Oncology PopPK

Panitumumab nonlinear population PK

Reference paper ↗

A two-compartment population PK model coupling panitumumab distribution to parallel linear and saturable Michaelis–Menten elimination.

Therapeutic
Panitumumab
Modality
Monoclonal antibody
Target
EGFR / ERBB1
Disease
Cancer therapy with EGFR-targeted panitumumab
Model type
PopPK

Complete model workspace

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Parameters
6
States
4
Equations
4
Derived outputs
8

Explore this model

Choose a starting point to view its result. Adjust key model inputs when you want to explore a different outcome.

Starting configuration

Typical FFCD0904 3 mg/kg every 2 weeks with AUC

Typical FFCD0904 3 mg/kg every 2 weeks with AUC

How do linear and saturable elimination jointly shape panitumumab concentration and exposure? Explore this intervention regimen through Central panitumumab concentration, Peripheral panitumumab concentration, Linear elimination, Saturable elimination, Cumulative panitumumab exposure.

Starting result

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Starting configuration

Time: 0–70 day; step 0.25

InputDefaultAvailable range
Systemic clearance0.4 L/day0.2–0.6 L/day
Central distribution volume2.51 L1.255–3.765 L
Intercompartmental clearance0.17 L/day0.085–0.255 L/day
Peripheral distribution volume2.91 L1.455–4.365 L
Maximum elimination rate4.26 mg/day2.13–6.39 mg/day

Expected readouts

Central panitumumab concentration · Peripheral panitumumab concentration · Linear elimination · Saturable elimination · Exposure (AUC) (mg*day/L)

Adjustable model parameters

This public explorer exposes 5 curated parameters. Sign in to edit all 6 declared model parameters.

More key parameters (1)

How the model represents the biology

A two-compartment population PK model coupling panitumumab distribution to parallel linear and saturable Michaelis–Menten elimination.

How do linear and saturable elimination shape panitumumab exposure?Intravenous panitumumab enters a central pool, exchanges with a peripheral pool, and leaves through parallel linear and Michaelis-Menten elimination. Central concentration accumulates as exposure.BIOLOGY OVERVIEWHow do linear and saturable elimination shape panitumumab exposure?IV panitumumabBolus to central amountCentral exposurePanitumumab concentrationPeripheral poolReversible distributionLinear eliminationClearance-proportional lossSaturable eliminationMichaelis–Menten lossCumulative exposureCentral concentration integralPRIMARY READOUTSCentral panitumumab concentrationCentral panitumumab concen…Peripheral concentrationPeripheral concentrationLinear eliminationLinear eliminationSaturable eliminationSaturable eliminationCumulative exposureCumulative exposure

Solid arrows show modeled movement or change; two-headed arrows show reversible exchange; dashed arrows show modulation without material transfer.

Model scope: EGFR binding or occupancy, target amount or internalization, tumor response, and body-composition effects are not represented in this released runtime.

Modeled relationships (5)
  • IV panitumumab → Central exposure: IV input (flow)
  • Central exposure ↔ Peripheral pool: distribution (reversible exchange)
  • Central exposure → Linear elimination: linear CL (loss)
  • Central exposure → Saturable elimination: Vmax / Km (loss)
  • Central exposure → Cumulative exposure: integrates C (production)

Modeled relationships: IV panitumumab to Central exposure: IV input (flow); Central exposure reversibly exchanges with Peripheral pool: distribution (reversible exchange); Central exposure to Linear elimination: linear CL (loss); Central exposure to Saturable elimination: Vmax / Km (loss); Central exposure to Cumulative exposure: integrates C (production).

Primary readouts: Central panitumumab concentration; Peripheral concentration; Linear elimination; Saturable elimination; Cumulative exposure.

Found a scientific issue? Email helpdesk@unibiointelligence.com with model ID lobet_2026_panitumumab_body_composition_poppk.

Research use only — not for patient-specific prediction or dosing advice.

Ubi Biologics