Design and Analysis of Cross-Over Trials
This third edition contains new chapters on re-estimating sample size when testing for average bioequivalence, fitting a nonlinear dose response function, estimating a dose to take forward from phase two to phase three, establishing proof of concept, and recalculating the sample size using conditional power. It employs the specially creat
Oktober 2024, ca. 438 Seiten, Chapman & Hall/CRC Monographs on Statistics and Applied Probability, Englisch
Taylor and Francis
978-1-032-91989-8