Adaptive clinical trial design.
暂无分享,去创建一个
[1] Michael Krams,et al. Implementing Adaptive Designs: Logistical and Operational Considerations , 2006 .
[2] Jeff Maca,et al. Adaptive Seamless Phase II/III Designs—Background, Operational Aspects, and Examples , 2006 .
[3] Richard Simon,et al. Two-stage selection and testing designs for comparative clinical trials , 1988 .
[4] B E Storer,et al. Design and analysis of phase I clinical trials. , 1989, Biometrics.
[5] D. Berry,et al. Adaptive assignment versus balanced randomization in clinical trials: a decision analysis. , 1995, Statistics in medicine.
[6] A. Gould,et al. Sample size re-estimation without unblinding for normally distributed outcomes with unknown variance , 1992 .
[7] Sue-Jane Wang,et al. Modification of Sample Size in Group Sequential Clinical Trials , 1999, Biometrics.
[8] Elizabeth Garrett-Mayer,et al. The continual reassessment method for dose-finding studies: a tutorial , 2006, Clinical trials.
[9] 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.
[10] Sue-Jane Wang,et al. Approaches to evaluation of treatment effect in randomized clinical trials with genomic subset , 2007, Pharmaceutical statistics.
[11] Edward S. Kim,et al. The BATTLE trial: personalizing therapy for lung cancer. , 2011, Cancer discovery.
[12] I. White. Estimating treatment effects in randomized trials with treatment switching , 2006, Statistics in medicine.
[13] Shein-Chung Chow,et al. Benefits, challenges and obstacles of adaptive clinical trial designs , 2011, Orphanet journal of rare diseases.
[14] Boris Freidlin,et al. Randomized clinical trials with biomarkers: design issues. , 2010, Journal of the National Cancer Institute.
[15] Frank Bretz,et al. Confirmatory Seamless Phase II/III Clinical Trials with Hypotheses Selection at Interim: General Concepts , 2006, Biometrical journal. Biometrische Zeitschrift.
[16] P F Thall,et al. A two-stage design for choosing among several experimental treatments and a control in clinical trials. , 1989, Biometrics.
[17] Shein-Chung Chow,et al. Adaptive design methods in clinical trials – a review , 2008, Orphanet journal of rare diseases.
[18] J O'Quigley,et al. Continual reassessment method: a practical design for phase 1 clinical trials in cancer. , 1990, Biometrics.
[19] D. DeMets,et al. Biomarkers and surrogate endpoints: Preferred definitions and conceptual framework , 2001, Clinical pharmacology and therapeutics.
[20] Janet Woodcock,et al. FDA introductory comments: clinical studies design and evaluation issues , 2005, Clinical trials.
[21] Bradley P. Carlin,et al. Bayesian Adaptive Methods for Clinical Trials , 2010 .
[22] M. Mugford,et al. Extracorporeal membrane oxygenation for severe respiratory failure in newborn infants. , 2008, The Cochrane database of systematic reviews.
[23] M. Christian,et al. Phase I clinical trial design in cancer drug development. , 2000, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[24] S. Chow,et al. Statistical Consideration of Adaptive Methods in Clinical Development , 2005, Journal of biopharmaceutical statistics.
[25] S. Chow,et al. Statistical inference for cancer trials with treatment switching , 2005, Statistics in medicine.
[26] M. Krams,et al. Adaptive Designs in Clinical Drug Development—An Executive Summary of the PhRMA Working Group , 2006, Journal of biopharmaceutical statistics.
[27] A. Gould. Planning and revising the sample size for a trial. , 1995, Statistics in Medicine.
[28] J. Cui,et al. Nonparametric Estimation of a Delay Distribution Based on Left‐Censored and Right‐Truncated Data , 1999, Biometrics.
[29] Aloka G Chakravarty,et al. Regulatory Aspects in Using Surrogate Markers in Clinical Trials , 2005, The Evaluation of Surrogate Endpoints.
[30] Allan R Sampson,et al. Drop‐the‐Losers Design: Normal Case , 2005, Biometrical journal. Biometrische Zeitschrift.
[31] Annpey Pong. Guest-Editor's Note: “Statistical Issues in Adaptive Design Methods in Clinical Trials” , 2007 .
[32] Tze Leung Lai,et al. Adaptive trial designs. , 2012, Annual review of pharmacology and toxicology.
[33] Michael A Proschan,et al. Two-Stage Sample Size Re-Estimation Based on a Nuisance Parameter: A Review , 2005, Journal of biopharmaceutical statistics.
[34] P. Bauer,et al. Evaluation of experiments with adaptive interim analyses. , 1994, Biometrics.
[35] A. Cohen,et al. Exact Tests That Recover Interblock Information in Balanced Incomplete Blocks Designs , 1989 .
[36] Mark Chang,et al. Adaptive Design Methods in Clinical Trials , 2006 .
[37] K. Gabriel,et al. On closed testing procedures with special reference to ordered analysis of variance , 1976 .
[38] Richard Simon,et al. Roadmap for developing and validating therapeutically relevant genomic classifiers. , 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[39] Alexia Iasonos,et al. A Comprehensive Comparison of the Continual Reassessment Method to the Standard 3 + 3 Dose Escalation Scheme in Phase I Dose-Finding Studies , 2008, Clinical trials.
[40] David B. Dunson,et al. Bayesian Data Analysis , 2010 .
[41] R. G. Cornell,et al. Extracorporeal circulation in neonatal respiratory failure: a prospective randomized study. , 1985, Pediatrics.
[42] S. Chow,et al. On the Independence of Data Monitoring Committee in Adaptive Design Clinical Trials , 2012, Journal of biopharmaceutical statistics.
[43] Boris Freidlin,et al. Biomarker-adaptive clinical trial designs. , 2010, Pharmacogenomics.
[44] J. Whitehead,et al. Estimating a treatment effect in survival studies in which patients switch treatment , 2002, Statistics in medicine.
[45] Daniel J Sargent,et al. Clinical trial designs for predictive marker validation in cancer treatment trials. , 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.