“…The MBMA utilizes pharmacological models such as the exposure–response relationship to characterize the effect of the drug, dose, study design, and patient covariates on the clinical outcome [ 32 ]. Most PE evaluations (e.g., Markov models) are empirical, obtaining their probabilities of drug efficacy and safety measures from a variety of sources (e.g., randomized trials, systematic reviews, observational studies, real-world data) and do not consider the mechanistic nature inherent of drug action (i.e., pharmacokinetics, pharmacodynamics, disease progression, and real-world scenarios such as adherence) [ 33 ]. Thus, the integration of pharmacometric and PE models provides an opportunity to predict future PE outcomes.…”