modelR03DX05

Extends from Pharmacokinetic.Models.PK_2C.

Information

name:Omalizumab
ATC code:R03DX05
route:subcutaneous
compartments:2
dosage:150mg
volume of distribution:7.47L
clearance:2.4mL/min
other parameters in model implementation

Omalizumab is a humanized monoclonal antibody that selectively binds to immunoglobulin E (IgE). It is primarily used as an add-on therapy for moderate to severe persistent allergic asthma not adequately controlled with inhaled corticosteroids. Omalizumab is also approved for treatment of chronic spontaneous urticaria. The drug is administered subcutaneously and is approved in the United States, Europe, and many other countries.

Pharmacokinetics

Population pharmacokinetics in adult and adolescent patients with moderate to severe allergic asthma after subcutaneous administration.

References

  1. Luu, M, et al., & Goirand, F (2016). Pharmacokinetics, pharmacodynamics and clinical efficacy of omalizumab for the treatment of asthma. Expert opinion on drug metabolism & toxicology 12(12) 1503–1511. DOI:10.1080/17425255.2016.1248403 PUBMED:https://pubmed.ncbi.nlm.nih.gov/27748630

  2. Plosker, GL, & Keam, SJ (2008). Omalizumab: a review of its use in the treatment of allergic asthma. BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy 22(3) 189–204. DOI:10.2165/00063030-200822030-00005 PUBMED:https://pubmed.ncbi.nlm.nih.gov/18481901

  3. Lowe, PJ, et al., & Jimenez, P (2009). Relationship between omalizumab pharmacokinetics, IgE pharmacodynamics and symptoms in patients with severe persistent allergic (IgE-mediated) asthma. British journal of clinical pharmacology 68(1) 61–76. DOI:10.1111/j.1365-2125.2009.03401.x PUBMED:https://pubmed.ncbi.nlm.nih.gov/19660004

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)