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Pharmaceutical Statistics|March 14, 2007
Handling drop-out in longitudinal clinical trials: a comparison of the LOCF and MMRM approachesPeter LanePharmaceutical Statistics|July 27, 2007
Partition testing in dose-response studies with multiple endpointsYi Liu, Jason Hsu, Stephen RubergPharmaceutical Statistics|November 30, 2006
Assessment of the Gould-Shih procedure for sample size re-estimationJoel A WaksmanPharmaceutical Statistics|May 30, 2007
Sodium cromoglicate: an ineffective drug or meta-analysis misused?M T Stevens, A M Edwards, J B L HowellPharmaceutical Statistics|June 1, 2007
Global benefit-risk assessment in designing clinical trials and some statistical considerations of the methodYili Lu Pritchett, Roy TamuraPharmaceutical Statistics|January 26, 2007
A two-stage phase II trial design utilizing both primary and secondary endpointsXun Lin, Randy Allred, Glen AndrewsPharmaceutical Statistics|December 1, 2006
Combining estimates from multiple early studies to obtain estimates of response: using shrinkage estimates to obtain estimates of responseSteven J Kathman, Michael D HalePharmaceutical Statistics|November 28, 2006
Sample size and the probability of a successful trialChristy Chuang-SteinPharmaceutical Statistics|May 7, 2021
Conditional assurance: the answer to the questions that should be asked within drug developmentJane R Temple, Jon R RobertsonPharmaceutical Statistics|April 28, 2021
The use of external controls: To what extent can it currently be recommended?Hans Ulrich Burger, Christoph Gerlinger, Chris Harbron, et al.Pageof 120