modelBlinatumomab

Diagram of Blinatumomab

Extends from Pharmacolibrary.Drugs.ATC.L.L01FX07.

Information

name:Blinatumomab
ATC code:L01FX07
route:intravenous
compartments:2
dosage:28mg
volume of distribution:4.35L
clearance:2.92L/h
other parameters in model implementation

Blinatumomab is a bispecific T-cell engager (BiTE) monoclonal antibody used in the treatment of acute lymphoblastic leukemia (ALL). It binds CD19 on B-cells and CD3 on T-cells, directing cytotoxic T-cells to kill malignant B-cells. Blinatumomab is approved for the treatment of relapsed or refractory B-cell precursor ALL in adults and children.

Pharmacokinetics

Pharmacokinetic parameters reported in adults (18–77 years) with relapsed or refractory B-cell precursor acute lymphoblastic leukemia treated with intravenous blinatumomab. Parameters obtained at steady-state during continuous intravenous infusion.

References

  1. Clements, JD, et al., & Doshi, S (2020). Population Pharmacokinetics of Blinatumomab in Pediatric and Adult Patients with Hematological Malignancies. Clinical pharmacokinetics 59(4) 463–474. DOI:10.1007/s40262-019-00823-8 PUBMED:https://pubmed.ncbi.nlm.nih.gov/31679130

  2. Zhu, M, et al., & Doshi, S (2016). Blinatumomab, a Bispecific T-cell Engager (BiTE(®)) for CD-19 Targeted Cancer Immunotherapy: Clinical Pharmacology and Its Implications. Clinical pharmacokinetics 55(10) 1271–1288. DOI:10.1007/s40262-016-0405-4 PUBMED:https://pubmed.ncbi.nlm.nih.gov/27209293

  3. Kaplan, JB, et al., & Giles, FJ (2015). Blinatumomab for the treatment of acute lymphoblastic leukemia. Investigational new drugs 33(6) 1271–1279. DOI:10.1007/s10637-015-0289-4 PUBMED:https://pubmed.ncbi.nlm.nih.gov/26383529

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)