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Prediction of human pharmacokinetics of activated recombinant factor VII and B-domain truncated factor VIII from animal population pharmacokinetic models of haemophilia

Larsen, Malte Selch (författare)
Novo Nordisk AS, Global Res, Haemophilia Res, Haemophilia PK & ADME, Malov, Denmark.;Univ Copenhagen, Dept Vet Clin Sci, Frederiksberg, Denmark.
Juul, Rasmus Vestergaard (författare)
Novo Nordisk AS, Quantitat Clin Pharmacol, Soborg, Denmark.
Groth, Andreas Velsing (författare)
Novo Nordisk AS, Quantitat Clin Pharmacol, Soborg, Denmark.
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Simonsson, Ulrika S H, Professor (författare)
Uppsala universitet,Institutionen för farmaceutisk biovetenskap
Kristensen, Annemarie T. (författare)
Univ Copenhagen, Dept Vet Clin Sci, Frederiksberg, Denmark.
Knudsen, Tom (författare)
Novo Nordisk AS, Global Res, Haemophilia Pharmacol, Translat Haemophilia Pharmacol, Malov, Denmark.
Agersö, Henrik (författare)
Novo Nordisk AS, Quantitat Clin Pharmacol, Soborg, Denmark.
Kreilgaard, Mads (författare)
Novo Nordisk AS, Global Res, Haemophilia Res, Haemophilia PK & ADME, Malov, Denmark.
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Novo Nordisk AS, Global Res, Haemophilia Res, Haemophilia PK & ADME, Malov, Denmark;Univ Copenhagen, Dept Vet Clin Sci, Frederiksberg, Denmark. Novo Nordisk AS, Quantitat Clin Pharmacol, Soborg, Denmark. (creator_code:org_t)
ELSEVIER SCIENCE BV, 2018
2018
Engelska.
Ingår i: European Journal of Pharmaceutical Sciences. - : ELSEVIER SCIENCE BV. - 0928-0987 .- 1879-0720. ; 115, s. 196-203
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Various experimental animal models are used in haemophilia research, however, little is known about how well the different species predict pharmacokinetic (PK) profiles in haemophilia patients. The aim of the current study was to describe the plasma concentration-time profile of recombinant activated factor VII (rFVIIa) and recombinant factor VIII (rFVIII) in several experimental animal models using population PK modelling, and apply a simulation-based approach to evaluate how well the developed animal population PK models predict human PK. PK models were developed for rFVIIa and rFVIII in mice, rats, monkeys, and dogs using nonlinear mixed-effects modelling, accounting for inter-individual variability, nonlinear kinetics and covariate effects. Three scaling principles were applied to predict human PK: proportional scaling to body weight from single species, scaling with fixed theory-based allometric exponents from single species, and allometric interspecies scaling with estimated allometric coefficients and exponents. The plasma concentration-time profile of rFVIIa and rFVIII in mice, rats, monkeys and dogs were accurately described by the developed species-specific PK models, accounting for nonlinear kinetics and gender-specific difference in clearance for rFVIII. The predictive performance of the animal population PK models of rFVIIa and rFVIII revealed significant species-variation. The developed PK models of rFVIIa and rFVIII in monkeys and dogs along with allometric interspecies scaling revealed high predictive performance for human PK, and may promote rational decision-making in future first-in-human trials for rFVIIa and rFVIII variants.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

Nyckelord

Allometric scaling
Coagulation factors
Pharmacokinetic modelling
Interspecies
Prediction

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