Abstract
Drug approval is based on exposure, response, and variability of studied populations, typically excluding comorbidities/medications and very ill patients, thus not representing real-world populations. This results in wide variability in therapeutic outcome for individual patients. Model-informed precision dosing
(MIPD) can characterize/quantify this variability, support optimal dose selection, and enable individualized therapy. The aim of this perspective is to raise awareness for MIPD, identify challenges hindering its implementation in clinical practice, provide recommendations, and highlight opportunities.
(MIPD) can characterize/quantify this variability, support optimal dose selection, and enable individualized therapy. The aim of this perspective is to raise awareness for MIPD, identify challenges hindering its implementation in clinical practice, provide recommendations, and highlight opportunities.
Original language | English |
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Pages (from-to) | 29-36 |
Number of pages | 8 |
Journal | Clinical Pharmacology and Therapeutics |
Volume | 109 |
Issue number | 1 |
Early online date | 17 Oct 2020 |
DOIs | |
Publication status | Published - Jan 2021 |