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Statistics in Medicine
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March 23, 2012
Testing superiority at interim analyses in a non-inferiority trial
Y H Joshua Chen, Cong Chen
Journal of Biopharmaceutical Statistics
|
July 9, 2008
On methods to utilize HIV-RNA data measured by two different PCR assays
Y H Joshua Chen, Chunpeng Fan, Jing Zhao
Journal of Biopharmaceutical Statistics
|
May 27, 2006
Testing for crossover of two hazard functions using Gail and Simon's method
Y H Joshua Chen, G H Frank Liu
Clinical Trials (London, England)
|
October 4, 2014
A seamless phase IIB/III adaptive outcome trial: design rationale and implementation challenges
Y H Joshua Chen, Richard Gesser, Alain Luxembourg
Journal of Biopharmaceutical Statistics
|
October 8, 2004
Incorporating durability information in the comparison of proportions of patients with HIV suppression
Y H Joshua Chen, Michael L Nessly, Balasamy Thiyagarajan
Journal of Biopharmaceutical Statistics
|
August 30, 2017
Statistical inference following sample size adjustment based on the 50%-conditional-power principle
Y H Joshua Chen, Shuai S Yuan, Xiaoming Li
Clinical Trials (London, England)
|
July 22, 2015
Sample size adjustment based on promising interim results and its application in confirmatory clinical trials
Y H Joshua Chen, Caiyan Li, K K Gordon Lan
Statistics in Medicine
|
November 24, 2004
Treatment comparisons for a partially categorical outcome applied to a biomarker with assay limit
Y H Joshua Chen, A Lawrence Gould, Michael L Nessly
Statistics in Medicine
|
July 27, 2010
Some drop-the-loser designs for monitoring multiple doses
Y H Joshua Chen, David L Demets, K K Gordon Lan
Controlled Clinical Trials
|
February 1, 2003
Monitoring mortality at interim analyses while testing a composite endpoint at the final analysis
Y H Joshua Chen, David L DeMets, K K Gordon Lan
Page
of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Statistics in Medicine
|
March 23, 2012
Testing superiority at interim analyses in a non-inferiority trial
Y H Joshua Chen, Cong Chen
Journal of Biopharmaceutical Statistics
|
July 9, 2008
On methods to utilize HIV-RNA data measured by two different PCR assays
Y H Joshua Chen, Chunpeng Fan, Jing Zhao
Journal of Biopharmaceutical Statistics
|
May 27, 2006
Testing for crossover of two hazard functions using Gail and Simon's method
Y H Joshua Chen, G H Frank Liu
Clinical Trials (London, England)
|
October 4, 2014
A seamless phase IIB/III adaptive outcome trial: design rationale and implementation challenges
Y H Joshua Chen, Richard Gesser, Alain Luxembourg
Journal of Biopharmaceutical Statistics
|
October 8, 2004
Incorporating durability information in the comparison of proportions of patients with HIV suppression
Y H Joshua Chen, Michael L Nessly, Balasamy Thiyagarajan
Journal of Biopharmaceutical Statistics
|
August 30, 2017
Statistical inference following sample size adjustment based on the 50%-conditional-power principle
Y H Joshua Chen, Shuai S Yuan, Xiaoming Li
Clinical Trials (London, England)
|
July 22, 2015
Sample size adjustment based on promising interim results and its application in confirmatory clinical trials
Y H Joshua Chen, Caiyan Li, K K Gordon Lan
Statistics in Medicine
|
November 24, 2004
Treatment comparisons for a partially categorical outcome applied to a biomarker with assay limit
Y H Joshua Chen, A Lawrence Gould, Michael L Nessly
Statistics in Medicine
|
July 27, 2010
Some drop-the-loser designs for monitoring multiple doses
Y H Joshua Chen, David L Demets, K K Gordon Lan
Controlled Clinical Trials
|
February 1, 2003
Monitoring mortality at interim analyses while testing a composite endpoint at the final analysis
Y H Joshua Chen, David L DeMets, K K Gordon Lan
Page
of 2