Uses the clinician elicited prior reference probabilities for each subgroup and dose to obtain prior means for the Bayesian logistic regression model used in the SubTite trial design.
#Groups X #Doses matrix containing the elicited prior toxicity probabilities at the reference time for each dose and subgroup.
Vector containing standardized doses.
Returns the a list containing the nonlinear regression model whos parameter estimates will be used as prior means for the SubTITE Design.
 Chapple and Thall (2017), Subgroup-specific dose finding in phase I clinical trials based on time to toxicity allowing adaptive subgroup combination
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