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Journal of Biopharmaceutical Statistics|September 15, 2015
General guidance on exploratory and confirmatory subgroup analysis in late-stage clinical trialsAlex Dmitrienko, Christoph Muysers, Arno Fritsch, et al.Journal of Biopharmaceutical Statistics|September 15, 2015
Can sequential parallel comparison design and two-way enriched design be useful in medical device clinical trials?Anastasia Ivanova, Zhiwei Zhang, Laura Thompson, et al.Journal of Biopharmaceutical Statistics|August 8, 2014
Scientific factors and current issues in biosimilar studiesShein-Chung Chow, Laszlo Endrenyi, Peter A Lachenbruch, et al.Journal of Biopharmaceutical Statistics|July 18, 2014
Sample size determination for equivalence assessment with multiple endpointsAnna Sun, Xiaoyu Dong, Yi TsongJournal of Biopharmaceutical Statistics|July 18, 2014
Equivalence tests for interchangeability based on two one-sided probabilitiesXiaoyu Dong, Yi Tsong, Meiyu ShenJournal of Biopharmaceutical Statistics|July 19, 2014
Biosimilars: where we were and where we areRodeina Challand, Hazel Gorham, John ConstantJournal of Biopharmaceutical Statistics|July 19, 2014
On the lower predictive bound approach for noninferiority clinical trials with binary dataQing Liu, Yulan LiJournal of Biopharmaceutical Statistics|July 30, 2014
Frequency estimator for assessing of follow-on biologicsYing Lu, Zhong-Zhan Zhang, Shein-Chung ChowJournal of Biopharmaceutical Statistics|March 25, 2016
Extending the classification approach for comparing two active treatment arms to binary and time-to-event outcomesJingyi Liu, Yongming Qu, Pandurang M KulkarniJournal of Biopharmaceutical Statistics|March 25, 2016
Testing equality of proportions for correlated binary data in ophthalmologic studiesChang-Xing Ma, Song LiuPageof 216