Criterion , 1999 .
[14] M Kieser,et al. Combining different phases in the development of medical treatments within a single trial. , 1999, Statistics in medicine.
[15] Christopher Jennison,et al. Interim analyses: the repeated confidence interval approach , 1989 .
[16] Alan Phillips,et al. The International Conference on Harmonization Guideline “Statistical Principles for Clinical Trials”: Issues in Applying the Guideline in Practice , 2000 .
[17] B. Turnbull,et al. Group Sequential Methods with Applications to Clinical Trials , 1999 .
[18] L. Braitman,et al. Satistical estimates and clinical trials , 1993 .
[19] W. Lehmacher,et al. Sequential and Multiple Testing for Dose-Response Analysis , 2000 .
[20] Z. Shun,et al. Type I error in sample size re‐estimations based on observed treatment difference , 2001, Statistics in medicine.
[21] J Röhmel,et al. An adaptive method for establishing a dose-response relationship. , 1995, Statistics in medicine.
[22] David L. DeMets,et al. Estimating and reducing bias in group sequential designs with Gaussian independent increment structure , 1997 .
[23] G. Chi,et al. On Sample Size and Inference for Two‐Stage Adaptive Designs , 2001, Biometrics.
[24] K Kim,et al. Point estimation following group sequential tests. , 1989, Biometrics.
[25] Sue-Jane Wang,et al. Modification of Sample Size in Group Sequential Clinical Trials , 1999, Biometrics.
[26] M A Proschan,et al. An improved double sampling procedure based on the variance. , 2000, Biometrics.
[27] B. K. Ghosh,et al. Handbook of sequential analysis , 1991 .
[28] S J Pocock,et al. Interim analyses for randomized clinical trials: the group sequential approach. , 1982, Biometrics.
[29] Christopher Jennison,et al. Exact calculations for sequential t, X2 and F tests , 1991 .
[30] C. Jennison,et al. Group Sequential tests and Repeated Confidence Intervals , 1988 .
[31] S S Emerson. Computation of the uniform minimum variance unbiased estimator of a normal mean following a group sequential trial. , 1993, Computers and biomedical research, an international journal.
[32] David L. DeMets,et al. Group sequential methods for clinical trials with a one-sided hypothesis , 1980 .
[33] S. Day,et al. Internal pilot studies for estimating sample size. , 1994, Statistics in medicine.
[34] W. J. Hall,et al. Unbiased estimation following a group sequential test , 1999 .
[35] K McPherson. On choosing the number of interim analyses in clinical trials. , 1982, Statistics in medicine.
[36] J. Denne,et al. ESTIMATION FOLLOWING EXTENSION OF A STUDY ON THE BASIS OF CONDITIONAL POWER , 2000, Journal of biopharmaceutical statistics.
[37] W. Lehmacher,et al. Adaptive Sample Size Calculations in Group Sequential Trials , 1999, Biometrics.
[38] David L. DeMets,et al. Asymmetric group sequential boundaries for monitoring clinical trials , 1982 .
[39] S. Pocock. Group sequential methods in the design and analysis of clinical trials , 1977 .
[40] P Bauer,et al. Interim Analysis and Sample Size Reassessment , 2000, Biometrics.
[41] T R Fleming,et al. Designs for group sequential tests. , 1984, Controlled clinical trials.
[42] Meinhard Kieser,et al. Inference on Multiple Endpoints in Clinical Trials with Adaptive Interim Analyses , 1999 .
[43] P. O'Brien,et al. A multiple testing procedure for clinical trials. , 1979, Biometrics.
[44] Meinhard Kieser,et al. Blinded Sample Size Reestimation in Multiarmed Clinical Trials , 2000 .
[45] L D Fisher,et al. Self-designing clinical trials. , 1998, Statistics in medicine.
[46] T. Friede,et al. Re-calculating the sample size in internal pilot study designs with control of the type I error rate. , 2000, Statistics in medicine.
[47] John Whitehead,et al. On the bias of maximum likelihood estimation following a sequential test , 1986 .
[48] A L Gould,et al. Interim analyses for monitoring clinical trials that do not materially affect the type I error rate. , 1992, Statistics in medicine.
[49] P Bauer,et al. Flexible Two-Stage Designs: An Overview , 2001, Methods of Information in Medicine.
[50] M. Hellmich. Monitoring Clinical Trials with Multiple Arms , 2001, Biometrics.
[51] S. Emerson,et al. A computationally simpler algorithm for the UMVUE of a normal mean following a group sequential trial. , 1997, Biometrics.
[52] P. Bauer,et al. Trendtests with adaptive scoring , 2000 .
[53] G. Hommel,et al. Multiple Comparisons of Treatments with Stable Multivariate Tests in a Two‐Stage Adaptive Design, Including a Test for Non‐Inferiority , 2000 .
[54] Gernot Wassmer,et al. Basic concepts of group sequential and adaptive group sequential test procedures , 2000 .
[55] Lakhbir S. Hayre. Group Sequential Sampling with Variable Group Sizes , 1985 .
[56] Michael A. Proschan,et al. Effects of assumption violations on type I error rate in group sequential monitoring , 1992 .
[57] Gernot Wassmer,et al. A Technical Note on the Power Determination for Fisher's Combination Test , 1997 .
[58] K. K. Lan,et al. Discrete sequential boundaries for clinical trials , 1983 .
[59] HansâHelge Müller,et al. Adaptive Group Sequential Designs for Clinical Trials: Combining the Advantages of Adaptive and of Classical Group Sequential Approaches , 2001 .
[60] L. Hedges,et al. Statistical Methods for Meta-Analysis , 1987 .
[61] P. Bauer,et al. Evaluation of experiments with adaptive interim analyses. , 1994, Biometrics.
[62] G. Hommel. Adaptive Modifications of Hypotheses After an Interim Analysis , 2001 .
[63] M. Proschan,et al. Internal pilot studies I: type I error rate of the naive t-test. , 1999, Statistics in medicine.
[64] T. Friede,et al. A comparison of methods for adaptive sample size adjustment , 2001, Statistics in medicine.
[65] M. Neuhäuser. An Adaptive Location-Scale Test , 2001 .
[66] G Wassmer,et al. A comparison of two methods for adaptive interim analyses in clinical trials. , 1998, Biometrics.
[67] Gernot Wassmer,et al. Conditional Point Estimation in Adaptive Group Sequential Test Designs , 2001 .
[68] D. Zucker,et al. Internal pilot studies II: comparison of various procedures. , 1999, Statistics in medicine.
[69] P. Bauer,et al. Adaptive Two Stage Designs and the Conditional Error Function , 1999 .