The utility of microdosing over the past 5 years

A review of 18 drugs found that 15 showed linear pharmacokinetics, meaning their drug concentration profiles at a microdose (≤100 micrograms) fell within a factor of two of those at a therapeutic dose. This supports the use of microdosing in Phase 0 trials to predict how a drug will behave at clinically relevant doses, helping to select candidates for further testing.

Study at a glance

Abstract

BACKGROUND: Microdosing studies (human Phase 0) are used to select drug candidates for Phase I clinical trials on the basis of their pharmacokinetic properties, using subpharmacologic doses (maximum 100 microg). There are questions as to whether pharmacokinetic data obtained at these low doses will predict those at the clinically relevant dose. OBJECTIVE: To review the current literature on microdosing and assess how well microdose data have predicted the pharmacokinetics obtained at a therapeutic dose. METHODS: All data published in the peer reviewed literature comparing pharmacokinetics at a microdose with a therapeutic dose were reviewed, excluding those studies aimed at imaging. CONCLUSIONS: Of the 18 drugs reported, 15 demonstrated linear pharmacokinetics within a factor of 2 between a microdose and a therapeutic dose. Therefore, data that support the utility of microdosing are beginning to emerge.