Why the racing industry and equestrian disciplines need to implement population pharmacokinetics: To learn, explain, summarize, harmonize, and individualize

Author:

Toutain Pierre‐Louis12ORCID

Affiliation:

1. INTHERES Université de Toulouse, INRAE, ENVT Toulouse France

2. The Royal Veterinary College University of London London UK

Abstract

AbstractPopulation pharmacokinetics (POP PK) is a powerful pharmacokinetic tool, which measures quantitatively, and explains the variability in drug exposure and drug effect between individuals. POP PK uses an observational (nonexperimental) approach; it is conducted in the target population living in its normal environment (e.g., farm and race‐track). The strength of the POP PK approach lies in its greater relevance for the population studied in its different natural environments than experimental studies carried out in more or less biased laboratory conditions. In clinical settings, it is commonly necessary to restrict the number of samples per subject collected for analysis and the derived data cannot be analyzed using traditional individual data analytical methods; rather data are merged and analyzed with an appropriate statistical tool: the nonlinear mixed effect model (NLMEM). POP PK modeling is frequently used with the objective of adjusting drug dosage, and hence drug exposure, not only for the whole population but also for subgroups of animals (e.g., for a given breed, sex, and age). It can also have application at the individual subject level, in the context of precision medicine. For horses, the use of the POP PK/PD model will allow prescribers to estimate an individual Withdrawal Time for a given horse whose treatment they are supervising. Another potential field of application will be meta‐analysis of existing data to generate new knowledge on a drug or to collate and synthesize, in an objective and transparent manner, existing data; this will facilitate harmonization of screening limits at an international level.

Publisher

Wiley

Reference34 articles.

1. U.S. Department of Health and Human Services Food and Drug Administration.Guidance for Industry. Population Pharmacokinetics. Department of Health and Human Services Food and Drug Administration. Accessed March 09 2023.https://www.fda.gov/regulatory-information/search-fda-guidance-documents/population-pharmacokinetics

2. European Medicine agency.Guideline on reporting the results of population pharmacokinetic analyses. CHMP/EWP/185990/06. Accessed March 09 2023.https://www.ema.europa.eu/en/documents/scientific-guideline/guideline-reporting-results-population-pharmacokinetic-analyses_en.pdf

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