On the choice of doses for phase III clinical trials
Journal article, 2013

Many potential new medicines fail in phase III clinical trials, because of either insufficient efficacy or intolerability. Such failures may be caused by the absence of an effect and also if a suboptimal dose is being tested. It is thus important to consider how to optimise the choice of dose or doses that continue into the confirmatory phase. For many indications, it is common to test one single active dose in phase III. However, phase IIB dose-finding trials are relatively small and often lack the ability of precisely estimating the dose–response curves for efficacy and tolerability. Because of this uncertainty in dose response, it is reasonable to consider bringing more than one dose into phase III. Using simple but illustrative models, we find the optimal doses and compare the probability of success, for fixed total sample sizes, when one or two active doses are included in phase III.

benefit/risk

optimal doses

Bayesian decision analysis

design of clinical trials

probability of success

multiple testing

Author

Vera Lisovskaja

University of Gothenburg

Chalmers, Mathematical Sciences, Mathematical Statistics

Carl-Fredrik Burman

University of Gothenburg

Chalmers, Mathematical Sciences, Mathematical Statistics

Statistics in Medicine

0277-6715 (ISSN) 1097-0258 (eISSN)

Vol. 32 10 1661-1676

Subject Categories

Probability Theory and Statistics

DOI

10.1002/sim.5632

More information

Created

10/7/2017