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Pharmaceutical Statistics|June 23, 2017
Equal-tailed confidence intervals for comparison of ratesPeter J LaudPharmaceutical Statistics|June 21, 2017
Missing data in clinical trials: control-based mean imputation and sensitivity analysisDevan V Mehrotra, Fang Liu, Thomas PermuttPharmaceutical Statistics|August 2, 2018
Bayesian dose-finding phase I trial design incorporating pharmacokinetic assessment in the field of oncologyKentaro Takeda, Kanji Komatsu, Satoshi MoritaPharmaceutical Statistics|April 21, 2018
Estimating the variance for heterogeneity in arm-based network meta-analysisHans-Peter Piepho, Laurence V Madden, James Roger, et al.Pharmaceutical Statistics|July 13, 2018
Covariate adjustment and estimation of mean response in randomised trialsJonathan W BartlettPharmaceutical Statistics|June 9, 2018
SPIRIT: A seamless phase I/II randomized design for immunotherapy trialsBeibei Guo, Daniel Li, Ying YuanPharmaceutical Statistics|June 30, 2018
Decision-making in drug development using a composite definition of successGaelle Saint-Hilary, Veronique Robert, Mauro GaspariniPharmaceutical Statistics|June 17, 2017
Testing for bioequivalence of highly variable drugs from TR-RT crossover designs with heterogeneous residual variancesQing Kang, Christopher I VahlPharmaceutical Statistics|July 11, 2017
Bayesian adaptive dose-escalation designs for simultaneously estimating the optimal and maximum safe dose based on safety and efficacyWai Yin Yeung, Bruno Reigner, Ulrich Beyer, et al.Pharmaceutical Statistics|September 2, 2016
On logistic regression analysis of dichotomized responsesKaifeng LuPageof 119