Antibody-Drug Conjugate (ADC)Population PK (2-CMT ADC + 1-CMT DXd Payload)IV InfusionOncology / NSCLC

Patritumab Deruxtecan (HER3-DXd) PopPK

Indication: EGFR-mutant NSCLC after EGFR TKI and platinum therapy; HER3-directed ADC with DXd payload

Population PK simulator for patritumab deruxtecan (HER3-DXd) — HER3-directed ADC with DXd payload for EGFR-mutant NSCLC. Two-compartment ADC model with body-weight covariate (exponent 0.72) linked to one-compartment DXd payload. Standard dose 5.6 mg/kg Q3W. Based on Guo et al. 2024 CPT:PSP. Compare DXd payload exposure vs T-DXd and Dato-DXd.

Drug Overview

Clinical Context

Molecular Target
HER3 (ERBB3)
Drug Class
Antibody-Drug Conjugate (ADC)
Therapeutic Area
Oncology / NSCLC
Indication
EGFR-mutant NSCLC after EGFR TKI and platinum therapy; HER3-directed ADC with DXd payload
Route of Administration
IV Infusion

Model Information

Model Type
Population PK (2-CMT ADC + 1-CMT DXd Payload)

This simulator was built from published pharmacometric literature using PKPDBuilder's AI-powered model extraction pipeline.

Pharmacokinetic Parameters

Additional Parameters

ParameterValue
k120.18
k210.28
ADC CL0.38
DXd Vd580
Standard Dose5.6
DXd Payload CL45
ADC V1 (Central)3.2
BW Exponent on CL0.72
ADC V2 (Peripheral)1.8
Payload Release Rate (kr)0.012

Parameters sourced from published population pharmacokinetic models. Values represent typical population estimates; individual patient parameters may vary.

About This Simulator

This interactive pharmacokinetic simulator for Patritumab Deruxtecan (HER3-DXd) allows you to explore concentration-time profiles under different dosing scenarios. The underlying Population PK (2-CMT ADC + 1-CMT DXd Payload) model characterizes the pharmacokinetics of this antibody-drug conjugate (adc) following iv infusion administration.

Use the simulator to visualize key exposure metrics including AUC (area under the curve), Cmax (peak concentration), and Ctrough (trough concentration).

Built with PKPDBuilder — an AI-powered platform that transforms published pharmacometric literature into interactive, deployable Shiny applications. No coding required.

Frequently Asked Questions

What is the Patritumab Deruxtecan (HER3-DXd) PK simulator?

This is a free, interactive pharmacokinetic simulator for Patritumab Deruxtecan (HER3-DXd) used in EGFR-mutant NSCLC after EGFR TKI and platinum therapy; HER3-directed ADC with DXd payload. It allows researchers, pharmacologists, and students to explore concentration-time profiles, dosing regimens, and exposure metrics based on published population PK models.

What drug class does Patritumab Deruxtecan (HER3-DXd) belong to?

Patritumab Deruxtecan (HER3-DXd) is classified as a Antibody-Drug Conjugate (ADC) that targets HER3 (ERBB3). It is used in the Oncology / NSCLC therapeutic area.

What route of administration does this model simulate?

This simulator models IV Infusion administration of Patritumab Deruxtecan (HER3-DXd). The pharmacokinetic parameters (absorption rate, bioavailability, volume of distribution) are specific to this route.

What type of PK model is used?

This simulator uses a Population PK (2-CMT ADC + 1-CMT DXd Payload) model. This model characterizes the time-course of drug concentrations following dosing.

Is this simulator free to use?

Yes, all PKPDBuilder simulators are completely free. They are built from published pharmacokinetic literature and are intended for research and educational purposes. No login is required to run simulations.

Can I use this for clinical dosing decisions?

No. This simulator is for research and educational purposes only. It should not be used for clinical decision-making or patient dosing. Always consult the prescribing information and clinical pharmacology guidelines for therapeutic drug use.

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⚠️ Disclaimer

This simulator is for research and educational purposes only. It is not intended for clinical decision-making, patient dosing, or therapeutic drug monitoring. Pharmacokinetic parameters are derived from published literature and represent population-level estimates. Individual patient pharmacokinetics may differ significantly. Always consult approved prescribing information and qualified healthcare professionals for clinical decisions.

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