ABSTRACT
In clinical research, power analysis is often performed for the sample size calculation. The purpose is to achieve a desired power of correctly detecting a clinically meaningful difference at a pre-specified level of significance if such a difference truly exists. However, in some situations such as (i) clinical trials with extremely low incidence rates and (ii) for rare disease drug development clinical trials, power analysis for sample size calculation may not be feasible because (i) it may require a huge sample size for detecting a relatively small difference and (ii) eligible patients may not be available for a small target patient population. In these cases, other procedures for sample size determination with certain statistical assurance are needed. In this chapter, an innovative method based on a probability monitoring procedure is proposed for sample size determination. The concept is to select an appropriate sample size for controlling the probability of crossing safety and/or efficacy boundaries. For rare disease clinical development, an adaptive probability monitoring procedure may be applied if a multiple-stage adaptive trial design is used.
