modelM05BX05

Diagram of M05BX05

Extends from Pharmacokinetic.Models.PK_1C.

Information

name:Burosumab
ATC code:M05BX05
route:subcutaneous
compartments:1
dosage:1mg
volume of distribution:8.0L
clearance:0.29L/day
other parameters in model implementation

Burosumab is a fully human monoclonal antibody targeting fibroblast growth factor 23 (FGF23). It is used for the treatment of X-linked hypophosphatemia (XLH) in adults and children 1 year of age and older. It is an approved drug for this indication in the US and EU.

Pharmacokinetics

Pharmacokinetic parameters reported for adult and pediatric patients with X-linked hypophosphatemia following subcutaneous administration. Based on population PK analysis.

References

  1. Lee, SK, et al., & Shi, J (2022). Population Pharmacokinetics and Pharmacodynamics of Burosumab in Adult and Pediatric Patients With X-linked Hypophosphatemia. Journal of clinical pharmacology 62(1) 87–98. DOI:10.1002/jcph.1950 PUBMED:https://pubmed.ncbi.nlm.nih.gov/34352114

  2. Zhang, X, et al., & Carpenter, TO (2016). Population pharmacokinetic and pharmacodynamic analyses from a 4-month intradose escalation and its subsequent 12-month dose titration studies for a human monoclonal anti-FGF23 antibody (KRN23) in adults with X-linked hypophosphatemia. Journal of clinical pharmacology 56(4) 429–438. DOI:10.1002/jcph.611 PUBMED:https://pubmed.ncbi.nlm.nih.gov/26247790

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

Connectors

TypeNameDefaultDescription
Types.ConcentrationOutputC_central (from PK_1C)
Interfaces.ConcentrationPort_bcentralCPort (from PK_1C)

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

Revisions

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