Zobrazeno 1 - 10
of 67
pro vyhledávání: '"H. M James Hung"'
Autor:
H. M. James Hung, John Lawrence
Publikováno v:
Statistics in Biopharmaceutical Research. 15:318-322
Over the last several decades, major adverse clinical outcomes have been studied in the form of composite endpoints in cardiovascular and renal trials. Great utilities and challenges in the use of ...
Publikováno v:
Therapeutic Innovation & Regulatory Science. 55:197-211
Uncertain ascertainment of events in clinical trials has been noted for decades. To correct possible bias, Clinical Endpoint Committees (CECs) have been employed as a critical element of trials to ensure consistent and high-quality endpoint evaluatio
Autor:
H. M. James Hung, Sue-Jane Wang
Publikováno v:
Statistics in Biopharmaceutical Research. 15:249-250
Publikováno v:
Statistics in Biopharmaceutical Research. 11:239-251
Polycystic kidney disease is a genetic disorder that causes cysts to grow in the kidney. It is slowly progressing and often leads to end-stage kidney disease, requiring dialysis or a transp...
Autor:
Norman Stockbridge, Bruce Binkowitz, Mouna Akacha, H. M. James Hung, Guenther Mueller-Velten, Brian Claggett
Publikováno v:
Therapeutic Innovation & Regulatory Science. 53:387-397
Serious and chronic health conditions such as cardiovascular diseases (CVDs) are posing challenges to the health system. Recently clinical trials in these fields have focused on composite endpoints that take into account both disease-related mortalit
Publikováno v:
Journal of Biopharmaceutical Statistics. 29:1116-1129
The sequential parallel comparison designhas recently been considered to solve the problem with high placebo response and the required sample size in the psychiatric clinical trials. One feature with this design is that a difference between the place
Publikováno v:
Contemp Clin Trials
We investigate selection of critical boundary functions for testing the hypotheses of two time-to-event outcomes as both primary endpoints or a primary and a secondary endpoint in group-sequential clinical trials, where (1) the effect sizes of endpoi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77fceefc98db6be1689caccdf32eaf95
https://europepmc.org/articles/PMC7954908/
https://europepmc.org/articles/PMC7954908/
Publikováno v:
Journal of Biopharmaceutical Statistics. 29:1134-1136
In this rejoinder the authors stipulate further for two challenging issues. First, if placebo non-responders are selected simply by their response meeting a threshold, this selection may have miscl...
Autor:
Eugenio Andraca-Carrera, Thomas Gwise, Stella Grosser, Somesh Chattopadhyay, Sue Jane Wang, Anup K. Amatya, Mark Rothmann, Fraser Smith, Sylva H. Collins, Rebecca Rothwell, Yu-Ting Weng, Yute Wu, H. M. James Hung
Publikováno v:
Statistics in Biopharmaceutical Research. 13:57-58
Null hypothesis testing is a foundational stone of statistical analysis. The “p-value” has evolved to play a critical role in hypothesis testing. Nonetheless, use of p-values carries with it some c...
Publikováno v:
Statistics in Biopharmaceutical Research. 13:30-31
We are grateful for the opportunity to enjoy reading the article by Dr. Eric Gibson (Gibson 2020). The article covers a lot of important subjects concerning strength of evidence very well. The sugg...