Literature DB >> 19040326

The utility of microdosing over the past 5 years.

Graham Lappin1, R Colin Garner.   

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.

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Year:  2008        PMID: 19040326     DOI: 10.1517/17425250802531767

Source DB:  PubMed          Journal:  Expert Opin Drug Metab Toxicol        ISSN: 1742-5255            Impact factor:   4.481


  19 in total

1.  Hormesis pervasiveness and its potential implications for pharmaceutical research and development.

Authors:  Kenneth I Maynard
Journal:  Dose Response       Date:  2011-07-29       Impact factor: 2.658

2.  Delivered dose: a drug-centric phenotype for chemotherapy dose individualization.

Authors:  Y Bruce Yu
Journal:  Pharm Res       Date:  2009-06-03       Impact factor: 4.200

Review 3.  Quantifying exploratory low dose compounds in humans with AMS.

Authors:  Stephen R Dueker; Le T Vuong; Peter N Lohstroh; Jason A Giacomo; John S Vogel
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4.  Simultaneous oral therapeutic and intravenous ¹⁴C-microdoses to determine the absolute oral bioavailability of saxagliptin and dapagliflozin.

Authors:  David W Boulton; Sreeneeranj Kasichayanula; Chi Fung Anther Keung; Mark E Arnold; Lisa J Christopher; Xiaohui Sophia Xu; Frank Lacreta
Journal:  Br J Clin Pharmacol       Date:  2013-03       Impact factor: 4.335

Review 5.  Modeling of PET data in CNS drug discovery and development.

Authors:  Katarina Varnäs; Andrea Varrone; Lars Farde
Journal:  J Pharmacokinet Pharmacodyn       Date:  2013-05-10       Impact factor: 2.745

6.  Use of microdose phenotyping to individualise dosing of patients.

Authors:  Nicolas Hohmann; Walter E Haefeli; Gerd Mikus
Journal:  Clin Pharmacokinet       Date:  2015-09       Impact factor: 6.447

Review 7.  Predictive Value of Microdose Pharmacokinetics.

Authors:  Merel van Nuland; Hilde Rosing; Alwin D R Huitema; Jos H Beijnen
Journal:  Clin Pharmacokinet       Date:  2019-10       Impact factor: 6.447

8.  Clinical Micro-Dose Studies to Explore the Human Pharmacokinetics of Four Selective Inhibitors of Human Nav1.7 Voltage-Dependent Sodium Channels.

Authors:  Hannah M Jones; Richard P Butt; Rob W Webster; Ian Gurrell; Pawel Dzygiel; Neil Flanagan; Daniela Fraier; Tanya Hay; Laura Else Iavarone; Jacquelynn Luckwell; Hannah Pearce; Alex Phipps; Jill Segelbacher; Bill Speed; Kevin Beaumont
Journal:  Clin Pharmacokinet       Date:  2016-07       Impact factor: 6.447

9.  A novel double-tracer technique to characterize absorption, distribution, metabolism and excretion (ADME) of [14C]tofogliflozin after oral administration and concomitant intravenous microdose administration of [13C]tofogliflozin in humans.

Authors:  Dietmar Schwab; Agnes Portron; Zoe Backholer; Berthold Lausecker; Kosuke Kawashima
Journal:  Clin Pharmacokinet       Date:  2013-06       Impact factor: 6.447

Review 10.  Microdosing and drug development: past, present and future.

Authors:  Graham Lappin; Robert Noveck; Tal Burt
Journal:  Expert Opin Drug Metab Toxicol       Date:  2013-04-04       Impact factor: 4.481

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