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Pharmaceutical Statistics
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December 20, 2018
On weighted composite scores for early Alzheimer's trials
Kun Jin, Briana Cameron, Billy Dunn
Pharmaceutical Statistics
|
November 22, 2019
Two-stage phase II survival trial design
Jianrong Wu, Li Chen, Jing Wei, et al.
Pharmaceutical Statistics
|
October 31, 2019
Nonlinear mixed-effects models with misspecified random-effects distribution
Reza Drikvandi
Pharmaceutical Statistics
|
January 18, 2019
Nested combination tests with a time-to-event endpoint using a short-term endpoint for design adaptations
Silke Jörgens, Gernot Wassmer, Franz König, et al.
Pharmaceutical Statistics
|
January 18, 2019
Blinded sample size reestimation in event-driven clinical trials: Methods and an application in multiple sclerosis
Tim Friede, Harald Pohlmann, Heinz Schmidli
Pharmaceutical Statistics
|
January 31, 2019
Statistical considerations in a delayed-start design to demonstrate disease modification effect in neurodegenerative disorders
Deli Wang, Weining Robieson, Jun Zhao, et al.
Pharmaceutical Statistics
|
December 31, 2019
A flexible multi-domain test with adaptive weights and its application to clinical trials
Yang Zhao, Qifeng Yu, Stephen L Lake
Pharmaceutical Statistics
|
December 13, 2019
Testing treatment-by-period interaction in four-period crossover trials
Bo Li, Zaiying Zhou, Li Zhang, et al.
Pharmaceutical Statistics
|
December 13, 2019
TITE-BOIN-ET: Time-to-event Bayesian optimal interval design to accelerate dose-finding based on both efficacy and toxicity outcomes
Kentaro Takeda, Satoshi Morita, Masataka Taguri
Pharmaceutical Statistics
|
February 24, 2018
Bayesian approach for assessing noninferiority in a three-arm trial with binary endpoint
Santu Ghosh, Ram C Tiwari, Samiran Ghosh
Page
of 124
Search research articles
Search
Showing results (71-80 of 1,235) with videos related to
Sort By:
Page
of 124
Pharmaceutical Statistics
|
December 20, 2018
On weighted composite scores for early Alzheimer's trials
Kun Jin, Briana Cameron, Billy Dunn
Pharmaceutical Statistics
|
November 22, 2019
Two-stage phase II survival trial design
Jianrong Wu, Li Chen, Jing Wei, et al.
Pharmaceutical Statistics
|
October 31, 2019
Nonlinear mixed-effects models with misspecified random-effects distribution
Reza Drikvandi
Pharmaceutical Statistics
|
January 18, 2019
Nested combination tests with a time-to-event endpoint using a short-term endpoint for design adaptations
Silke Jörgens, Gernot Wassmer, Franz König, et al.
Pharmaceutical Statistics
|
January 18, 2019
Blinded sample size reestimation in event-driven clinical trials: Methods and an application in multiple sclerosis
Tim Friede, Harald Pohlmann, Heinz Schmidli
Pharmaceutical Statistics
|
January 31, 2019
Statistical considerations in a delayed-start design to demonstrate disease modification effect in neurodegenerative disorders
Deli Wang, Weining Robieson, Jun Zhao, et al.
Pharmaceutical Statistics
|
December 31, 2019
A flexible multi-domain test with adaptive weights and its application to clinical trials
Yang Zhao, Qifeng Yu, Stephen L Lake
Pharmaceutical Statistics
|
December 13, 2019
Testing treatment-by-period interaction in four-period crossover trials
Bo Li, Zaiying Zhou, Li Zhang, et al.
Pharmaceutical Statistics
|
December 13, 2019
TITE-BOIN-ET: Time-to-event Bayesian optimal interval design to accelerate dose-finding based on both efficacy and toxicity outcomes
Kentaro Takeda, Satoshi Morita, Masataka Taguri
Pharmaceutical Statistics
|
February 24, 2018
Bayesian approach for assessing noninferiority in a three-arm trial with binary endpoint
Santu Ghosh, Ram C Tiwari, Samiran Ghosh
Page
of 124