Physiologically‐based pharmacokinetics of ziprasidone in pregnant women

Aim

Pregnancy is associated with physiological changes that alter the pharmacokinetics (PK) of drugs. The aim was to predict the PK of ziprasidone in pregnant women.

Methods

A full PBPK model of ziprasidone was developed and validated for the non‐pregnant population (healthy adults, pediatrics, geriatrics) and this was extended to the pregnant state to assess the change in PK profile of ziprasidone throughout pregnancy.

Results

PBPK model successfully predicted the ziprasidone disposition in healthy adult volunteers, wherein the predicted and observed AUC, C_max, and t_max were within the fold‐difference of 0.94‐1.09, 0.89‐1.40, and 0.80‐1.08, respectively. Pediatric and geriatric population, also showed predicted AUC, C_max and t_max within a two‐fold range of the observed values. The simulated exposure in pregnant women using p‐PBPK model showed no significant difference when compared to non‐pregnant women.

Conclusions

The PBPK model predicted the impact of physiological changes during pregnancy on PK and exposure of ziprasidone, suggesting that dose adjustment is not necessary in this special population.

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