modelObinutuzumab

Diagram of Obinutuzumab

Extends from Pharmacolibrary.Drugs.ATC.L.L01FA03.

Information

name:Obinutuzumab
ATC code:L01FA03
route:intravenous
compartments:2
dosage:1000mg
volume of distribution:3.8L
clearance:0.09L/h
other parameters in model implementation

Obinutuzumab is a glycoengineered humanized type II anti-CD20 monoclonal antibody used primarily in the treatment of chronic lymphocytic leukemia (CLL) and follicular lymphoma. It acts by targeting the CD20 antigen on B lymphocytes, resulting in cell lysis. Obinutuzumab is approved for clinical use in various countries.

Pharmacokinetics

Pharmacokinetic parameters reported for adult patients with relapsed or refractory CD20-positive B-cell malignancies following intravenous administration.

References

  1. Zhai, J, et al., & Shi, J (2017). Pharmacokinetics of obinutuzumab in Chinese patients with B-cell lymphomas. British journal of clinical pharmacology 83(7) 1446–1456. DOI:10.1111/bcp.13232 PUBMED:https://pubmed.ncbi.nlm.nih.gov/28072473

  2. Hoy, SM (2015). Obinutuzumab: a review of its use in patients with chronic lymphocytic leukaemia. Drugs 75(3) 285–296. DOI:10.1007/s40265-014-0340-3 PUBMED:https://pubmed.ncbi.nlm.nih.gov/25586272

  3. Qin, Y, et al., & Shi, Y (2018). Safety and efficacy of obinutuzumab in Chinese patients with B-cell lymphomas: a secondary analysis of the GERSHWIN trial. Cancer communications (London, England) 38(1) 31–None. DOI:10.1186/s40880-018-0300-5 PUBMED:https://pubmed.ncbi.nlm.nih.gov/29843792

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)