Adaptive Clinical Trials: Overview of Phase III Designs and Challenges
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[1] M A Proschan,et al. Designed extension of studies based on conditional power. , 1995, Biometrics.
[2] Frank Bretz,et al. Confirmatory adaptive designs with Bayesian decision tools for a targeted therapy in oncology , 2009, Statistics in medicine.
[3] Cyrus R Mehta,et al. Adaptive increase in sample size when interim results are promising: A practical guide with examples , 2011, Statistics in medicine.
[4] M Kieser,et al. Combining different phases in the development of medical treatments within a single trial. , 1999, Statistics in medicine.
[5] Sue-Jane Wang,et al. Modification of Sample Size in Group Sequential Clinical Trials , 1999, Biometrics.
[6] P. Bauer,et al. Evaluation of experiments with adaptive interim analyses. , 1994, Biometrics.
[7] Gernot Wassmer,et al. Designing Issues in Confirmatory Adaptive Population Enrichment Trials , 2015, Journal of Biopharmaceutical Statistics.
[8] Pascale Tubert-Bitter,et al. Targeting population entering phase III trials: A new stratified adaptive phase II design , 2011, Statistics in medicine.
[9] T. Friede,et al. A conditional error function approach for subgroup selection in adaptive clinical trials , 2012, Statistics in medicine.
[10] Mark C. K. Yang,et al. Interval estimation for drop-the-losers designs , 2010 .
[11] P. O'Brien,et al. A multiple testing procedure for clinical trials. , 1979, Biometrics.
[12] P. Gallo. Confidentiality and Trial Integrity Issues for Adaptive Designs , 2006 .
[13] C. Tournoux-Facon,et al. How a new stratified adaptive phase II design could improve targeting population , 2011, Statistics in medicine.
[14] Christopher Jennison,et al. Mid‐course sample size modification in clinical trials based on the observed treatment effect , 2002, Statistics in medicine.
[15] Jack Bowden,et al. Unbiased Estimation of Selected Treatment Means in Two‐Stage Trials , 2008, Biometrical journal. Biometrische Zeitschrift.
[16] Donald A. Berry,et al. Good Practices for Adaptive Clinical Trials in Pharmaceutical Product Development , 2009 .
[17] Sue-Jane Wang,et al. Approaches to evaluation of treatment effect in randomized clinical trials with genomic subset , 2007, Pharmaceutical statistics.
[18] R. Simon,et al. On the efficiency of targeted clinical trials , 2005, Statistics in medicine.
[19] R. Temple,et al. Enrichment designs: efficiency in development of cancer treatments. , 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[20] Frank Bretz,et al. Confirmatory Seamless Phase II/III Clinical Trials with Hypotheses Selection at Interim: General Concepts , 2006, Biometrical journal. Biometrische Zeitschrift.
[21] S. Pocock. Group sequential methods in the design and analysis of clinical trials , 1977 .
[22] Meinhard Kieser,et al. Simple procedures for blinded sample size adjustment that do not affect the type I error rate , 2003, Statistics in medicine.
[23] W. Lehmacher,et al. Adaptive Sample Size Calculations in Group Sequential Trials , 1999, Biometrics.
[24] C. Mehta,et al. Population Enrichment Designs: Case Study of a Large Multinational Trial , 2011, Journal of biopharmaceutical statistics.
[25] Gernot Wassmer,et al. On Sample Size Determination in Multi-Armed Confirmatory Adaptive Designs , 2011, Journal of biopharmaceutical statistics.
[26] Werner Brannath,et al. Shrinkage estimation in two‐stage adaptive designs with midtrial treatment selection , 2013, Statistics in medicine.
[27] Frank Bretz,et al. TUTORIAL IN BIOSTATISTICS Adaptive designs for confirmatory clinical trials , 2022 .
[28] Vladimir Dragalin,et al. Likelihood inference for a two‐stage design with treatment selection , 2010, Biometrical journal. Biometrische Zeitschrift.
[29] H. Magnussen,et al. Integrating Indacaterol Dose Selection in a Clinical Study in COPD Using an Adaptive Seamless Design. , 2009, ATS 2009.
[30] Jeff Maca,et al. Adaptive Seamless Phase II/III Designs—Background, Operational Aspects, and Examples , 2006 .
[31] A. Tsiatis,et al. On the inefficiency of the adaptive design for monitoring clinical trials , 2003 .
[32] D. DeMets,et al. Increasing the sample size when the unblinded interim result is promising , 2004, Statistics in medicine.
[33] Richard Simon,et al. Evaluation of randomized discontinuation design. , 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[34] R. Simon,et al. An agenda for Clinical Trials: clinical trials in the genomic era , 2004, Clinical trials.
[35] Martin Posch,et al. Testing and estimation in flexible group sequential designs with adaptive treatment selection , 2005, Statistics in medicine.
[36] C. Jennison,et al. An adaptive seamless phase II/III design for oncology trials with subpopulation selection using correlated survival endpoints † , 2011, Pharmaceutical statistics.
[37] Sue-Jane Wang,et al. Adaptive patient enrichment designs in therapeutic trials , 2009, Biometrical journal. Biometrische Zeitschrift.
[38] K. K. Lan,et al. Discrete sequential boundaries for clinical trials , 1983 .
[39] Cyrus Mehta,et al. Optimizing Trial Design: Sequential, Adaptive, and Enrichment Strategies , 2009, Circulation.