modelB02BD02

Diagram of B02BD02

Extends from Pharmacokinetic.Models.PK_2C.

Information

name:CoagulationFactorViii
ATC code:B02BD02
route:intravenous
compartments:2
dosage:50mg
volume of distribution:0.05L
clearance:3.5mL/h/kg
other parameters in model implementation

Coagulation factor VIII is a multifunctional glycoprotein playing a crucial role in the blood clotting cascade. It is primarily used for the treatment and prophylaxis of bleeding in individuals with hemophilia A, a genetic deficiency of factor VIII. Factor VIII is approved as a replacement therapy and is administered as either plasma-derived or recombinant concentrate products.

Pharmacokinetics

Pharmacokinetic parameters reported in adult patients with severe hemophilia A who received a single intravenous dose of recombinant factor VIII concentrate.

References

  1. Jiménez-Yuste, V, et al., & Møss, J (2015). The pharmacokinetics of a B-domain truncated recombinant factor VIII, turoctocog alfa (NovoEight®), in patients with hemophilia A. Journal of thrombosis and haemostasis : JTH 13(3) 370–379. DOI:10.1111/jth.12816 PUBMED:https://pubmed.ncbi.nlm.nih.gov/25495795

  2. Bolon-Larger, M, et al., & Boulieu, R (2007). A limited sampling strategy for estimating individual pharmacokinetic parameters of coagulation factor VIII in patients with hemophilia A. Therapeutic drug monitoring 29(1) 20–26. DOI:10.1097/FTD.0b013e3180311384 PUBMED:https://pubmed.ncbi.nlm.nih.gov/17304146

  3. Young, G, et al., & Allen, G (2015). Recombinant factor VIII Fc fusion protein for the prevention and treatment of bleeding in children with severe hemophilia A. Journal of thrombosis and haemostasis : JTH 13(6) 967–977. DOI:10.1111/jth.12911 PUBMED:https://pubmed.ncbi.nlm.nih.gov/25912075

Parameters

TypeNameDefaultDescription
Modelica.Units.SI.Massweight (from PK_1C)75patient weight (kg)
Modelica.Units.SI.SpecificVolumeVdPerKg (from PK_1C)0.9Volume of distribution (L/kg)
Modelica.Units.SI.MassFractionF (from PK_1C)0.8bioavailiability (0-1)
Pharmacolibrary.Types.ClearanceCl (from PK_1C)20clearance
Modelica.Units.SI.TimeadminTime (from PK_1C)60first administration time (s)
Modelica.Units.SI.TimeadminDuration (from PK_1C)600administration duration (s)
Modelica.Units.SI.TimeadminPeriod (from PK_1C)8*60*60period of administration (default 8 hours)(s)
Pharmacolibrary.Types.MassadminMass (from PK_1C)1000administration mass (mg)
IntegeradminCount (from PK_1C)8number of dose administered (1)
Pharmacolibrary.Types.VolumeVd (from PK_1C)VdPerKg*weightVolume of distribution (m3)
Pharmacolibrary.Types.MassConcentrationCmin (from PK_1C)0.004minimal therapeutic range
Pharmacolibrary.Types.MassConcentrationCmax (from PK_1C)0.008minimal therapeutic range
Pharmacolibrary.Types.MassConcentrationCtox_peak (from PK_1C)0.012toxicity peak level
Pharmacolibrary.Types.MassConcentrationCtox_trough (from PK_1C)0.006toxicity trough level
Pharmacolibrary.Types.VolumeVdp (from PK_2C)VdpPerKg*weightVolume of distribution (m3)
Modelica.Units.SI.SpecificVolumeVdpPerKg (from PK_2C)0.9Volume of distribution peripheral(l/kg)
Pharmacolibrary.Types.Clearancek12 (from PK_2C)1intercompartmental C-P clearance
Pharmacolibrary.Types.Clearancek21 (from PK_2C)1intercompartmental P-C clearance

Connectors

TypeNameDefaultDescription
Types.ConcentrationOutputC_central (from PK_1C)
Interfaces.ConcentrationPort_bcentralCPort (from PK_1C)
Interfaces.ConcentrationPort_bperipheralCPort (from PK_2C)
Pharmacolibrary.Types.ConcentrationOutputC_peripheral1 (from PK_2C)

Components

TypeNameDefaultDescription
Pharmacokinetic.NoPerfusedTissueCompartmentcentral (from PK_1C)
Pharmacokinetic.ClearanceDrivenEliminationelim (from PK_1C)
Sources.PeriodicDoseperiodicDose (from PK_1C)
Modelica.Units.SI.Timet1_2 (from PK_1C)elimination half-life
Pharmacolibrary.Pharmacokinetic.TransferFirstOrderNonSymtransfer (from PK_2C)
Pharmacolibrary.Pharmacokinetic.NoPerfusedTissueCompartmentperipheral (from PK_2C)

Revisions

  • 06/2025 Tomas Kulhanek, generated model from data extracted from PUBMED, DrugBank and LLM(GPT4.1)