Sample size for a noninferiority clinical trial with time-to-event data in the presence of competing risks (English)
- New search for: Han, Dong
- New search for: Chen, Zheng
- New search for: Hou, Yawen
- New search for: Han, Dong
- New search for: Chen, Zheng
- New search for: Hou, Yawen
In:
Journal of biopharmaceutical statistics
;
28
, 4
;
797-807
;
2018
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ISSN:
- Article (Journal) / Print
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Title:Sample size for a noninferiority clinical trial with time-to-event data in the presence of competing risks
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Contributors:
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Published in:Journal of biopharmaceutical statistics ; 28, 4 ; 797-807
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Publisher:
- New search for: Taylor & Francis
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Publication date:2018-01-01
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Size:11 pages
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ISSN:
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Type of media:Article (Journal)
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Type of material:Print
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Language:English
- New search for: 615.19
- Further information on Dewey Decimal Classification
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Classification:
DDC: 615.19 -
Source:
© Metadata Copyright the British Library Board and other contributors. All rights reserved.
Table of contents – Volume 28, Issue 4
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 589
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Sample size determination for the current strategy in oncology Phase 3 trials that tests progression-free survival and overall survival in a two-stage design frameworkNomura, Shogo / Hirakawa, Akihiro / Hamada, Chikuma et al. | 2018
- 612
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Time-dependent ROC analysis for censored biomarker data due to limit of detectionKim, Yeonhee / Kong, Lan et al. | 2018
- 622
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Timing of the interim analysis in adaptive enrichment designsBenner, Laura / Kieser, Meinhard et al. | 2018
- 633
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Differential losses to follow-up that are outcome-dependent can vitiate a clinical trial: Simulation resultsPotthoff, Richard F. et al. | 2018
- 645
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A comparison of multiple imputation methods for incomplete longitudinal binary dataYamaguchi, Yusuke / Misumi, Toshihiro / Maruo, Kazushi et al. | 2018
- 668
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Assessing performance of sequential analysis methods for active drug safety surveillance using observational dataZhou, Xiaofeng / Bao, Warren / Gaffney, Mike / Shen, Rongjun / Young, Sarah / Bate, Andrew et al. | 2018
- 682
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Confidence intervals for the common intraclass correlation in the analysis of clustered binary responsesSaha, Krishna K. / Wang, Suojin et al. | 2018
- 698
-
A decision theoretical modeling for Phase III investments and drug licensingMiller, Frank / Burman, Carl-Fredrik et al. | 2018
- 722
-
Influence Analysis for the Area Under the Receiver Operating Characteristic CurveKe, Bo-Shiang / Chiang, An Jen / Chang, Yuan-chin Ivan et al. | 2018
- 735
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Model selection based on combined penalties for biomarker identificationVradi, Eleni / Brannath, Werner / Jaki, Thomas / Vonk, Richardus et al. | 2018
- 750
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Subgroup analysis based on prognostic and predictive gene signatures for adjuvant chemotherapy in early-stage non-small-cell lung cancer patientsMoon, Hojin / Zhao, Yuan / Pluta, Dustin / Ahn, Hongshik et al. | 2018
- 763
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Parametric modeling and optimal experimental designs for estimating isobolograms for drug interactions in toxicologyHolland-Letz, Tim / Gunkel, Nikolas / Amtmann, Eberhard / Kopp-Schneider, Annette et al. | 2018
- 778
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The stratified win ratioDong, Gaohong / Qiu, Junshan / Wang, Duolao / Vandemeulebroecke, Marc et al. | 2018
- 797
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Sample size for a noninferiority clinical trial with time-to-event data in the presence of competing risksHan, Dong / Chen, Zheng / Hou, Yawen et al. | 2018