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Journal of Biopharmaceutical Statistics Volume 22, 2012 - Issue 4: Adaptive Designs for Clinical Trials: Considerations about and Beyond the FDA Adaptive Designs Guidance
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Original Articles

Sample Size Adaptation in Fixed-Dose Combination Drug Trial

H. M. James Hung Division of Biometrics I, OB/OTS/CDER, U.S. Food and Drug Administration, Silver Spring, Maryland, USACorrespondence[email protected]
&
Sue-Jane Wang Office of Biostatictics, OTS/CDER, U.S. Food and Drug Administration, Silver Spring, Maryland, USA
Pages 679-686 | Received 19 Feb 2011, Accepted 28 Jan 2012, Published online: 31 May 2012

Citations (3)

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Read on this site (1)

H. M. James Hung, Sue-Jane Wang & Peiling Yang. (2014) Some Challenges With Statistical Inference in Adaptive Designs. Journal of Biopharmaceutical Statistics 24:5, pages 1059-1072.
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Articles from other publishers (2)

Lawrence M. Friedman, Curt D. Furberg, David L. DeMets, David M. Reboussin & Christopher B. GrangerLawrence M. Friedman, Curt D. Furberg, David L. DeMets, David M. Reboussin & Christopher B. Granger. 2015. Fundamentals of Clinical Trials. Fundamentals of Clinical Trials 373 401 .
H Hung & Sue-Jane Wang. 2014. Clinical Trial Biostatistics and Biopharmaceutical Applications. Clinical Trial Biostatistics and Biopharmaceutical Applications 3 40 .

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