The continual reassessment method provides a new approach for estimati
ng the maximum tolerated dose in a phase I clinical trial. In this pap
er we investigate a potential stopping rule for this method. We indica
te certain situations in which the finally chosen dose level can be pr
edicted with certainty after having included a number of patients stri
ctly less than the projected sample size. There is therefore a clear g
ain when the only purpose of the trial is to identify a target dose fo
r future experimentation. When prediction with certainty is not possib
le, we can still estimate the probability that the current level will
be the same as all subsequent recommended levels.